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Hashimoto-Pritzker disease : ウィキペディア英語版 | Congenital self-healing reticulohistiocytosis Congenital self-healing reticulohistiocytosis (also known as "Hashimoto–Pritzker disease," and "Hashimoto–Pritzker syndrome"〔) is a condition that is a self-limited form of Langerhans cell histiocytosis. ==Symptoms== Non-specific inflammatory response, which includes fever, lethargy, and weight loss. This is suspected of being a genetic disorder, and as the name implies, is self healing. *Skin: Commonly seen are a rash which varies from scaly erythematous lesions to red papules pronounced in intertriginous areas. Up to 80% of patients have extensive eruptions on the scalp. *Lymph node: Enlargement of the lymph nodes in 50% of Histiocytosis cases.
抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)』 ■ウィキペディアで「Congenital self-healing reticulohistiocytosis」の詳細全文を読む
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