Thursday, March 19, 2009

Bunions

Definition

A bunion is when your big toe points toward the second toe. This causes a bump on the edge of your foot, at the joint of your big toe.

Alternative Names

Hallux valgus

Causes

Bunions occur more commonly in women and sometimes run in families. People born with abnormal bones in their feet are more likely to form a bunion. Wearing narrow-toed, high-heeled shoes may lead to a bunion. The condition may become painful as extra bone and a fluid-filled sac grow at the base of the big toe.



Symptoms

  • Red, calloused skin along the foot at the base of the big toe
  • A bony bump at this site
  • Pain over the joint, aggravated by pressure from shoes
  • Big toe turned toward the other toes

Exams and Tests

A doctor can usually diagnose a bunion by looking at it. A foot x-ray can show an abnormal angle between the big toe and the foot and, in some cases, arthritis.

Treatment

When a bunion first begins to develop, take good care of your feet and wear wide-toed shoes. This often solves the problem and prevents the need for any further treatment. It may help to wear felt or foam pads on the foot to protect the bunion, or devices to separate the first and second toes at night. These are available at drugstores. You can also try cutting a hole in a pair of old, comfortable shoes to wear around the house.

If the bunion gets worse -- resulting in severe deformity or pain -- surgery to realign the toe and remove the bony bump (bunionectomy) can be effective. There are over 100 different surgical techniques that have been described to treat this condition.

Outlook (Prognosis)

The outlook depends on your age and activities, and the severity of the bunion. Teenagers may have more trouble treating a bunion than adults. Many adults do well by caring for the bunion when it first starts to develop, and wearing different shoes. Surgery reduces the pain in many, but not all, people with bunions.

Possible Complications

  • Chronic foot pain
  • Foot deformity
  • Stiff foot
  • Hallux varus (occurs with surgical over-correction, where the toe points away from the second toe)

When to Contact a Medical Professional

Call for an appointment with your doctor if the bunion:

  • Continues to cause pain even after self care, such as wearing wide-toed shoes
  • Prevents you from doing your usual activities
  • Has any signs of infection (like redness or swelling), especially if you have diabetes

Prevention

Avoid compressing the toes of your foot with narrow, poor-fitting shoes.

References

Vanore JV. Diagnosis and treatment of first metatarsophalangeal joint disorders. Section 1: Hallux valgus. J Foot Ankle Surg. 2003; 42(3): 112-123.

King DM. Associated deformities and hypermobility in hallux valgus: an investigation with weightbearing radiographs. Foot Ankle Int. 2004; 25(4): 251-255.

Ferrari J, Higgins JP, Prior TD. Interventions for treating hallux valgus (abductovalgus) and bunions. Cochrane Database Syst Rev. 2004.


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Donovanosis. Venereal granuloma

Except for the name «donovanosis» this venereal illness also refers to venereal granuloma, the fifth venereal illness, is simple granuloma or granulomatosis, tropical inguinal granuloma, granuloma ulcer genitals, inguinal granuloma. The name «granuloma» occurs from a latin word granulum – "kernel", and there was it of that the basic symptoms of venereal granuloma are really reminding grains papule – small pimples on genitals.

Speaking about classical venereal diseases, venereologists, as a rule, keep in mind five diseases. Two of them – a syphilis and a gonorrhoea – are widely widespread worldwide. Other three concern to type of rare infections in Russia, transferred by sexual contact. It is soft chancre («the third venereal illness»), inguinal megakaryoblastoma («the fourth venereal illness»), and, finally, venereal granuloma («the fifth venereal illness»).

In comparison with "counterparts", especially with a syphilis, donovanosis looks a harmless sore. However harmless venereal illnesses does not happen, and venereal granuloma is not exception. Complications granulomatosis if they are reached with business, can be more than serious and dangerous to human life.

Venereal granuloma is the chronic infection transferred, similarly to other venereal illnesses, first of all sexual by and slowly progressing in an organism of the infected person. Adults are ill venereal granuloma only, it is not transferred children.

The activator of venereal granuloma (donovanosis) owing to which illness has received this name, – bodies Donovan which refers to also Calymmatobacterium granulomatis or stick Aragan-Vianne. It is fine (1-2 microns) a bacterium bean-like or ovoid forms. At contact to patients, bacteria take root into a leather of genitals, perineum and other sites, causing disease.

In Russia cases venereal granuloma – a huge rarity as this illness is specific to the tropical countries with a warm and damp climate. Especially widely venereal granuloma it is widespread in Papua-new Guinea, Southern India, Southern Africa, the countries of Caribbean basin, in separate areas of Australia and Brazil. In America and in the Europe "brought in" cases venereal granuloma are registered only. There are scattered instances venereal granuloma and in Russia. Among our compatriots basically the people going in tropics on rest and interested persons to try of local "exotic" including in intimate relations catch.

Certainly, sick venereal granuloma the person can transfer an infection to the constant partner, but such cases – an even greater rarity, as venereal granuloma, on medical terminology, «rather less contagious». It means, that in difference, we shall tell from a gonorrhoea who is almost always transferred the healthy partner from the patient at the first not protected contact, venereal granuloma at sexual contact is transferred seldom enough.

According to statistics, the risk to catch venereal granuloma at the unitary not protected sexual contact to patients can change from 1 up to 50 %. Thus it is necessary to consider, that the damp climate and enough heat of an environment is necessary to a bacterium. Hence, arrived of tropics to Russia infected venereal granuloma "holidayer" is practically safe for constant partners, both at sexual attitudes, and at household contacts. And still it is better to not risk, because even 1 % of probable infection for one person can be quite enough.

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Tuesday, March 17, 2009

Cervical Cancer

Description

An in-depth report on the causes, diagnosis, treatment, and prevention of cervical cancer.

Alternative Names

Dysplasia; Human Papillomas Virus; Pap Smear

Treatment for Invasive Cervical Cancer

Radiation therapy and surgery are about equally effective as a single option for treating very small cervical cancers in their earliest stages, with survival rates of up to 85% to 90% in appropriate patients. Factors influencing the choice between radiation therapy and surgery in women with invasive cancer include the patient's age and health and the extent of the disease. Both surgery and radiation therapy eliminate the possibility of having children in premenopausal women.

Although treatments for cervical cancer have several potentially severe side effects, they are usually well-tolerated. Women undergoing any of these treatments should feel free to seek support groups and counseling, which can be as important for their outlook as medical therapies.



Surgery

In the early stages of cervical cancer, surgery is often the preferred primary treatment approach since it preserves normal sexual function. Surgery for invasive cancer is nearly always hysterectomy. Some patients desiring fertility who have early stage I cancer may be candidates for cervical cone biopsy.

Hysterectomy. A hysterectomy attempts to eliminate the cancerous tissue by removing the uterus. There are several variations of this operation, depending on the location of the tumor. In women of childbearing age, the ovaries can usually be left intact. Although a woman who has a hysterectomy but retains her ovaries cannot bear children, she will not go into premature menopause. (Studies indicate that leaving the ovaries intact is safe for most women and does not pose any greater risk for cervical cancer recurrence.)

A simple hysterectomy involves the removal of the uterus and the cervix, but leaves the parametrium (tissue surrounding the uterus) and vagina intact. Lymph nodes in the pelvis are not usually removed.

Hysterectomy - series Click the icon to see an illustrated series detailing a hysterectomy.

A radical hysterectomy removes not only the uterus and the cervix but also the parametrium, the supporting ligaments, the upper vagina, and some or all of the local lymph nodes (a procedure called lymphadenectomy).

If the cancerous tumor recurs within the pelvis after primary treatment, a more extreme procedure may be performed called a pelvic exenteration, which combines radical hysterectomy with removal of the bladder and rectum. (In such cases, plastic surgery may be needed afterward to recreate an artificial vagina.) Patients undergoing this procedure are physically and psychologically screened in advance to determine whether it is an appropriate choice. The success rate for pelvic exenteration in halting the progression of the disease is approximately 25% to 45%.

Any form of hysterectomy is major surgery and requires at least a three to five day hospital stay. Although hysterectomy typically uses a wide abdominal incision, less invasive techniques that allow shorter recovery time may be possible for some women with early stage cancers if performed by experienced surgeons.

Side effects include difficulty emptying the bladder or bowels and a painful lower abdomen. Urinary tract infections are very common. Complications include fistulas (abnormal channels within the pelvis, which in this case are a result of surgery), bladder dysfunction, and cysts.

Normal activity, including intercourse, can be resumed in about four to eight weeks. Once the uterus is removed, menstruation will cease. If the ovaries are removed, the symptoms of menopause will begin. These symptoms are likely to be more severe in surgical menopause than in the course of a natural passage to menopause. Hormone replacement therapy should be considered. [For more information on hysterectomy see the Well-Connected Report #73, Fibroids: Uterineor Report #74, Endometriosis.]

Trachelectomy.An experimental procedure called trachelectomy is being investigated for preserving fertility in certain women in early stage cancer, but it is highly controversial and appropriate in only about 5% of cervical cancer patients. In the procedure, only the cancerous portion of the cervix is removed, while the uterus and the rest of the cervix are left intact. The cervix is closed with a suture.

Small, early studies suggest it may be effective for early stage 1 patients with no risk factors for aggressive cancer. In two small 1999 and 2000 studies, conception rates were between 27% and 37%, and survival rates after two years were over 95%. The procedure is primarily performed outside the US, and few American surgeons are skilled in this surgery at this time. Throughout the world, in fact, only about a few hundred of these procedures have been performed to date. Women should also realize that conception rates are still lower than normal. And even if they can get pregnant, there is a very high risk for miscarriage because the cervix is weakened. Larger and longer-term studies are needed to confirm its long-term safety.

Radiation

Radiation therapy is an alternative approach for early stage cervical cancer. Radiation with concurrent with cisplatin-based chemotherapy is now the standard treatment for locally advanced cervical cancer. Radiation therapy employs high-energy rays aimed at the body from an outside machine (external beam radiation) and radioactive materials placed inside the body against the cervix (intracavitary radiation).

  • External beam radiation is given first and aimed at the lymph nodes along the pelvic wall. It usually involves a short period of direct-radiation five days a week for about six weeks in an outpatient setting.
  • Intracavitary radiation (also called brachytherapy) follows and is designed to deliver high doses of radiation to the local tumor area. Radioactive material, typically cesium-137, is encapsulated in both gold and platinum. These capsules are inserted in a long stainless steel tube, called a tandem, which is inserted in the uterus and in small stainless steel cylinders, called colpostats, which are placed against the cervix as close to the cancerous cells as possible. Commonly, two or more radiation treatments are administered for about 35 hours each time. Radiation implants may also be inserted directly into the tumor using a needle.

In order to be effective, radiation therapy must be powerful enough to destroy the cancer cells' capacity to grow and divide. This means that normal cells are also affected, which may cause significant side effects. Fortunately, healthy cells usually recover quickly from the damage, whereas abnormal cells do not.

Advanced methods for targeting radiation more precisely are now available that limit the damage to healthy tissue. They include 3-D conformal radiation and intensity-modulated radiation therapy (IMRT):

  • 3-D conformal techniques use computers and a three-dimensional image of the cervix to provide precise targeting of the tumor using multiple high-dose radiation beams.
  • IMRT also uses 3-D techniques and employs very thin and precise beam at various intensities.

Side Effects. Side effects of radiation therapy include fatigue, redness or dryness in the treated area, diarrhea, frequent or uncomfortable urination, and vaginal dryness, itching, or burning. After treatment, side effects usually disappear.

Long-Term Complications. Complications include proctitis (inflammation of the rectum) and cystitis (inflammation of the bladder). Bowel obstruction is an uncommon complication. Radiation therapy may also cause vaginal scarring, sexual difficulties, and premature menopause in younger women. Occasionally an abnormal tunnel between the bladder and the vagina, known as a vesicovaginal fistula, will develop and may require surgery.

Click the icon to see an image of the female anatomy.

Investigative temporary silicone implants or a noninvasive device called the belly board may protect the small intestine during radiation therapy and help reduce complications.

Radiation itself may increase the risk for later development of cancer in the area surrounding the treated tissue. Although newer more precise radiotherapy approaches should reduce this risk, there is some concern that IMRT may double the incidence of secondary cancers over time compared to 3-D conformal techniques. This is of particular concern in younger patients.

Radiation and Hyperthermia. Investigators are studying hyperthermia (use of high heat often provided by ultrasound) in combinations with radiation therapy. This approach has shown some promise in achieving significant response rates in small studies. Comparison studies are important to determine if this approach would be as beneficial with radiation therapy as concurrent chemotherapy.

Chemotherapy

Chemotherapy employs cell-killing drugs, known as cytotoxic agents, to destroy widespread cancer cells that have spread from their point of origin (the primary tumor) and are, therefore, no longer treatable by surgery or radiation.

For many years, chemotherapy was only used with very advanced disease to reduce symptoms. Platinum-based chemotherapy agents (usually cisplatin) are now being used in many situations for cervical cancer including the following:

  • In combination with radiation therapy to improve survival rates in certain women, including some with locally advanced cancer.
  • In some women with locally advanced cancer to reduce tumors to the point where the cancer may be operable.
  • When cancer has spread (metastasized), mostly to reduce symptoms such as pain.

Chemotherapy Agents Used.

  • Platinum-Based Agents. One of the most active chemotherapeutic agents for cervical cancer is cisplatin, which enhances the effectiveness of radiation in the treatment of patients with more advanced disease stages. Cisplatin and carboplatin are known as platinum-based drugs. In general, platinum-based agents are the standard drugs used for this disease. Concurrent platinum-based agents and radiotherapy are important treatments for many later cancer stages. Even in treating metastatic disease, cisplatin used alone has been more helpful than even combinations of agents. There is some evidence that a combination of platinum plus paclitaxel with possibly other single agents may be more effective than platinum alone in the treatment of metastatic disease. Other platinum agents, such as nedaplatin, are under investigation.
  • Drugs that Enhance Radiation. Some drugs being investigated appear to increase tumor response to radiation therapy, and so are known as radiation sensitizers or enhancers. Topotecan, a radioenhancer, for example, is showing some promise in early studies, although toxicity is high.
  • Other Agents. Other drugs, mostly used in combinations, have also been investigated with some promise. They include with epirubicin, irinotecan, paclitaxel, bleomycin, mitomycin, vinorelbine, gemcitabine, and doxifluridine.

For cancer that has spread to other areas from its original source (metastatic disease), chemotherapy regimens may use single cytotoxic agents or several agents in combination.

Administration. Cytotoxic agents may be given orally or as injections. Treatment may be administered at a medical center, physician's office, or even a patient's home. Some patients receiving chemotherapy may need to remain in the hospital for several days so the effects of the drugs can be monitored. The drugs are often administered in cycles with a period of rest following a period of treatment in order to allow a recovery from the side effects.

Side Effects. Chemotherapy affects all fast-growing cells, including healthy ones, so some side effects are inevitable. Side effects occur with all chemotherapeutic drugs. They are more severe with higher doses and increase over the course of treatment.

Common side effects include the following:

  • Nausea and vomiting. Drugs known as serotonin antagonists, especially ondansetron (Zofran), can relieve these side effects in nearly all patients given moderate drugs and most patients who take more powerful drugs. In one study, a combination of dexamethasone (a corticosteroid) with ondansetron taken within 24 hours of chemotherapy achieved either a major or complete reduction in nausea and vomiting.
  • Diarrhea.
  • Temporary hair loss.
  • Weight loss.
  • Fatigue.
  • Anemia.
  • Depression.

Complications. Serious short- and long-term complications can also occur and may vary depending on the specific agents used. They include the following:

  • Increased chance for infection from suppression of the immune system.
  • Severe drops in white blood cells (neutropenia). Certain agents, such as taxanes, pose a higher risk for this than other chemotherapeutic drugs. White blood cell count may be improved with the addition of a drug called granulocyte colony-stimulating factor (either filgrastim and lenograstim).
  • Liver and kidney damage.
  • Abnormal blood clotting (thrombocytopenia).
  • Allergic reaction, particularly to platinum-based agents. (A simple skin test in under investigation that may identify people with a potential allergic response.).
  • Menstrual abnormalities are common and premature menopause occurs in about 30% of women, particularly in those over 40.
  • Rarely, secondary cancers such as leukemia.
  • Between a quarter and a third of women report problems in concentration, motor function, and memory, which may be long-term. This effect may be due to reductions in estrogen levels after treatments.

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Spasticity

Definition

Spasticity is stiff or rigid muscles with exaggerated, deep tendon reflexes (for example, a knee-jerk reflex). The condition can interfere with walking, movement, or speech.

See also: Muscle cramps

Alternative Names

Muscle stiffness

Considerations

Spasticity generally results from damage to the part of the brain that controls voluntary movement. It may also occur when you have damage to the nerves traveling from brain down to spinal cord.

Symptoms of spasticity include:

  • Exaggerated deep tendon reflexes (the knee-jerk reflex)
  • Scissoring (crossing of the legs as the tips of scissors would close)
  • Repetitive jerky motions (clonus)
  • Unusual posturing
  • Carrying the shoulder, arm, wrist, and finger at an abnormal angle

Spasticity may also interfere with speech. Severe, long-term spasticity may lead to contracture of muscles, causing joints to be bent at a fixed position.


Causes

This list is not all inclusive.

Home Care

Exercise, including muscle stretching, can help make your symptoms less severe.

When to Contact a Medical Professional

Contact your health care provider if:
  • The spasticity worsens
  • Contracture deformities appear to be developing
  • Your condition gets worse

What to Expect at Your Office Visit

Your doctor will perform a physical exam and ask questions about your symptoms, including:

  • When was it first noticed?
  • How long has it lasted?
  • Is it always present?
  • How severe is it?
  • What muscles are affected?
  • What makes it better?
  • What makes it worse?
  • What other symptoms are also present?

Your doctor may refer you to a physical therapist. Physical therapy consists of variety of exercises, including muscle stretching and strengthening exercises. Physical therapy exercises can be taught to parents who may then help their child perform them at home.

Medicines for spasticity include baclofen, tizanidine, cyclobenzaprine, and benzodiazepines. In rare cases, a pump may be inserted into the spinal fluid to directly deliver medicine to the nervous system.

Botox injections may help relieve spasticity symptoms in some patients.

Sometimes, a person may need surgery to release the tendon or to cut the the nerve-muscle pathway.

References

Goetz, CG. Textbook of Clinical Neurology. 2nd ed. St. Louis, Mo: WB Saunders; 2003: 236, 247, 254.

Goldman L, Ausiello D. Cecil Textbook of Medicine. 22nd ed. Philadelphia, Pa: WB Saunders; 2004:2324.


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Multiple Endocrine Neoplasia

- Diverse endocrine and metabolic infringements
- Symptoms are caused by infringements of secretion of one or several hormones
- Tumors often happen malignant
- The majority of tumors has a neuroectodermal origin
- Quite often syndromes of multiple endocrine neoplasia are accompanied of dysplasia of other organs and telas
- Both sporadic and family cases of multiple endocrine neoplasia are caused by genetic defects and inherited autosomal-dominant

The historical information:

- Communication between plural endocrine infringements and plural tumors of endocrine glands has been noticed by pathologists in the end of the last century. However modern representations about syndromes of multiple endocrine neoplasia have started to be formed in 50th years XX of a century. First Wermer has found out in several patients a combination of a hyperplasia of epithelial body, tumors of a hypophysis and tumors from insular cells and has suggested to name this syndrome plural endocrine adenomatosis (the modern name - multiple endocrine neoplasia type 1). A little bit later J. H. Sipple has described a syndrome including a medullar cancer of a thyroid gland and chromaffinoma. Today this syndrome can be named multiple endocrine neoplasia type 2a. Then R. N. Schimke has allocated a version of this syndrome, shown plural neuroma and other hereditary infringements (multiple endocrine neoplasia type 2b).

- Some hereditary syndromes, traditionally considered independent diseases, can be components of syndromes of multiple endocrine neoplasia. For example, the some endocrinologists consider Zollinger-Ellison syndrome as a component of multiple endocrine neoplasia type 1.

Genetics:

- All syndromes of multiple endocrine neoplasia are inherited autosomal-dominant and are characterized with high penetrance. In half of cases multiple endocrine neoplasia arises sporadically, i.e. is caused by again appeared mutation in sexual or somatic cells. The risk of disease at the child of the patient with sporadic multiple endocrine neoplasia makes 50 %. In families with multiple endocrine neoplasia the risk exceeds 75 %. Genealogic, cytogenetic and molecular-genetic researches have revealed the mutations underlying known types multiple endocrine neoplasia. These mutations can be found out by ПЦР with the subsequent hybridization about a site-specific oligonucleotides and to calculate individual and family risk of multiple endocrine neoplasia.

- Hypotheses. Tumors, characteristic for syndromes of multiple endocrine neoplasia, occur from cells of system APUD. According to the theory Pearse (1966), all cells of system APUD are derivatives of cells neuroectoderm (a nervous crest). Assume, that syndromes of multiple endocrine neoplasia are caused by mutations in cells of a nervous crest. These mutations are inherited by cells of endocrine glands and other cells of system APUD and lead to their tumoral transformation. In favour of this hypothesis existence of the so-called mixed types МЭН including hyperplasia of single cells of system APUD or tumours from such cells testifies. To mixed types of multiple endocrine neoplasia carry, for example, neurofibromatosis with attributes of multiple endocrine neoplasia types 1, 2а and 2b.

Against this hypothesis shows that fact, that at syndromes of multiple endocrine neoplasia quite often there are the new growths having an endodermal or a mesenchymal origin. It is not excluded, that the mutation causes transformation of cells only in one endocrine gland, and accompanying infringements have secondary character and are caused by hypersecretion of a hormone by cells of a primary tumour. It is known, for example, that at of multiple endocrine neoplasia type 1 hypersecretion of insulin by cells insulinoma causes hyperplasia of adenohypophysis.

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Sunday, March 15, 2009

Etiology of Bacterial meningitis

The main activators of a bacterial meningitis is Haemophilus influenzae, Neisseria meningitidis and Streptococcus pneumoniae. All over the world they cause 75-80 % of cases of this disease, though a parity between these three activators in the different countries variously.

The meningitis caused Haemophilus influenzae, meets almost exclusively at children till 6 years. More than 90 % of Haemophilus influenzae's stock concern to type B; all of them encapsulated. To a meningitis precedes carrier state of microorganisms in a nasopharynx with their subsequent penetration into a blood-groove.

Neisseria meningitidis (meningococcus) usually causes a meningitis in children and young men. Epidemics usually caused by microorganisms are possible in serogroups A and B, less often in others serogroups. Neisseria meningitidis of serogroup B cause the majority of sporadic cases of a meningococcal meningitis. About 50 % of cases of a meningitis in the USA are caused by activators of this serogroup. Recently frequency of the infections caused Neisseria meningitidis serogroup B increases in Northern America, - first of all stocks which concern to clone ЕТ-15. These stocks cause flashes of disease with high fatality rate is more often. Stocks of serogroup Y cause a pneumonia. About 20 % of bacterial meningitises in the USA - meningococcal. One of the reasons of disease can be carrier state Neisseria meningitidis in a nasopharynx. The contributing factor - insufficiency of components of complement С5, С6, С7, С8 and, probably, С9 (membrane attack complex); thus the risk of the infections caused Neisseria spp., increases in 8000 times, however fatality rate decreases.

Activators of a bacterial meningitis at people 30 years are more senior more often happens Streptococcus pneumoniae (pneumococcus). In the age of 60 years a pneumococcus meningitis are more senior meets much more often, than at children. Streptococcus pneumoniae causes about 15 % of cases of a bacterial meningitis in the USA. At extramural contamination (from 1962 to 1988) has shown the analysis of 262 cases of a meningitis, that the most frequent activators were Streptococcus pneumoniae (37 %), Neisseria meningitidis (13 %) and Listeria monocytogenes (10 %). Ftality rate at a pneumococcus meningitis at adults remains high - 19-30 %.

The pneumococcus meningitis is usually complication of a pneumonia, an average otitis, mastoid disease, a sinusitis or infectious endocarditis. Contributing factors heavy pneumococcus infections - splenectomy, congenital asplenia or functional asplenism, erythroid myeloma, hypogammaglobulinemia, an alcoholism, a cirrhosis of a liver and Wiscott-Aldrich syndrome. Streptococcus pneumoniae - the most frequent activator of a meningism at crises of the basis of the skull, complicated by liquorrhea.

The meningitis caused Listeria monocytogenes, seldom meets in the USA, however fatality rate at it there is high. These microorganisms amaze newborns/elderly, the people, suffering with an alcoholism, a diabetes, malignant new growths, as well as adult population with the weakened immunity (for example, after transplantation of a kidney or at AIDS) is more often.

Encephalomeningitis, caused by Listeria monocytogenes, after transplantation of a kidney it is possible to reduce desease by means of preventive purpose trimethoprim/sulfamethoxazole. About in 30 % of cases circling disease at adults and in 50 % - at children do not find any contributing factors. Flashes of heavy circling disease are possible at the use in food of the infected milk, cheese or salad from crude cabbage, carrots and an onions.

The meningitis caused aerobic by gram-negative sticks, meets seldom. Exception newborns and make older people. So, at newborns the activator of a bacterial meningitis in 30-50 % of cases happens Escherichia coli. The meningitis after a craniocereberal trauma and neurosurgerical interventions, at older people, at an immunodeficiency, strongyloidosis or bacillemia can be caused Klebsiella spp., Escherichia coli and Pseudomonas aeruginosa. Prevalence of the meningitis caused by gram-negative sticks, is rather insignificant, but death rate remains high. Gram-negative sticks often happen activators of hospital infections, however frequency of the meningitis caused by these microorganisms at extramural contamination, recently increases - especially among the older people weakened, suffering an alcoholism and a diabetes.

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What can be a result of hepatitis?

Infection with a virus of a hepatitis, most probably leads to development of a hepatitis.

After infection there comes the incubatory period - time from penetration of a virus into blood before the first signs of disease (so - and developments of the certain changes in a liver). At a hepatitis A, B, C this period can be from 10-20 to 100-200 days and it depends on many factors. Development of a hepatitis passes a sharp phase - the first displays of an infection which can be appreciable and even heavy.

Then the recover could happens, when the virus leaves an organism and the condition of a liver comes to norm. Recover comes after all cases of a sharp hepatitis A and in most cases a of hepatitis B.If it will not occur, the chronic hepatitis develops.
The reasons on which there does not come recover after a sharp infection, usually carry to a condition of immune system. Unequivocally to tell, at whom there will come recover and at whom - is not present, it is impossible.

The chronic hepatitis develops at 5-10 % infected by a virus of a hepatitis B and at, at least, 60 % infected by a virus of a hepatitis C.

How the hepatitis can long proceed?

Sharp hepatitis usually come to the end with recover within 6 months. If the hepatitis proceeds longer than 6 months, speak about a chronic infection. Chronic hepatitis C and B have long-standing, long-term current. Even if thus long time is not observed displays of a hepatitis, the virus can be kept in a liver and continues. The risk of dangerous consequences of all this time is kept. At absence of displays of a hepatitis, but a constant tracking down of signs of a virus (markers of a virus hepatitis) speak about the chronic carrier. The carrier of a virus can become the reason of infection of other people. However carrying does not mean safety for the carrier.

What most dangerous consequences of a hepatitis?

The most dangerous consequence of a sharp hepatitis - development heavy fulminant forms of disease. It occurs seldom: nearby 1 % of cases of a hepatitis A and B in fulminant forms. The most dangerous consequences of a chronic hepatitis - development of a cirrhosis of a liver and a cancer (hepatocellular carcinoma). It occurs on a regular basis. The cirrhosis of a liver develops in 20% of cases of a chronic hepatitis B and in 5-20% of cases of hepatitis C. Virus hepatitis may cause the majority of cases of a cancer of a liver and serve as a principal cause of its change.

Whether can bring a hepatitis to ruin ill?
When it occurs?

The risk of a lethal outcome at sharp forms of a virus hepatitis is insignificant. It fulminant forms of a hepatitis B, as well as 0,1-2,1 % of cases of a hepatitis A with greater probability at adults. The risk of destruction from consequences of a chronic hepatitis makes 15-50 %. At development of a cirrhosis of a liver up to 50 % sick of a chronic hepatitis B and C perishes within 5 years. Outcomes of a chronic hepatitis In are included into number 10 of principal causes of death at men in developing countries (data the CART).

What hepatitis are more dangerous?

All a virus hepatitis are dangerous in their own way, one during the sharp period, others in connection with chronic current and risk of development of a cirrhosis of a liver.
No hepatitis can be disregarded.

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