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一名患有结节性硬化症和朗格汉斯细胞组织细胞增多症患者的多脏器发育异常病变

Multivisceral dysplastic lesions in a patient with tuberous sclerosis and Langerhans cell histiocytosis.

作者信息

Drut R

机构信息

Servicio de Patología, Hospital de Niños, La Plata, República Argentina.

出版信息

Pediatr Pathol. 1990;10(4):633-9. doi: 10.3109/15513819009067152.

Abstract

Collections of large cells and smaller satellite-like cells arranged in an autonomic ganglion-like pattern and resembling the white matter lesions of tuberous sclerosis were found in the thymus, lungs, liver, appendix, and heart of an 8-month-old infant who exhibited other pathologic findings of tuberous sclerosis (rhabdomyomas of the heart and multiple kidney cysts). Focal cytoplasmic staining for S-100 and GFAP was noted in some large cells, suggesting neural (probably schwannian) differentiation. Dysplastic neurogenic foci appearing in internal organs may represent another morphologic marker of tuberous sclerosis. The simultaneous presence of Langerhans cell histiocytosis produced an unusual combination not previously reported.

摘要

在一名8个月大的婴儿的胸腺、肺、肝、阑尾和心脏中发现了大量细胞和较小的卫星样细胞的集合,这些细胞呈自主神经节样排列,类似于结节性硬化症的白质病变,该婴儿还表现出结节性硬化症的其他病理表现(心脏横纹肌瘤和多个肾囊肿)。在一些大细胞中发现了S-100和GFAP的局灶性细胞质染色,提示神经(可能是雪旺氏)分化。出现在内脏器官中的发育异常的神经源性病灶可能代表结节性硬化症的另一种形态学标志物。朗格汉斯细胞组织细胞增多症的同时存在产生了一种以前未报道过的不寻常组合。

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