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伴有双侧眼部受累的Rosai-Dorfman病的结外表现。

Extranodal manifestation of Rosai-Dorfman disease with bilateral ocular involvement.

作者信息

Kala Chayanika, Agarwal Asha, Kala Sanjay

机构信息

Departments of Pathology, G.S.V.M. Medical College, Kanpur, India.

出版信息

J Cytol. 2011 Jul;28(3):131-3. doi: 10.4103/0970-9371.83473.

Abstract

Rosai-Dorfman disease, that is, sinus histiocytosis with massive lymphadenopathy is a benign systemic proliferative disorder of histiocytes. The typical clinical presentation of the disease includes bilateral painless massive lymphadenopathy, fever and polyclonal hypergammaglobulinemia. Extranodal involvement is present in only a few cases and skin lesions are the most common form of extranodal disease. However, purely cutaneous Rosai-Dorfman disease is uncommon. In this study, we describe a 10-year-old child presenting with bilateral ocular involvement.

摘要

罗萨伊-多夫曼病,即伴有巨大淋巴结病的窦性组织细胞增多症,是一种组织细胞的良性全身性增殖性疾病。该疾病的典型临床表现包括双侧无痛性巨大淋巴结病、发热和多克隆高球蛋白血症。仅少数病例存在结外受累,皮肤病变是结外疾病最常见的形式。然而,单纯皮肤型罗萨伊-多夫曼病并不常见。在本研究中,我们描述了一名出现双侧眼部受累的10岁儿童。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/183b/3159292/f8f205304c3a/JCytol-28-131-g001.jpg

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