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自愈性网状组织细胞增生症:文献中第四例病例的临床、组织学及超微结构研究

Self-healing reticulohistiocytosis: a clinical, histologic, and ultrastructural study of the fourth case in the literature.

作者信息

Hashimoto K, Griffin D, Kohsbaki M

出版信息

Cancer. 1982 Jan 15;49(2):331-7. doi: 10.1002/1097-0142(19820115)49:2<331::aid-cncr2820490220>3.0.co;2-5.

Abstract

A case of self-healing reticulohistiocytosis is reported. Our case differed from those previously reported in that tumors developed 17 days after birth (instead of at birth) and all tumors disappeared rapidly within three weeks (instead of two to three and one-half months). Hematologic abnormalities such as absolute neutropenia, marked lymphocytosis with many atypical cells, and atypical monocytes in bone marrow in association with this disease have not previously been reported. The patient had palpable liver which persisted with absolute neutropenia for about a month. The diagnosis of self-healing reticulohistiocytosis was confirmed by characteristic histology and by the demonstration of Langerhans' cells with typical granules in the tumor cells.

摘要

报告了一例自愈性网状组织细胞增多症病例。我们的病例与先前报道的病例不同之处在于,肿瘤在出生后17天(而非出生时)出现,并且所有肿瘤在三周内迅速消失(而非两到三个半月)。此前尚未报道过与该疾病相关的血液学异常,如绝对中性粒细胞减少、伴有许多非典型细胞的明显淋巴细胞增多以及骨髓中的非典型单核细胞。患者肝脏可触及,伴有绝对中性粒细胞减少持续约一个月。通过特征性组织学检查以及在肿瘤细胞中发现具有典型颗粒的朗格汉斯细胞,确诊为自愈性网状组织细胞增多症。

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