Thursday, April 9, 2009

Urticaria pigmentosa

Definition

Urticaria pigmentosa is a skin disease that produces lesions and intense itching. If you rub the lesions, hives may develop.

Alternative Names

Mastocytosis; Mastocytoma

Causes

Urticaria pigmentosa is one of several forms of mastocytosis, which occurs where there are too many inflammatory cells (mast cells) in the skin.

Urticaria pigmentosa is most often seen in children, but it can also occur in adults.



Symptoms

The main symptom is brownish lesions on skin. Rubbing the skin sore causes a hive-like bump. Younger children may develop a fluid-filled blister if it is scratched.

The face may also become flushed.

In severe cases, the following symptoms may occur:

Exams and Tests

  • Skin biopsy to confirm an increase in the number of mast cells
  • Urine histamine

Treatment

Antihistamines may relieve symptoms such as itching and flushing. Discuss the choice of antihistamine with your child's health care provider. Other medications may be recommended for symptoms of more severe and unusual forms of urticaria pigmentosa.

Outlook (Prognosis)

Urticaria pigmentosa goes away by puberty in about half of the affected children. Symptoms usually get better in others as they grow into adulthood.

In adults, urticaria pigmentosa may develop into a more serious condition called systemic mastocytosis.

Possible Complications

Discomfort from itching, and possible self-consciousness about the "spots," are the primary complications. Other problems such as diarrhea and fainting are rare.

Certain medications may trigger flares of urticaria pigmentosa. Discuss these with your doctor.

Bee stings may also cause severe allergic reactions in some patients with urticaria pigmentosa. Your doctor may advise you to carry an injectable epinephrine kit (such as EpiPen or Twinject) to be used in case of a bee sting.

When to Contact a Medical Professional

Call for an appointment with your health care provider if your child has symptoms of urticaria pigmentosa.


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Varicose vein therapy

Definition

Varicose vein therapy is used to treat enlarged veins (varicose veins) that have problems with their valves.

Alternative Names

Vein stripping; Sclerotherapy of veins; Endovenous ablation therapy

Description

Varicose veins usually occur in the legs. Normally, valves in your veins keep blood flowing. But the valves in varicose veins are either damaged or missing. This causes the veins to remain filled with blood, especially when you are standing.



Varicose veins treatments help remove non-moving (stagnant) blood and re-route blood flow through deeper veins in the legs. There are several types of treatment:

  • Surgical vein stripping is an outpatient procedure. You receive general anesthesia, which means you are asleep and do not feel pain. The surgeon makes a cut at the bottom (ankle end) and the top (groin end) of the varicose vein. A thin, plastic, tube-like instrument is placed into the vein and tied around it. When the tube is pulled out, it pulls the vein from out under the skin. Small surgical cuts can also be made over individual veins to remove them.
  • Sclerotherapy is done while the patient is standing. A solution is injected into each varicose vein to cause clotting, which closes off the vein. An elastic bandage is wrapped snugly around the legs after the procedure.
  • Endovenous ablation therapy is an outpatient procedure. The therapy uses heat to destroy vein tissue. A thin catheter (or tube) is inserted into the vein through a tiny skin incision under local anesthesia. Then, using either laser or radiowave (radiofreqency) energy, the vein is heated and cauterized. This closes off the vein.

Today, fewer doctors are performing the traditional vein stripping surgery as more patients choose the less invasive endovenous ablation procedure. The endovenous ablation procedure has shown to work as well as surgery. Patients have significantly less pain and a quicker recovery.

Why the Procedure is Performed

Varicose vein therapy may be recommended for:

  • Varicose veins that cause circulatory problems (venous insufficiency)
  • Leg pain, often described as heavy or tired
  • Skin irritation and sores (ulcers)
  • Blood clots in the veins (phlebitis), which can travel to the lungs (embolism)
  • Cosmetic purposes

Risks

The risks for any anesthesia include:

  • Reactions to medications
  • Problems breathing
The risks for any surgery include:
  • Bleeding
  • Infection
  • Bruising

Unique risks of endovenous varicose vein surgery include:

  • Blood clots (call your doctor if your feet or legs swell)
  • Treated vein opens up
  • Skin burns from heated catheter

Unique risks to sclerotherapy treatment include:

  • Irritation of the vein from the solution
  • Blocked blood flow caused by the solution
  • Leakage of the solution out of the veins into other tissue (can damage surrounding tissue and form ulcers)

Risks associated with any treatment for varicose veins include:

  • Nerve injury
  • Return of the varicose veins

Outlook (Prognosis)

Most patients who undergo varicose vein surgery have good results. Some patients, however, have inflammation and skin discoloration that last for several months following surgery.

Talk to your physician about these risks and your chances for good results.

Recovery

After endovenous ablation therapy and sclerotherapy the patient can almost immediately resume most of their normal activities. Surgical stripping usually requires at least 3 7 days rest, but you could need up to several weeks.

After treatment your legs are wrapped tightly in bandages. Walking is possible the day of surgery. In fact, walking is encouraged to minimize swelling and avoid the risk of deep venous thrombosis, especially with catheter or endovenous treatment.

It is important that feet are kept raised above the heart whenever possible.

References

Rasmussen LH, Bjoern L, Lawaetz M, Blemings A, Lawaetz B, Eklof B. Randomized trial comparing endovenous laser ablation of the great saphenous vein with high ligation and stripping in patients with varicose veins: short-term results. J Vasc Surg. 2007 Aug;46(2):308-15.

Kalteis M, Berger I, Messie-Werndl S, Pistrich R, Schimetta W, Plz W, Hieller F. High ligation combined with stripping and endovenous laser ablation of the great saphenous vein: early results of a randomized controlled study. J Vasc Surg. 2008 Apr;47(4):822-9.

Freischlag JA, Heller JA. Venous disease. In: Townsend CM, Beauchamp RD, Evers BM, Mattox KL, eds. Sabiston Textbook of Surgery. 18th ed. St. Louis, Mo: WB Saunders; 2008:chap 68.

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Leukemia

The leukemia or leukosis is a whole group of tumors which is characterized uncontrolled proliferation and a different degree of a differentiation hematogenic cells. Leukemic cells thus are descendants, clones of one of mutate cells.

The reason of a leukemia, as a rule, are chromosomal aberrations, i.e. variations in structure of chromosomes as a result of various processes of restructuring of their structure: trans location, deletion, inversions, fragmentation.

According to traditional classification, all leukemia share on sharp and chronic. Such division is connected with various capacity of the given tumors to a differentiation proliferating cells. In case of sharp leukosis the differentiation practically is absent, in blood the huge quantity unripe, nonfunctional blast cells that leads to oppression normal hematosis all fragments collects. The specified signs come to light in blood more than in 80 % of cases. Chronic leukosis (leukemia) gives a population of the differentiated cells, is usual granulocytic, one step at a time replacing normal cells of peripheral blood.

Sharp leukemia can be divided on lymphoblastic and myeloblastosis.

* Sharp lymphoblastic leukosis develops from predecessors B-achroacyte (about 75 % cases) more often.
* Sharp myeloblastosis leukosis (the sharp myeloid leukemia) often refers to «nonlymphoid leukemia» to emphasize its variety and difference from Sharp lymphoblastic leukosis since blasts thus can have a granulocytic origin. Sharp 'nonlymphoid leukosis' histological is classified by the letter of M with figures from 0 up to 7, for example, М7 is a sharp megacaryoblast leukemia.

The diagnosis of a leukemia is put on set of researches of blood, and a bone brain. At diagnostics the clinical picture, and cytogenetics, morphology and immunology revealed blasts has not crucial importance. On parameters revealed at it will depend not only statement of the final diagnosis, but also the forecast, treatment and an outcome of disease.

The forecast at leukemia in whole is more favorable at children's age (1-9 years), as well as depends on a type of a pathology, a type of cells and terms of revealing of disease.

The basis of treatment leukosis is made with chemotherapy. Treatment today legal that is why each type of a pathology and its separate features matter for a choice of the report of treatment. At sharp leukosis treatment is based on poly chemotherapy. Its efficiency above at sharp lympholeukosis reaches 95 %. At sharp myeloleukemia efficiency of chemotherapy exceeds 80 %, but reasonably is often accompanied by complications, and 5-years remission is observed only at 40 % of patients, while relapses at Sharp lymphoblastic leukosis – more a unusual occurrence.

As a whole therapy of leukosis should be spent in specialized branch, with an opportunity of application of the most modern and effective treatment that guarantees both a high probability of full remission, and full of recover after all complex of medical actions.

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Amnesia (infringement of memory)

The amnesia - infringement of the memory, shown inability to reproduce earlier the acquired knowledge, the gone through events or to remember the new information.

The passing amnesia can be consequence as diseases, and a craniocereberal trauma. It can extend on events, as preceded a trauma or disease, (a retrograde amnesia), and happened after (an anterograde amnesia).

After a heavy craniocereberal trauma the retrograde amnesia sometimes covers hours and even weeks; memory on more remote events usually does not suffer. In process of recover the period retrograde amnesia is reduced, sometimes down to full restoration of memory. More often, however, patients and cannot recollect event of several last minutes before a trauma. It speaks about infringement of short-term memory, cause of the given events do not send to long-term memory. There are messages on disappearance retrograde amnesia later months or years after a trauma; sometimes restoration is promoted, for example, by hypnosis or narcotherapy. Probably, it is caused by restoration before the broken neural circuits responsible for memory.

Duration of an anterograde amnesia, as a rule, corresponds to duration of posttraumatic infringements of consciousness, however sometimes the anterograde amnesia extends even for that period when short-term memory was already restored also by the patient can to repeat numerical numbers correctly, for example. Duration of anterograde amnesia - a parameter of weight of a craniocereberal trauma. In last turn ability to acquire a new material is restored.

The passing full amnesia is characterized sudden full by an bone-holding amnesia (inability to acquire the new information). Usually it arises at persons older 50 years, is frequent after emotional or physical activity. During an attack of the patient it is not braked, contacted, cognitive functions at first sight are not changed, neurologic symptoms are absent. However it constantly asks that has occured a minute ago, and the impression of confusion of consciousness is often made. During an attack orientation is roughly broken, the patient constantly asks: "Who am I? Where am I? What's with me?" The bone-holding amnesia meshs with an retrograde amnesia on events which have occured directly up to an attack. Memory and other mental functions are restored in some hours, however the patient cannot recollect anything, that occured during an attack.

The reason of disease usually does not manage to be found out. Communication of attacks with cerebrovascular diseases, epilepsy (7 % in one of researches), a migraine, infringements of a rhythm of heart is sometimes traced. At inspection of 277 patients with a passing full amnesia in clinic of Mayo it has appeared, that in the anamnesis 14 % have a migraine and for 11 % - cerebrovascular diseases, however attacks of an amnesia did not coincide with attacks of a migraine or an ischemia of a brain. Approximately at a quarter of patients a passing full amnesia anticipate, but the risk of an insult thus is not raised. Rare cases of sudden and proof loss of memory are described. Approximately at 20 % of patients attacks repeat. The reason happens a migraine, temporal epilepsy, a passing ischemia in pool of a back brain artery.

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Wednesday, April 8, 2009

Adenoma

Adenoma (innocent hyperplasia of prostate gland, to be exact external glands of prostata) - hormonedependent disease at which there is a growth of a tela of prostate gland leading infringement of process urination.

Most often an adenoma diagnose for men older 50 years are more senior, therefore some experts consider the given disease by one of displays of a man's climax. Except for age changes there are some more the factors promoting occurrence of illness:
* hormonal infringements
* presence of other chronic diseases (an atherosclerosis etc.)
* a sedentary way of life
* the big increase in weight of a body
* the ecological factor

At an adenoma under action of testicular hormone (a man's sexual hormone) growth of cells of a ferruterous tela which adjacent direct to a wall of the urethra which are passing through prostate gland begins. Eventually proliferative the tela starts to press on urethra that leads to its narrowing. Than more time there is a disease, especially strong pressure appears on a urethra. Problems with urination begin:
* speeded up urination
* complicated and faltering urination
* a weak pressure of a uric jet
* incontience urine or a sharp delay wet
* erythrocyturia (blood in urine)

As the heaviest cases are considered a sharp delay wet and erythrocyturia. At long-standing current of illness prostate gland increases so, that ejecting a bladder becomes impossible. In such cases of patients urgent hospitalization is required. Occurrence of blood in urine specifies damage of veins of a bladder as a result of elevated pressure in it.
Depending on duration of current of disease and clinical displays allocate three stages of an adenomatosis. At initial stages symptoms of disease are expressed slightly, therefore the patient can not notice them at all. At the first initial stage the patient tests: frequent desires to urination, especially at night-time, time urination increases, a jet wet languid.

At transition of disease to the second stage it is observed: formation of residual urine, difficulty of outflow of urine from a bladder, faltering urination, sensation incomplete ejecting.
The further progress of illness leads to a delay or incontience of urine, internal constrictor loses the tone, can appear nethritic insufficiency.
Quite often the adenoma meshs with other diseases of urinogenital system (a cystitis, an urethritis, a pyelonephritis, urolithic illness, etc.), that is connected with infringement of process urination.
Treatment can be conservative and surgical. Selection of this or that method depends on weight of illness, availability of accompanying diseases, specific features of the patient.

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Tumors of a brain at children

Tumors of the central nervous system win first place on frequency among solid malignant tumours at children, making 20 % of all oncological desease in children's age. These tumors occurs frequency 2-2,8 on 100000 children's population, taking the second place among the reasons of death of children with an oncological pathology. Children of preschool age fall ill more often: the peak of desease is necessary for 2-7 years. Though the parameter lethality from these tumours till now exceeds lethality's parameters at many malignant processes at children, modern therapeutic approaches and advanced achievements in the diagnostic opportunities, allowing early to diagnose a tumour and precisely to plan treatment, allow to cure a lot of children.

Etiology of this group of tumors now it is unknown, though there are data about predisposition of patients for example, with neurofibromatosis, to occurrence at them glioma a brain. Communication of occurrence neurogliocytoma at children with a syndrome basocellular nevus (defeat of a skin, anomaly of a skeleton, a leather, brushes, feet and anomalies of central nervous system) is known. The raised desease of tumors of a brain is marked at children with a congenital immunodeficiency, at children with ataxia-venous lake.

Often tumor of a brain arises as the second tumor at children, suffering sharp leukosis, a hepatocellular cancer, adrenocortical tumors. All these data attest to availability of some contributory causes for progress of malignant tumours of a brain, to decipher which and to define their influence on the forecast it is necessary in the future.

Classification of tumors of a brain at children.

According to the international classification the CART (1990, the second edition) biological behaviour of tumours central nervous system it is defined (in addition to presence of histologic features of a differentiation) so-called, a degree malignity or anaplasia: from I (good-quality) up to IV (malignant). To tumors low degrees of malignity belong to tumor I-II of a degree (Low grade), to a high degree of malignity
- III-IV degrees (High grade).

The histologic structure of tumours of a brain at children significantly differs from those at adults. Meningiomas, neurilemmomas, tumors of a hypophysis and metastasises from other bodies which rather often amaze brain of adult patients, very seldom meet at children's age. At children of 70 % of tumours make gliomas.

The first classification of tumors of a brain has been offered in 20th years of our century Bailey and Cushing. This classification is based on histogenesis fabrics of a brain and the subsequent classifications have all in to the basis this principle.

The tumors of a brain diagnosed for children of the first years of a life, have the central arrangement, i.e. amaze more often the third ventricle, hypothalamus, chiasm optic nerves, an average brain, the bridge, a cerebellum and the fourth ventricle. In spite of the fact that the volume of substance of a brain of a back cranial pole makes only the tenth part from all volume of a brain, more than half of all malignant tumors of a brain at children is more senior than 1 year make tumors of a back cranial pole. It mainly - neurogliocytoma, cerebellar astrocytoma, gliomas of a trunk of a brain and ependymoma the fourth ventricle,.

Clinical picture.

Generally speaking, any tumor of a brain has malignant behaviour irrespective of it the histologic nature as its growth occurs in the limited volume, and irrespective of the histologic nature of a tumour the clinical picture of all tumours of a brain is defined, mainly, localization of tumoral growth, age and a preclinical level of development of the sick child.

Central nervous system neoplasms can cause neurologic frustration by direct infiltration or prelum normal structures, or mediated, causing of obstruction neurolymph ways.

The factor defining dominating symptoms at children by tumours of a brain, the raised intracranial pressure is, in consequence of that there is a classical triad - a morning headache, vomiting and drowsiness. Heavy, anticipate the headache seldom arises at children, but it is especially important to pay attention to this complaint. Spasmes - the second symptom on frequency after a headache, especially at children with suprasternal tumors. Approximately at a quarter of such patients of a spasm are the first demonstration of a tumour. Sometimes these children aspire to incline a head in one party. Involving in process of a cerebellum can cause ataxia, nystagmus and others cerebellar frustration.

Diagnostic.

Besides routine clinical inspections, including survey of the oculist, to such children should be necessarily lead CT and MRT with contrast substance head and a spinal cord. Especially at localization of a tumor in back to pole MRT it is extremely informative, as this method has greater resolution. These researches with success have replaced intrusive procedures - arterial angiography or air ventriculography.

Histologic verification of a tumor is necessary, but is at times complicated because of the technical difficulties connected with localization of a tumour, involving in process the vitally-important structures. Now with gradual ocurrence in practice of neurosurgeons of a new hi-tech method of operative intervention - stereotactic surgeries begins possible to make biopsy tumors practically any localization. Sometimes in communication with substantial growth of intracranial pressure by a first step operation of shunting is, that considerably improves the neurologic status of the patient.

Cerebrospinal research will give a-brain liquid the information about possible extracratonal distribution of malignant process. In rare cases of distribution of a tumor for central nervous system limits (for example, at presence neurogliocytoma) carrying out of additional diagnostic actions, such as x-ray of a thorax, ultrasonic of a belly cavity, myelogram is necessary.

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Keratoconus

Definition

Keratoconus is a deterioration of the structure of the cornea with gradual bulging from the normal round shape to a cone shape.

Causes

The cause is unknown. Keratoconus is more common in contact lens wearers and people with nearsighted eyes. Some researchers believe that allergy may play a role.

Symptoms

This condition causes decreased visual acuity. The earliest symptom is subtle blurring of vision that cannot be corrected with glasses. (Vision can generally be corrected to 20/20 with gas-permeable contact lenses.)

Exams and Tests

Keratoconus is frequently discovered during adolescence. It can usually be diagnosed with slit-lamp examination of the cornea. Early cases may require a test called corneal topography, which creates a map of the curvature of the cornea.

When keratoconus is advanced, the cornea may be thinner in areas. This can be measured with a painless test called pachymetry.



Treatment

Contact lenses are the primary treatment and are satisfactory treatment for most patients with keratoconus. Severe cases may require corneal transplantation.

Newer technologies may use high frequency radio energy. This energy shrinks the edges of the cornea, which pulls the central area back to a more normal shape. It can help delay or avoid the need for a corneal transplantation.

Outlook (Prognosis)

In most cases vision can be corrected with gas-permeable contact lenses. Where corneal transplantation is needed, results are usually good after a long recovery period.

Possible Complications

Patients with keratoconus should not have laser vision correction. Corneal topography is usually done before laser vision correction to rule out people with this condition.

When to Contact a Medical Professional

Young persons whose vision cannot be corrected to 20/20 with glasses should be evaluated by an eye doctor experienced with keratoconus.

Prevention

There are no preventive measures. Some specialists believe that patients with keratoconus should have aggressive treatment of ocular allergy and should be instructed not to rub their eyes.

References

Kymionis GD, Siganos CS, Tsiklis NS, et al. Long-term follow-up of Intacs in keratoconus. Am J Ophthalmol. Feb 2007;143(2):236-244.

Fay A. Diseases of the visual system. In: Goldman L, Ausiello D, eds. Cecil Medicine. 23rd ed. Philadelphia, Pa: Saunders Elsevier; 2007:chap 449


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