Histiocytosis, also referred to as Langerhans Cell Histiocytosis (LCH), and formally called Histiocytosis X, represents a group of rare disorders involving specific cells that normally have important roles as part of the immune system. While the cause of LCH is unknown, LCH can frequently behave like cancer and so is … See more The exact cause of histiocytosis is unknown. However, recent studies indicate that it is caused by the development and expansion of an … See more Diagnostic tests include: a biopsy, in which a small sample of skin and/or bone is taken and examined under a microscope for abnormal cells; routine and sometimes specialized X-rays and … See more The first sign of histiocytosis is often a rash on the scalp, similar to cradle cap. There may be a pain in a bone, discharge from the ear, loss of appetite and fever. Sometimes the stomach is swollen and painful. … See more Depending on the extent of the disease, LCH is often treated with chemotherapy and steroids to suppress the function of the immune system … See more WebBrain involvement with ECD often shows a subtle parenchymal infiltrate by single histiocytes with nonlipidized cytoplasm, 18 and in other cases presents with mass lesions of the dura or parenchyma. 15 The background lacks the typical fibrotic stroma and may show reactive astrocytic proliferation with prominent Rosenthal formation, obscuring the ...
Sinus Histiocytosis - an overview ScienceDirect Topics
WebThe reactive histiocytic disorders are a group of diseases characterized by a systemic or localized proliferation of benign histiocytes. In virus-associated hemophagocytic syndrome and X-linked lymphoproliferative syndrome, the histiocytic proliferation occurs following an in- fectious disease. WebA histiocyte is a differentiated tissue cell that has its origin in the bone marrow. The source for histiocytes is the monocyte / macrophage line. Monocytes (found in the blood) and … city cars pretoria
Dermatopathology. Inflammatory skin diseases DermNet
WebThe reactive histiocytic disorders are a group of diseases characterized by a systemic or localized proliferation of benign histiocytes. In virus-associated hemophagocytic syndrome and X-linked lymphoproliferative syndrome, the histiocytic proliferation occurs following an in- fectious disease. WebThe pathology demonstrated extensive areas of chronic inflammation with epithelioid histiocytes, reactive pneumocytes, chronic interstitial inflammation, poorly formed non-caseating granulomas, no fibrosis, and negative cytology for malignancy. CD68 highlights admixed histiocytes (Figures (Figures2a, 2a, ,2b). 2b). city cars poki