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Prostatitis: Causes, symptoms & Treatments

Prostatitis is an inflammation or infection of the prostate gland. It affects at least half of all men at some time in their lives. Having this condition does not increase your risk of any other prostate disease.

Symptoms

  • Trouble passing urine or pain when passing urine
  • A burning or stinging feeling when passing urine
  • Strong, frequent urge to pass urine, even when there is only a small amount of urine
  • Chills and high fever
  • Low back pain or body aches
  • Pain low in the belly, groin, or behind the scrotum
  • Rectal pressure or pain
  • Urethral discharge with bowel movements
  • Genital and rectal throbbing
  • Sexual problems and loss of sex drive
  • Blocked urine
  • Painful ejaculation

Prostatitis is not contagious. It is not spread through sexual contact. Your partner cannot catch this infection from you.

Several tests, such as DRE and a urine test, can be done to see if you have prostatitis. Getting the right diagnosis of your exact type of prostatitis is the key to getting the best treatment. Even if you have no symptoms, you should follow your doctor’s suggestion to complete treatment.

Types

There are four types of prostatitis:

Acute bacterial prostatitis

This infection comes on suddenly (acute) and is caused by bacteria. Symptoms include severe chills and fever. There is often blood in the urine.

Treatment: Most cases can be cured with a high dose of antibiotics, taken for 7 to 14 days, and then lower doses for several weeks. You may also need drugs to help with pain or discomfort.

Chronic bacterial prostatitis

Also caused by bacteria, this condition doesn’t come on suddenly, but it can be bothersome. The only symptom you may have is bladder infections that keep coming back. The cause may be a defect in the prostate that lets bacteria collect in the urinary tract.

Treatment: Antibiotic treatment over a longer period of time is best for this type.

Chronic prostatitis or chronic pelvic pain syndrome

This disorder is the most common but least understood form of the disease. Found in men of any age from late teens to elderly, its symptoms go away and then return without warning. There can be pain or discomfort in the groin or bladder area.

Treatment: There are several different treatments for this problem, based on your symptoms. These include antibiotics and other medicines, such as alpha-blockers. Alpha-blockers relax muscle tissue in the prostate to make passing urine easier.

Asymptomatic inflammatory prostatitis

You usually don’t have symptoms with this condition. It is often found when your doctor is looking for other conditions like infertility or prostate cancer. If you have this problem, often your PSA test (see The PSA Test) will show a higher number than normal. It does not necessarily mean that you have cancer.

Treatment: Men with this condition are usually given antibiotics for 4 to 6 weeks, and then have another PSA test.

 

Propeller flaps for leg reconstruction: How it construct in patients

Reverse sural artery fasciocutaneous flap has become a workhorse for the reconstruction of distal leg soft tissue defects. When its use is not feasible, perforator-based propeller flap offers a better, easier, faster, and cheaper alternative to free flap. We present our experience with two men both aged 34 years who sustained Gustilo 3B injuries from gunshot. The donor area for reversed sural artery flap was involved in the injuries. They had early debridement, external fixation, and wound coverage with perforator-based propeller flaps. The donor sites were covered with skin graft. All flaps survived. There were minor wound edge ulcers due to the pressure of positioning that did not affect flap survival and the ulcers healed with conservative management. Perforator-based propeller flap is a versatile armamentarium for reconstruction of soft tissue defects of the distal leg in resource-constrained settings, especially when the donor area for a reverse flow sural flap artery is involved in the injury.

INTRODUCTION

Reconstruction of soft tissue defects in the distal third of the leg pose challenges for reconstruction as a result of the paucity of donor tissue, bony prominence at the medial and lateral malleolus, and relatively poor blood supply of the region.Random pattern flaps raised in the leg are limited in reliability, size, reach, and arc-of-rotation. Most major injuries of the distal leg are associated with significant soft tissue defects because the tibia is mostly subcutaneous anteromedially. There is also less muscle bulk around its lower third.

Reverse sural artery fasciocutaneous flap has become a workhorse for the reconstruction of distal leg soft tissue defects in settings with limited resources. Its use obviates the need for sophisticated equipment, extended operative time, and super specialized training. Revere sural artery flap is a relatively easy and fast method of transferring a large amount of tissue. It allows for good hemostasis, and it has a short learning curve.

When the vascular supply to this flap is injured as found in our patients, reliable options for reconstruction in the distal third of the leg becomes limited.

Free tissue transfer would have been another modality to choose; however, microsurgical skills, specialized equipment, cost, steep learning curve, and prolonged operating time required for this modality reduces its feasibility in our practice setting and even outside tertiary care centers in more developed countries.

Perforator-based flaps address these problems. They afford speed, simplicity, color and texture match, lower cost, and allow greater arc of movement. Its applicability is possible in most parts of the body. Successful outcomes have been described in the axilla, periolecranon, forearm, lower extremity, hand and trunk. In spite of the versatility of perforator-based flaps, literature search reveals that report of its use is sparse from our practice setting.

We therefore present our experience with the use of three (tibioperoneal system) perforator-based propeller flaps in the reconstruction of distal leg defects following gunshot injuries. Perforator-based propeller flap provides a reliable option for resurfacing soft tissue defects when other options are not feasible.

Anatomy of distal leg perforators

Perforators are small diameter vessels that originate from a main pedicle and perforate the fascia or muscle to reach the skin. The development of flaps based on perforators has followed the understanding of the blood supply from a source artery to the skin.[8,9] Anatomical studies have revealed that they emerge from the crural fascia in four longitudinal rows within the intermuscular septa that border the compartments of the lower leg and the tibia. They are grouped into clusters of perforators with consistent distance proximal to the intermalleolar line. In the leg, there are anterior tibial artery perforators; posterior tibial artery perforators, peroneal artery perforators, and sural artery perforators.[8]

CASE REPORTS

Two men both aged 34–year-old of different addresses at different incidences, were shot in the distal aspect of the left leg.

Case 1

The first patient was attacked by armed robber; he sustained Gustilo 3B open fractures with two soft tissue defects: A lateral one measuring 12 cm × 7 cm and a medial defect 14 cm × 6 cm [Figure 1] with injury to the recurrent sural artery precluding the use of the reversed sural artery flap for wound coverage. The distal part of the tibia and injured tendons were left exposed in the wound bed. He had initial wound debridement and application of external fixators to immobilize his fractures. He subsequently had wound coverage with two perforator-based propeller flaps raised from the medial and lateral aspect of the leg [Figure 2]. The secondary defects were covered with split-thickness skin graft. During the postoperative period, he developed seroma under the lateral flap which was drained and did not have any adverse effect on flap survival. He also developed a Grade 2 pressure ulcer on the lateral edge of the wound due to limb positioning. This healed without surgical intervention. Skin graft take was 100%. Figure 3 shows the surgical outcome six weeks postoperatively.

Figure 1

Figure 1
Preoperative picture before debridement
Figure 2

Figure 2
Immediate postoperative picture
Figure 3

Figure 3
Follow-up picture 6 weeks postoperatively

Case 2

The second patient was shot during an argument; he sustained Gustilo 3B open fractures. The entry wound was quite small, but the exit wound located posteriorly measured 14 cm × 11 cm and a large portion of the Achilles tendon was exposed. The sural artery was found severed in the wound [Figure 4]. He had wound debridement, fracture reduction, and immobilization with an external fixator. A perforator-based propeller flap was raised to cover the wound and split thickness skin graft was applied to the secondary defect [Figure 5]. Flap survived without any area of loss [Figure 6]. The pins of the external fixator became loosened the 10th postoperative day, and the wound had to be manipulated to tighten the loose component. He developed hematoma in the wound after the procedure. This was drained with removal of the staples around the hematoma and the wound healed satisfactorily thereafter. Skin graft take was 100%.

Figure 4

Figure 4
Preoperative picture showing exposed Achilles tendon. The cavitation effect of the gunshot damaged the sural artery
Figure 5

Figure 5
Immediate postoperative picture
Figure 6

Figure 6
Fifth postoperative day

Flap design and surgical technique

Perforators in the proposed donor tissue close to the defect were located preoperatively using handheld Doppler (probe) and marked on the skin using methylene blue [Figure 7]. The flaps were then designed like blades of a propeller adjacent to the defects. The proximal end of the flap to the targeted perforator is made equidistant from the distal end of the defect to the perforator.

Figure 7

Figure 7
Preoperative planning showing the flap outline. Identified perforators were marked as x on the outline

The flap sizes were made to be 0.5 cm more than the size of the defect to be covered to aid closure without tension.

An exploratory skin incision was made and carried through to include the deep fascia. Through this incision, blunt dissection in the subfascial plane was done to isolate the perforator. As soon as the adequacy of the perforator is assured, the other incisions were completed, and other perforators that would not be used were ligated. Fascial strands were released to allow for mobilization of the flaps and to avoid tension on the pedicle during the transfer. The flaps were rotated 180° into place like a propeller blade avoiding kinking of the perforator. Hemostasis was secured with diathermy and tourniquet without exsanguination was used for the first patient, but diathermy and ligatures were used for the second patient. Flaps were inset and secured using skin staples.

The sizes of the secondary defects were reduced by suturing and the remaining defect skin grafted. Primary closure was not possible in all the donor sites due to the size of flaps harvested. Bedside, flap monitoring was achieved via a window created within the dressing to examine the flaps.

Pediatric Stroke : Symptoms, causes & Treatments

Symptoms:

Because people do not think about newborns and children having strokes, they are not often recognized or treated properly. Another challenge with newborns is that they cannot communicate symptoms that are not readily visible.

The common stroke warning signs used to identify stroke in adults can also be used to identify strokes in children.  But, there are some specific symptoms that you should look for in children depending on their age.

In newborns and infants

  • Seizures.
  • Extreme sleepiness.
  • Tendency to use only one side of their body.

In children and teens

  • Severe headaches
  • Vomiting
  • Sleepiness
  • Dizziness
  • Loss of balance or coordination

CAUSES:

While high blood pressure, an irregular heartbeat and a hardening of the arteries are common causes of adult strokes, they are rare in children. Common risk factors for stroke in children include:

  • Congenital heart defects
  • Sickle-cell disease
  • Immune disorders
  • Diseases of the arteries
  • Abnormal blood clotting
  • Head or neck trauma
  • Maternal history of infertility
  • Maternal infection in the fluid surrounding an unborn baby
  • Premature rupture of membrane during pregnancy
  • Pregnancy related high blood pressure in the mother

TREATMENTS:

Children usually recover better from strokes than adults do because their brains are still growing. However, children can experience permanent complications from stroke, such as seizures, weakness, and vision problems.

Treatment for pediatric stroke depends on the specific cause. Some common treatments used with adults are not appropriate for young children and infants. One of the best treatments for ischemic strokes for adults is tPA, or tissue plasminogen activator, a drug that dissolves blood clots.

With children under 18, use of tPA is controversial and currently limited to clinical trials. Further studies on safety and benefits of this treatment are necessary. Rehabilitation methods with pediatric stroke survivors are also not clear and require further clinical trials.

Current treatments for pediatric stroke include:

  • Supportive care to maintain normal body temperature, proper hydration, and normal blood sugar levels.
  • Controlling high blood pressure.
  • Detecting and treating seizures with EEG monitoring and anticonvulsant medication.
  • Managing intracranial pressure.
  • Blood transfusions for children with sickle-cell disease.
  • Antithrombotic therapy, which refers to medications used to prevent blood clots from forming or growing, is used in children but generally not infants.
  • Surgery related to hemorrhagic stroke (and less commonly, ischemic stroke) is sometimes performed to relieve pressure on the brain.

 

Systemic Lupus Erythematosus (SLE): Symtoms, causes & Treatments

Common symptoms of LUPUS are:
  • severe fatigue.
  • joint pain.
  • joint swelling.
  • headaches.
  • a rash on the cheeks and nose, which is called a “butterfly rash”
  • hair loss.
  • anemia.
  • blood-clotting problems.

What Is Lupus?

Lupus is an autoimmune disease whereby a misdirected immune system leads to inflammation and injury to one’s own body tissues.

Signs of Lupus

Lupus can involve many different parts of the body, including:

  • Skin
  • Joints
  • Heart
  • Lungs
  • Kidneys
  • Brain

There is no specific cure for lupus, but treatments are effective at minimizing lupus damage and improving function. Approximately 80% of lupus patients are women.

Picture of Systemic Lupus Erythematosus 1

Lupus Symptoms: Joint Pain

Though the first signs of the lupus disease can be rash, there are often pains in the muscles and joints. Both sides of the body tend to be affected. Hands, wrists, knees, and feet are commonly affected. The joints can become swollen, warm, and have limited range of motion.

Lupus Symptoms: Butterfly Rash

A classic lupus rash involves the cheeks and over the bridge of the nose. This is referred to as a “butterfly-shaped” lupus rash. It is also common for the skin to be very sensitive to burning and irritation after sun exposure. This is referred to as photosensitivity.

Lupus Symptoms: Nail Changes

Lupus rash can cause a ruddy discoloration of the backs of the hands and fingers. There can also be poor circulation to the nail beds that leads to irregularities of the fingernails. Inflammation at the nail bed can cause swelling and puffiness.

What are risk factors and causes of systemic lupus erythematosus? Is lupus contagious? Is lupus hereditary?

The precise reason for the abnormal autoimmunity that causes lupus is not known. Inherited genes, viruses, ultraviolet light, and certain medications may all play some role.

Lupus is not caused by an infectious microorganism and is not contagious from one person to another.

Genetic factors increase the tendency of developing autoimmune diseases, and autoimmune diseases such as lupus, rheumatoid arthritis, and autoimmune thyroid disorders are more common among relatives of people with lupus than the general population. Moreover, it is possible to have more than one autoimmune disease in the same individual. Therefore, “overlap” syndromes of lupus and rheumatoid arthritis, or lupus and scleroderma, etc., can occur.

Some scientists believe that the immune system in lupus is more easily stimulated by external factors like viruses or ultraviolet light. Sometimes, symptoms of lupus can be precipitated or aggravated by only a brief period of sun exposure.

It also is known that some women with SLE can experience worsening of their symptoms prior to their menstrual periods. This phenomenon, together with the female predominance of SLE, suggests that female hormones play an important role in the expression of SLE. This hormonal relationship is an active area of ongoing study by scientists.

Research has demonstrated evidence that a key enzyme’s failure to dispose of dying cells may contribute the development of SLE. The enzyme, DNase1, normally eliminates what is called “garbage DNA” and other cellular debris by chopping them into tiny fragments for easier disposal. Researchers turned off the DNase1 gene in mice. The mice appeared healthy at birth, but after six to eight months, the majority of mice without DNase1 showed signs of SLE. Thus, a genetic mutation in a gene that could disrupt the body’s cellular waste disposal may be involved in the initiation of SLE.

What is the treatment for systemic lupus?

There is no permanent cure for SLE. The goal of treatment is to relieve symptoms and protect organs by decreasing inflammation and/or the level of autoimmune activity in the body. The precise treatment is decided on an individual basis. Many people with mild symptoms may need no treatment or only intermittent courses of anti-inflammatory medications. Those with more serious illness involving damage to internal organ(s) may require high doses of corticosteroids in combination with other medications that suppress the body’s immune system.

People with SLE need more rest during periods of active disease. Researchers have reported that poor sleepquality was a significant factor in developing fatigue in people with SLE. These reports emphasize the importance for people and physicians to address sleep quality and the effect of underlying depression, lack of exercise, and self-care coping strategies on overall health. During these periods, carefully prescribed exercise is still important to maintain muscle tone and range of motion in the joints.

To protect from sun sensitivity, sunscreens, sun avoidance, and sun protection clothing are used. Certain types of lupus rash can respond to topical cortisone medications.

Nonsteroidal anti-inflammatory drugs (NSAIDs) are helpful in reducing inflammation and pain in muscles, joints, and other tissues. Examples of NSAIDs include aspirin, ibuprofen(Motrin), naproxen (Naprosyn), and sulindac (Clinoril). Since the individual response to NSAIDs varies, it is common for a doctor to try different NSAIDs to find the most effective one with the fewest side effects. The most common side effects are stomach upset, abdominal pain, ulcers, and even ulcer bleeding. NSAIDs are usually taken with food to reduce side effects. Sometimes, medications that prevent ulcers while taking NSAIDs, such as misoprostol (Cytotec), are given simultaneously.

Corticosteroids are more potent than NSAIDs in reducing inflammation and restoring function when the disease is active. Corticosteroids are particularly helpful when internal organs are affected. Corticosteroids can be given by mouth, injected directly into the joints and other tissues, or administered intravenously. Unfortunately, corticosteroids have serious side effects when given in high doses over prolonged periods, and the doctor will try to monitor the activity of the disease in order to use the lowest doses that are safe. Side effects of corticosteroids include weight gain, thinning of the bones and skin, infection, diabetes, facial puffiness, cataracts, and death (necrosis) of the tissues in large joints.

Hydroxychloroquine (Plaquenil) is an antimalarial medication found to be particularly effective for SLE people with fatigue, skin involvement, and joint disease. Consistently taking Plaquenil can prevent flare-ups of lupus. Side effects are uncommon but include diarrhea, upset stomach, and eye-pigment changes. Eye-pigment changes are rare but require monitoring by an ophthalmologist (eye specialist) during treatment with Plaquenil. Researchers have found that Plaquenil significantly decreased the frequency of abnormal blood clots in people with systemic lupus. Moreover, the effect seemed independent of immune suppression, implying that Plaquenil can directly act to prevent the blood clots. This fascinating study highlights an important reason for people and doctors to consider Plaquenil for long-term use, especially for those SLE people who are at some risk for blood clots in veins and arteries, such as those with phospholipid antibodies (cardiolipin antibodies, lupus anticoagulant, and false-positive venereal disease research laboratory test). This means not only that Plaquenil reduces the chance for re-flares of SLE, but it can also be beneficial in thinning the blood to prevent abnormal excessive blood clotting. Plaquenil is commonly used in combination with other treatments for lupus.

For resistant skin disease, other antimalarial drugs, such as chloroquine (Aralen) or quinacrine, are considered and can be used in combination with hydroxychloroquine. Alternative medications for skin disease include dapsone and retinoic acid (Retin-A). Retin-A is often effective for an uncommon wart-like form of lupus skin disease. For more severe skin disease, immunosuppressive medications are considered as described below.

Medications that suppress immunity (immunosuppressive medications) are also called cytotoxic drugs. They are sometimes referred to as chemotherapy because they are also used to treat cancer, generally in much higher doses than those used to treat lupus. Immunosuppressive medications are used for treating people with more severe manifestations of SLE, such as damage to internal organ(s). Examples of immunosuppressive medications include methotrexate (Rheumatrex, Trexall), azathioprine (Imuran), cyclophosphamide (Cytoxan), chlorambucil (Leukeran), and cyclosporine (Sandimmune). All immunosuppressive medications can seriously depress blood-cell counts and increase risks of infection and bleeding. Immunosuppressive medications may not be taken during pregnancy or conception because of risk to the fetus. Other side effects are specific for each drug. For examples, methotrexate can cause liver toxicity, while cyclosporine can impair kidney function.

In recent years, mycophenolate mofetil (CellCept) has been used as an effective medication for lupus, particularly when it is associated with kidney disease. CellCept has been helpful in reversing active lupus kidney disease (lupus renal disease) and in maintaining remission after it is established. Its lower side-effect profile has advantage over traditional immune-suppression medications.

In SLE patients with serious brain (lupus cerebritis) or kidney disease (lupus nephritis), plasmapheresis is sometimes used to remove antibodies and other immune substances from the blood to suppress immunity. Plasmapheresis is a process of removing blood and passing the blood through a filtering machine, then returning the blood to the body with its antibodies removed. Rarely, people with SLE can develop seriously low platelet levels, thereby increasing the risk of excessive and spontaneous bleeding. Since the spleen is believed to be the major site of platelet destruction, surgical removal of the spleen is sometimes performed to improve platelet levels. Other treatments have included plasmapheresis and the use of male hormones.

Plasmapheresis has also been used to remove certain harmful proteins (cryoglobulins) that can lead to vasculitis. End-stage kidney damage from SLE requires dialysis and/or a kidney transplant.

Fibromyalgia: Symptoms, causes & Treatments

Fibromyalgia syndrome affects the muscles and soft tissue. Symptoms include chronic muscle pain, fatigue, sleep problems, and painful tender points or trigger points, which can be relieved through medications, lifestyle changes and stress management.

 What Are the Symptoms of Fibromyalgia?

Symptoms of fibromyalgia include:

  • Chronic muscle pain, muscle spasms, or tightness
  • Moderate or severe fatigue and decreased energy
  • Insomnia or waking up feeling just as tired as when you went to sleep
  • Stiffness upon waking or after staying in one position for too long
  • Difficulty remembering, concentrating, and performing simple mental tasks (“fibro fog”)
  • Abdominal pain, bloating, nausea, and constipation alternating with diarrhea (irritable bowel syndrome)
  • Tension or migraine headaches
  • Jaw and facial tenderness
  • Sensitivity to one or more of the following: odors, noise, bright lights, medications, certain foods, and cold
  • Feeling anxious or depressed
  • Numbness or tingling in the face, arms, hands, legs, or feet
  • Increase in urinary urgency or frequency (irritable bladder)
  • Reduced tolerance for exercise and muscle pain after exercise
  • A feeling of swelling (without actual swelling) in the hands and feet

When it comes to fibromyalgia treatments, there are drugs, alternative remedies, and lifestyle habits that may help decrease pain and improve sleep. Your fibromyalgia specialist may prescribe pain medication or antidepressants to help treat the pain, fatigue, depression, and anxietythat comes with the disease. In addition, your doctor may recommend physical therapy, moist heat, regular aerobic exercise, relaxation, and stress reduction to help you self-manage your symptoms.

There is no one “pill” that treats or cures fibromyalgia. A multidisciplinary approach that uses both medication and alternative or lifestyle strategies seems to work best to treat fibromyalgia symptoms.

Is Fibromyalgia Pain Similar to Arthritis Pain?

Fibromyalgia can cause symptoms similar to arthritis, bursitis, and tendinitis. Consequently, some experts group fibromyalgia with arthritis and related disorders. The pain associated with these other conditions is typically localized to a single area, while the pain and stiffness of fibromyalgia are very widespread and consists of deep muscle pain, morning stiffness, and painful tender points, making it difficult to exercise or be physically active.

 

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How Is Fibromyalgia Fatigue Treated?

Along with deep muscle pain and painful tender points, fatigue is a key symptom of fibromyalgia and it can be debilitating. Not only do you feel exhausted and weak, but bed rest does not seem to help. Many people with fibromyalgia report sleeping eight to 10 hours at night and feeling as if they haven’t slept at all.

Some drugs may help ease the fatigue associated with fibromyalgia. In addition, aerobic exercise can help ease fatigue, minimize pain, improve quality of sleep, and improve mood.

 

How Does Exercise Help Fibromyalgia Symptoms?

Numerous studies show that exercise is one of the most important treatments for fibromyalgia. Many people with fibromyalgia are are not physically fit. They avoid exercise because they fear increased pain. Yet aerobic or conditioning exercise can actually help relieve pain and depression.

Regular exercise increases the body’s production of endorphins, natural painkillers that also boost mood. Starting slowly and gradually increasing the duration and intensity of exercise can help you enjoy the benefits of exercise without feeling more pain.

Vasculitis: Symptoms, causes & Tratments

Vasculitis is a general term for a group of uncommon diseases that feature inflammation of the blood vessels. The blood vessels of the body are referred to as the vascular system. The blood vessels are comprised of arteries that pass oxygen-rich blood to the tissues of the body and veins that return oxygen-depleted blood from the tissues to the lungs for oxygen. Vasculitis is characterized by inflammation in and damage to the walls of various blood vessels.

Each of the vasculitis diseases is defined by certain patterns of distribution of blood vessel involvement, particular organ involvement, and laboratory test abnormalities. As a group, these diseases are referred to as vasculitides.

The word vasculitis is derived from the Latin “vasculum”, vessel + “- itis”, inflammation. Another term for vasculitis is angiitis. When arteries are the inflamed blood vessels, the condition is also referred to as arteritis. When the veins are inflamed, it is referred to as venulitis.

What causes vasculitis, and what are examples of diseases with vasculitis?

The actual cause of these vasculitis diseases is usually not known. However, immune system abnormality and inflammation of blood vessels are common features. Each form of vasculitis has its own characteristic pattern of symptoms, much of which depends on what particular organs are affected.

Examples of vasculitis include:

  • Kawasaki disease,
  • Behçet’s disease,
  • polyarteritis nodosa,
  • Wegener’s granulomatosis,
  • Cryoglobulinemia,
  • Takayasu’s arteritis,
  • Churg-Strauss syndrome,
  • Giant cell arteritis (temporal arteritis), and
  • Henoch-Schönlein purpura.

 

What causes vasculitis, and what are examples of diseases with vasculitis?

The actual cause of these vasculitis diseases is usually not known. However, immune system abnormality and inflammation of blood vessels are common features. Each form of vasculitis has its own characteristic pattern of symptoms, much of which depends on what particular organs are affected.

Examples of vasculitis include:

  • Kawasaki disease,
  • Behçet’s disease,
  • polyarteritis nodosa,
  • Wegener’s granulomatosis,
  • Cryoglobulinemia,
  • Takayasu’s arteritis,
  • Churg-Strauss syndrome,
  • Giant cell arteritis (temporal arteritis), and
  • Henoch-Schönlein purpura.

Vasculitis can also accompany:

  • Infections (such as hepatitis B),
  • Exposure to chemicals (such as amphetamines and cocaine),
  • Medications,
  • Cancers (such as lymphomas and multiple myeloma), and
  • Rheumatic diseases (such as rheumatoid arthritis and systemic lupus erythematosus

Treatments:

The treatment of the various forms of vasculitis is based on the severity of the illness and the organs involved. Treatments are generally directed toward stopping the inflammation and suppressing the immune system. Typically, cortisone-related medications, such as prednisone , are used. Additionally, other immune suppression drugs, such as cyclophosphamide (Cytoxan) and others, are considered. Additionally, affected organs (such as the heart or lungs) may require specific medical treatment when the disease is active.

The management of vasculitis is an evolving field in medicine. The ideal programs for monitoring and treatment will continue to improve as disease patterns and causes are defined by medical research.

Craniosynostosis : Symptoms, Causes & Treatments

Craniosynostosis (kray-nee-o-sin-os-TOE-sis) is a birth defect in which one or more of the joints between the bones of your baby’s skull close prematurely, before your baby’s brain is fully formed. When your baby has craniosynostosis, his or her brain can’t grow in its natural shape and the head is misshapen.

Craniosynostosis can affect one or more of the joints in your baby’s skull. In some cases, craniosynostosis is associated with an underlying brain abnormality that prevents the brain from growing properly.

Treating craniosynostosis usually involves surgery to separate the fused bones. If there’s no underlying brain abnormality, the surgery allows your baby’s brain adequate space to grow and develop.

Craniosynostosis symptoms:

Signs of craniosynostosis include:

  • A misshapen skull, with the shape depending on which of the cranial sutures are affected
  • An abnormal feeling or disappearing “soft spot” (fontanel) on your baby’s skull
  • Slow or no growth of the head as your baby grows
  • Development of a raised, hard ridge along affected sutures
  • Increased pressure within the skull (intracranial pressure)

The signs of craniosynostosis may not be noticeable at birth, but they become apparent during the first few months of your baby’s life.

Craniosynostosis types and characteristics

There are many different types of craniosynostosis. The term given to each type depends on what sutures are affected. Some of the most common types of craniosynostosis are:

  • Sagittal synostosis (scaphocephaly). Premature fusion of the suture at the top of the head (sagittal suture) forces the head to grow long and narrow, rather than wide. Scaphocephaly is the most common type of craniosynostosis.
  • Coronal synostosis (anterior plagiocephaly). Premature fusion of a coronal suture — one of the structures that run from each ear to the sagittal suture on top of the head — may force your baby’s forehead to flatten on the affected side. It may also raise the eye socket and cause a deviated nose and slanted skull.
  • Bicoronal synostosis (brachycephaly). When both of the coronal sutures fuse prematurely, your baby may have a flat, elevated forehead and brow.

Causes:

Craniosynostosis is often classified as nonsyndromic or syndromic. Nonsyndromic craniosynostosis is the most common type of craniosynostosis, and its cause is unknown.

However, syndromic craniosynostosis is a complication caused by certain genetic syndromes, such as Apert syndrome, Pfeiffer syndrome and Crouzon syndrome, which can affect your baby’s skull development. Besides craniosynostosis, other conditions also may accompany such syndromes — including hand and foot deformities, dental abnormalities, and heart problems.

 

Treatments and drugs:

Mild cases of craniosynostosis — those that involve only one suture and no underlying syndrome — may require no treatment. Skull abnormalities may become less obvious as your baby grows and develops hair. Or your doctor might recommend a specially molded helmet to help reshape your baby’s head and allow room for your baby’s brain growth.

Surgery:

For most babies, however, surgery is the primary treatment for craniosynostosis. The type and timing of surgery depend on the type of craniosynostosis and whether there’s an underlying syndrome that needs treatment.

The purpose of surgery is to relieve pressure on the brain, create room for the brain to grow normally and improve your child’s appearance. A team that includes a specialist in surgery of the head and face (craniofacial surgeon) and a specialist in brain surgery (neurosurgeon) often performs the procedure.

  • Traditional surgery. The surgeon makes an incision in your baby’s scalp and cranial bones, then reshapes the affected portion of the skull. Sometimes plates and screws, often made of material that is absorbed over time, are used to hold the bones in place. Surgery, which is performed during general anesthesia, usually takes hours.After surgery, your baby remains in the hospital for at least three days. Some children may require a second surgery later because the craniosynostosis recurs. Also, children with facial deformities often require future surgeries to reshape their faces.
  • Endoscopic surgery. This less invasive form of surgery isn’t an option for everyone. But in certain cases, the surgeon may use a lighted tube (endoscope) inserted through one or two small scalp incisions over the affected suture. The surgeon then opens the suture to enable your baby’s brain to grow normally. Endoscopic surgery usually takes about an hour, causes less swelling and blood loss, and shortens the hospital stay, often to one day after surgery.

If your baby has an underlying syndrome, your doctor may recommend regular follow-up visits after surgery to monitor head growth and check for increased intracranial pressure. Head growth will be routinely monitored at well-child visits.

Aneurysm: Symptoms, treatment & Prevention

What is an aneurysm?

An aneurysm is an arterial condition in which the wall of an artery weakens, creating a bulge, or distension of the artery.

Diagrams of arteries and blood flow.
A comparison between an artery with an aneurysm and two different types of artery. Note the cross-section showing a thinner artery wall in the third diagram for aneurysm, compared with normal and narrowed arteries.

An aneurysm can occur in important arteries such as those supplying blood to the brain, and the aorta; the large artery that originates at the left ventricle of the heart and passes down through the chest and abdominal cavities.

The normal diameter of the aorta is around 0.8 inches. This width can bulge to beyond 2 inches with an aneurysm, a width that would typically necessitate surgical treatment.

An aneurysm can also occur in peripheral arteries – usually behind the knee (popliteal aneurysms) – although rupture of these is relatively uncommon.

The two most important common locations for aneurysms are:

  • In the artery directly leaving the heart – an aortic aneurysm (including thoracic and, further down, abdominal aortic aneurysms)
  • In an artery in the brain – a cerebral aneurysm.

Thoracic aortic aneurysm is often abbreviated to TAA, and abdominal aortic aneurysm to AAA. Brain aneurysms are often termed intracranial aneurysms, as well as “berry aneurysms” on account of their size and shape.

Two other examples of aneurysm are mesenteric artery aneurysm (affecting the artery supplying the intestines of the gut) and splenic artery aneurysm (occurring in the spleen, an abdominal organ).

Symptoms of aneurysm:

Most aneurysms do not themselves cause any symptoms.

Even if an aneurysm does not rupture, however, a large aneurysm may obstruct circulation to other tissues. An aneurysm can also contribute to the formation of blood clots that then obstruct smaller blood vessels, potentially causing ischemic stroke or other serious problems; this is known as thromboembolism.

Back pain can be a symptom of an aneurysm although most aneurysms are asymptomatic.

Abdominal aneurysms are sometimes associated with symptoms if they grow rapidly. Some people report abdominal or lower back pain, or a pulsating sensation in the abdomen.

Similarly, thoracic aneurysms can cause symptoms by affecting nearby tissues, including nerves and other blood vessels.

If an aneurysm compresses the laryngeal or vagus nerve, it can cause chest or back pain and symptoms such as coughing, wheezing and difficulty swallowing. Compression of the coronary artery can also cause chest pain.

Otherwise, aneurysms tend to produce symptoms only when there are complications such as rupture.

Symptoms can also be related to the cause of the aneurysm rather than the aneurysm itself. In the case of infection or vasculitis (blood vessel inflammation), for example, there may be fever, malaise or weight loss.

Complications of aneurysm

If an aneurysm has remained undetected, the first sign of it could be when there is a complication – in particular, a rupture – with symptoms resulting from this rather than the aneurysm itself.

The majority of people living with an aneurysm do not suffer any of the complications in the following list. Managing the risk factors is important, however, because all of these possibilities are serious.

Complications of aneurysm include:

Image of a stroke.
Brain aneurysm can lead to subarachnoid hemorrhage; a symptom of this stroke bleed is a sudden extreme headache.
  • Thromboembolism – depending on where the clot has traveled to, thromboembolism can cause pain in the extremities or the abdomen. If a clot travels to the brain, it can cause a stroke
  • Dissection of the aorta – see below for more detail
  • Severe chest and/or back pain – if a silent or diagnosed aortic aneurysm in the chest ruptures, severe chest or back pain may arise. Such symptoms may help hospital medical staff diagnose an aneurysm.
  • Angina – certain types of aneurysm can lead to angina, another type of chest pain; the pain is related to narrowed arteries supplying the heart itself (causing myocardial ischemia and possibly heart attack).
  • Sudden extreme headache – if a brain aneurysm leads to subarachnoid hemorrhage (a kind of stroke), the main symptom is sudden extreme headache; often so severe that it is unlike any previous experience of head pain.
  • Other symptoms – with any aneurysm rupture there may be pain, low blood pressure, a rapid heart rate, and light-headedness.

Again, most people with an aneurysm will not suffer any of these complications, and the risk can be reduced by taking preventive steps.

Treatments for aneurysm

Not all cases of unruptured aneurysm need active treatment, but when an aneurysm ruptures, emergency surgery is needed.

More details follow for the treatment options against the two main types of aneurysm.

Aortic aneurysm treatment options

An aortic aneurysm, whether abdominal or thoracic, may not need any active treatment and instead may just be monitored regularly. Medications and preventive measures may form part of conservative management or they may accompany active surgical treatment – through open or endovascular surgery.

Aortic aneurysm surgery can be performed as open surgery or as endovascular surgery.

Aneurysms that rupture require emergency surgery. Without immediate repair, a ruptured aneurysm is always fatal in the thoracic aorta, and almost always fatal in the abdominal aorta.

The decision to operate on an unruptured aneurysm in the aorta depends on a number of factors related to the individual patient, as well as to features of the aneurysm itself:

  • Individual factors – age, general health, coexisting conditions and personal choice
  • The aneurysm’s characteristics – size relative to location in the thorax or abdomen and the rate of growth
  • Other factors – chronic abdominal pain or risk of thromboembolism may make surgery a good option.

An aortic aneurysm that has a larger diameter (about 2 inches or 5 cm) is more likely to prompt a recommendation of surgery, as is an aneurysm which is growing more quickly (a little less than 1/4 inch over the last 6-12 months).

For both elective unruptured and emergency ruptured cases, surgery can take one of two forms:

  • Open surgery to fit a synthetic or stent graft
  • Endovascular stent-graft surgery.

Endovascular surgery involves accessing the blood vessels through a small incision near the hip. In stent-graft surgery, an endovascular graft is inserted through this incision using a catheter and is positioned in the aorta to seal off the aneurysm.

In the emergency of a ruptured abdominal aortic aneurysm, the decision over which procedure to perform will be urgent. For elective operations to repair unruptured aneurysms, a review published in 2014 sought to determine the relative risks and benefits of open vs. endovascular surgery.

The review found that while there was a lack of robust studies comparing the two options directly, similar rates of complication were reported for both types of surgery.

The evidence suggested that endovascular aneurysm repair (EVAR) was “less invasive,” but the procedure did “not always significantly alter the postoperative course or length of hospital stay for patients.”

The authors concluded that open surgery still had a role for those patients who were not suitable for endovascular surgery.

Endovascular surgery has become the generally preferred method of aortic aneurysm surgery because of:

  • Shorter operative times
  • Often shorter hospital stays
  • Better levels of surgical experience
  • A perceived lower risk of disease or death surrounding surgery compared with laparoscopic surgery (although the review found this could be more perception than reality).

Endovascular surgery for the repair of aortic aneurysms does carry the following risks however, in addition to the usual risks of surgery:

  • Bleeding around the graft (which requires additional surgery)
  • Bleeding before or after the procedure
  • Blockage of the stent
  • Nerve damage, resulting in weakness, pain or numbness in the leg
  • Kidney failure
  • Reduced blood supply to the legs, kidneys or other organs
  • Erectile dysfunction
  • Unsuccessful surgery that then requires open surgery
  • Slippage of the stent.

Cerebral aneurysm treatment options

Surgical treatment of an aneurysm in the brain is reserved for cases that present a high risk of rupture.

Aneurysms that are less likely to burst are not treated surgically because of the potential risk of brain-damage resulting from possible surgical complications.

In lieu of surgery, patients are given guidance on how to monitor and modify, where possible, the risk factors for rupture of a brain aneurysm. This will likely involve monitoring blood pressure – see prevention below.

Where a ruptured brain aneurysm has led to a subarachnoid hemorrhage (a medical emergency), a patient may be admitted to hospital and undergo brain surgery.

Such a procedure would aim to close off the artery that ruptured due to the aneurysm, in the hope of preventing another bleed.

Prevention of aneurysm

The single most important way a person can reduce their risk of developing an aneurysm is to not smoke or to quit if already smoking. Smoking is not only the strongest risk factor for the development of an aortic aneurysm, it is also one of the greatest risk factors for an aneurysm growing and rupturing.

Smoking is the strongest risk factor for both the development and rupture of aneurysms.

Smoking is a greater risk factor for aneurysm than it is for atherosclerosis, the cardiovascular disease where fatty deposits accumulate on the arterial wall and which can weaken artery walls.

The fact that smoking is also a big risk factor for atherosclerosis is directly relevant, however, because most aneurysms are caused by weakening of the artery wall brought on by atherosclerosis:

Studies have shown that continued smoking induces a significantly faster expansion of aortic aneurysms – by about 0.4 millimeters a year).

Brain aneurysms are not always possible to avoid to the same extent as aortic aneurysms because ruptured brain aneurysms causing subarachnoid hemorrhage stroke can be congenital – present at birth.

Brain aneurysm has both genetic and environmental risk factors, and a history of brain aneurysms in the family is an established risk factor, as is increasing age. However, known risk factors also include, alongside hypertension (high blood pressure), smoking.

Cigarette smoke is also a major source of free radicals which cause oxidative stress. Oxidative stress and resulting tissue damage can occur due to higher production or reduced removal of free radicals. Oxidative stress can also increase inflammation, which contributes to the formation and rupture of cerebral aneurysms.

 

 

TOS : Symptoms, causes and treatments

Thoracic outlet syndrome (TOS) is a condition whereby symptoms are produced (such as numbness in fingers, pain in shoulder, arm, and neck) due to compression of nerves and/or blood vessels in the upper chest. The passageway for these nerves and blood vessels to exit the chest and supply the upper extremities is referred to as the thoracic outlet. Muscle, bone, and other tissues border the thoracic outlet. Any condition that results in enlargement or movement of these tissues of or near the thoracic outlet can cause the thoracic outlet syndrome. These conditions include muscle enlargement (such as fromweight lifting), injuries, an extra rib extending from the neck (cervical rib), weight gain, and rare tumors at the top of the lung. Often no specific cause is detectable.

Thoracic outlet syndrome is a condition whereby symptoms are produced from compression of nerves or blood vessels, or both, because of an inadequate passageway through an area (thoracic outlet) between the base of the neck and the armpit.

Picture of thoracic outlet syndrome (TOS) showing symptom areas

Thoracic outlet syndrome symptoms include

  • neck pain,
  • shoulder pain,
  • arm pain,
  • numbness and tingling of the fingers, and
  • impaired circulation to the extremities (causing discoloration).

What causes thoracic outlet syndroms?

An inadequate passageway for nerves and blood vessels as they pass through an area (thoracic outlet) between the base of the neck and the armpit causes thoracic outlet syndrome. This can be constant or intermittent. Thoracic outlet syndrome can be caused by weight lifting, obesity, tumors in the chest, and extra ribs extending from the seventh cervical vertebra at the base of the neck.

 

What are thoracic outlet syndrome risk factors?

Risk factors include occupations that involve heavy usage of the upper extremities against resistance, including jack-hammer operators and dental hygienists, weight lifting, pregnancy, and obesity. Any condition that causes encroachment of the space for the brachial plexus at the thoracic outlet can lead to thoracic outlet syndrome, including poor posture.

What are thoracic outlet syndrome symptoms and signs?

Symptoms include neck, shoulder, and arm pain, numbness in the fingers, or impaired circulation and flushed sensations to the extremities (causing discoloration). The involved upper extremity can feel weak. Often symptoms are reproduced or worsened when the arm is positioned above the shoulder or extended. Patients can have a wide spectrum of symptoms from mild and intermittent to severe and constant. Pains can extend to the fingers and hands, causing weakness.

What types of doctors treat thoracic outlet syndrome?

Doctors who treat thoracic outlet syndrome include general physicians, such as general-medicine doctors, family medicine doctors, and internists, as well as rheumatologists, physical-medicine doctors, and chest surgeons.

What is the prognosis for thoracic outlet syndrome?

Most people with thoracic outlet syndrome can have complete resolution of symptoms with conservative measures, including exercises specific for thoracic outlet syndrome, physical therapy, and avoiding stressing the tissues of the thoracic outlet. It can be helpful to avoid sleeping with the arms extended above the head. Rarely, surgical intervention can be necessary to take pressure off of involved nerves and blood vessels. Complications include embolization to the hand and nerve damage to the extremity involved.

Is it possible to prevent thoracic outlet syndrome?

It’s possible to prevent thoracic outlet syndrome by maintaining relaxed tissues of the upper chest. This can involve prevention exercises, stretches, and therapies designed to loosen the tissues around the shoulders and neck. 

 

 

 

Endometrial Polyps: Symptoms, Causes & Treatments

Definition

Endometrial polyps or uterine polyps are growths attached to the interior wall of the uterus that expand into the uterine cavity. Excess growth of cells in the endometrium leads to the formation of endometrial polyps. They are by and large noncancerous, though they could turn out to be cancerous in future.

Uterine polyps vary in size from a few millimeters to a number of centimeters. They affix to the uterine wall by a big base or a thin stalk.

A woman can have one or several endometrial polyps. They usually stay enclosed within the uterus, but seldom, they slide down through the gap of the uterus into the vagina. Endometrial polyps generally occur in women who are in the course of or have attained menopause, though younger women can get them too.

Symptoms

Signs of endometrial polyps consist of:

  • Irregular period bleeding
  • Bleeding between the menstrual periods
  • Extreme heavy menstrual periods
  • Vaginal bleeding post menopause
  • Infertility

Risk Factors

Risk factors for developing uterine polyps include:

  • Being perimenopausal or postmenopausal
  • High blood pressure
  • Obesity
  • Intake of tamoxifen, a drug cure for breast cancer

Diagnosis

If the doctor suspects uterine polyps, one of the following will be performed:

  • Transvaginal ultrasound
  • Hysteroscopy
  • Endometrial biopsy

Most endometrial polyps are benign. Nevertheless, some precancerous changes of the uterus or uterine cancers appear as endometrial polyps. The doctor will suggest removal of the polyp and will send a tissue sample for lab examination.

Treatment

For endometrial polyps, the doctor might recommend:

Watchful Waiting: Undersized polyps without signs might resolve on their own. Treatment of small polyps is unnecessary unless there is a risk of uterine cancer.

Medication

Some hormonal medications, including progestins and gonadotropin-releasing hormone agonists, may reduce the symptoms. But taking such medications is usually a short-term solution at best as the symptoms reappear once medication is stopped.

Surgery

Polyps can be removed during hysteroscopy, and sent for histopathological analysis. Depending on the result, further action can be taken.

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