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Support eosinophilic granuloma
Eosinophilic granuloma (EG) is an organization of cells isolated nature of the abnormal differentiation of non-tumor. Eosinophilic granuloma is Langerhan's cell histiocytosis in an expression, previously known as Histiocytosis X. Eosinophilic granuloma occurred in children aged 5-10, violating parts of the bones and lungs. This represents Langerhan's cell histiocytosis 60-80% of cases. Blacks of this disease is extremely rare.
Eosinophilic granuloma can be found in the skull, mandible, spine and long bone. Common in children under 3 years of age, rapidly fatal. Of all Langerhan's cell histiocytosis of 10%. Hand-Schuller-Christian disease (HSC) is a chronic proliferation of Lang's cell histiocytosis rarely form more common in older patients. HSC is the triad of diabetes insipidus, exophthalmos, and skull lesions. Eosinophilic granuloma can be transformed into the systemic disease.
Clinical manifestations of eosinophilic granuloma were: local pain, swelling, ESR increased.
Radiation lesions of eosinophilic granuloma of the performance of non-specific and different parts, the performance difference. Skull skull inside and outside the lesion showed irregular sharp lamellar destruction, a "ramp edge", (Beveled edge), multiple fuzzy boundary defects in the pelvis. Defect occurred in the vertebral spine. Occurred in long bones, is more in the stock dry canal in the metaphysis were. Can cause bone lesions, periosteal reaction. CT scan an


d MRI for the specific scope of intramedullary lesions and the extent of the damage value of cortical bone. Imaging diagnosis with Ewing's sarcoma to be, osteosarcoma, metastatic tumors, and identification of septic osteitis. Reprinted
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[9] picture caption in patients with Sjogren's syndrome - food taboos belongs term pathological Introduction Overof Sjogren's Syndrome Sjogren's syndrome Drying Syndrome can stand alone, but also in other autoimmune diseases, the separate existence of those with primary Sjogren's syndrome, and secondary to rheumatoid arthritis, systemic scleroderma, systemic lupus erythematosus and other autoimmune disease Sjogren's syndrome who is secondary. Sjogren's syndrome is a kind of invasion and exocrine glands, especially the lacrimal and salivary glands characterized by autoimmune disease. Characterized by decreased lacrimal and salivary glands, conjunctivitis, corneal shape and dried with dry mouth. Sjogren's syndrome is a global disease, more than 90% female, age 40-60 years are mostly middle-aged, children less. As far the lack of uniform diagnostic criteria, the prevalence of the disease is very accurate. Generally estimated to be 0.1% - . [enter the term] [see ] image size 300 * 213 px image size 53k image format image / jpeg upload related to entry of admin More contents of the time, anonymous note: Maximum length is 200 characters.


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