Electron microscopic study of the orbital lesion of Hand-Schüller-Christian disease.

Journal of pediatric ophthalmology Pub Date : 1977-07-01
T Amemiya, H Yoshida
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Abstract

The orbital bone lesion of a patient with Hand-Schüller-Christian disease was examined by electron microscopy. Vacuoles in the cytoplasm of foam cells contained granules which were shown by histochemical examination to be cholesterin. Langerhans cell granules in the histiocytes of Hand-Schüller-Christian disease showed a close resemblance to those in Langerhans cell of the epidermis, eosinophilic granuloma and Letterer-Siwe disease. Charcot-Leyden crystals appeared to be formed in the lysosomes of histiocytes in Hand-Schüller-Christian disease. From histopathological and cytological points of view, eosinophilic granuloma, Hand-Schüller-Christian disease and Letterer-Siwe disease are classified as histiocytosis X. The simultaneous appearance of Langerhans cell granules and Charcot-Leyden crystals is specific in histiocytosis X.

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hand - schller - christian病眼眶病变的电镜研究。
本文用电子显微镜检查了一例hand - schller - christian病的眶骨病变。泡沫细胞胞浆中的空泡中含有颗粒,经组织化学检查为胆固醇。hand - schller - christian病组织细胞中的朗格汉斯细胞颗粒与表皮、嗜酸性肉芽肿和letter - siwe病的朗格汉斯细胞颗粒非常相似。在hand - schller - christian病中,组织细胞溶酶体中似乎形成Charcot-Leyden晶体。从组织病理学和细胞学角度看,嗜酸性肉芽肿、hand - schller - christian病和letter - siwe病属于组织细胞增多症X。朗格汉斯细胞颗粒和charco - leyden晶体同时出现是组织细胞增多症X的特异性表现。
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Congenital ocular anomalies in Pondicherry. Retinal involvement in tuberous sclerosis. Mesoectodermal dysgenesis: familial iris anomaly. A modified Schirmer test: the fine-thread method for measuring lacrimation. Hallermann-Streiff-Francois syndrome.
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