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孤立性结外窦组织细胞增多症表现为髓内脊髓肿瘤并导致截瘫。病例报告。

Isolated extranodal sinus histiocytosis presenting as an intramedullary spinal cord tumor with paraplegia. Case report.

作者信息

Osenbach R K

机构信息

Division of Neurosurgery, Walter Reed Army Medical Center, Washington, District of Columbia.

出版信息

J Neurosurg. 1996 Oct;85(4):692-6. doi: 10.3171/jns.1996.85.4.0692.

Abstract

Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease) is a nonneoplastic lymphoproliferative disorder that usually presents with massive painless cervical lymphadenopathy accompanied by fever and weight loss. Extranodal involvement occurs in over 40% of patients; however, isolated extranodal disease without lymph node involvement is unusual. Extranodal involvement of the nervous system is unusual and isolated central nervous system disease in the absence of nodal disease is distinctly rare. The author describes the case of a 35-year-old man who presented with paraplegia and an enhancing intramedullary lesion on magnetic resonance imaging that was suggestive of a primary spinal cord tumor. The lesion was completely resected and histologically proved to be consistent with an isolated extranodal case of Rosai-Dorfman disease. Although a number of cases of this entity involving the CNS have been published, the author believes this case represents the first report of intramedullary spinal cord involvement as the initial and only sign of disease.

摘要

伴巨大淋巴结病的窦性组织细胞增生症(罗萨伊-多夫曼病)是一种非肿瘤性淋巴增殖性疾病,通常表现为巨大无痛性颈部淋巴结病,并伴有发热和体重减轻。超过40%的患者会出现结外受累;然而,无淋巴结受累的孤立性结外疾病并不常见。神经系统的结外受累并不常见,而无淋巴结疾病的孤立性中枢神经系统疾病则极为罕见。作者描述了一名35岁男性的病例,该患者出现截瘫,磁共振成像显示髓内病变强化,提示原发性脊髓肿瘤。病变被完全切除,组织学检查证实与罗萨伊-多夫曼病的孤立性结外病例一致。尽管已经发表了许多涉及中枢神经系统的该实体病例,但作者认为该病例代表了脊髓髓内受累作为疾病初始和唯一表现的首例报告。

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