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罗萨达-多夫曼病。

Rosai-Dorfman disease.

机构信息

Department of Medicine, Medical College, 88 College Street, Kolkata 700073, India.

出版信息

Singapore Med J. 2010 Oct;51(10):e173-5.

Abstract

Sinus histiocytosis with massive lymphadenopathy, also known as Rosai-Dorfman disease, is a rare histiocytic proliferative disorder of unknown aetiology. The classic presentation of Rosai-Dorfman disease is massive, bilateral, painless cervical lymphadenopathy. Extranodal disease is also common, often with a particular predilection for the head and neck regions. We report a rare case of Rosai-Dorfman disease with nodal and multiple extranodal manifestations in a 13-year-old girl. The patient had cervical and mediastinal lymphadenopathy, multiple soft tissue swellings of the scalp, bilateral proptosis and goitre due to thyroid gland involvement. She responded to steroids, with remission of the swellings and symptoms. This case is being reported for its rarity, multiple extranodal manifestations and thyroid gland involvement. Thyroid gland involvement in Rosai-Dorfman disease has rarely been reported in the literature.

摘要

窦组织细胞增生伴巨大淋巴结病,又称 Rosai-Dorfman 病,是一种病因不明的罕见组织细胞增生性疾病。Rosai-Dorfman 病的典型表现为巨大的双侧无痛性颈淋巴结病。结外疾病也很常见,常特别倾向于头颈部。我们报告了一例罕见的 Rosai-Dorfman 病病例,该患者为 13 岁女孩,具有结内和多个结外表现。该患者患有颈淋巴结和纵隔淋巴结病,头皮多处软组织肿胀,双侧眼球突出和甲状腺受累导致甲状腺肿大。她对类固醇有反应,肿胀和症状消退。本病例报告的原因是其罕见性、多个结外表现和甲状腺受累。文献中很少有 Rosai-Dorfman 病累及甲状腺的报道。

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