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伴有巨大淋巴结病的窦性组织细胞增多症,酷似亚急性甲状腺炎。

Sinus histiocytosis with massive lymphadenopathy simulating subacute thyroiditis.

作者信息

Larkin D F, Dervan P A, Munnelly J, Finucane J

出版信息

Hum Pathol. 1986 Mar;17(3):321-4. doi: 10.1016/s0046-8177(83)80228-7.

DOI:10.1016/s0046-8177(83)80228-7
PMID:3512416
Abstract

A white woman who had sinus histiocytosis with massive lymphoadenopathy (SHML) presented with a painful goiter and tender cervical lymph nodes. She had biochemical evidence of hypothyroidism but remained clinically euthyroid. Histologic examination confirmed SHML in the thyroid and cervical lymph nodes. The disease remitted spontaneously.

摘要

一名患有窦性组织细胞增多症伴巨大淋巴结病(SHML)的白人女性出现疼痛性甲状腺肿和颈部淋巴结压痛。她有甲状腺功能减退的生化证据,但临床上仍处于甲状腺功能正常状态。组织学检查证实甲状腺和颈部淋巴结存在SHML。该病自发缓解。

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Sinus histiocytosis with massive lymphadenopathy simulating subacute thyroiditis.伴有巨大淋巴结病的窦性组织细胞增多症,酷似亚急性甲状腺炎。
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引用本文的文献

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[Extranodal Rosai Dorfman disease (sinus histiocytosis with massive lymphadenopathy). Report of 5 cases].[结外Rosai-Dorfman病(伴巨大淋巴结病的窦组织细胞增生症)。5例报告]
Pathologe. 2004 May;25(3):222-8. doi: 10.1007/s00292-003-0642-9.
2
Cold thyroid nodule as the sole manifestation of Rosai-Dorfman disease with mild lymphadenopathy, coexisting with chronic autoimmune thyroiditis.冷甲状腺结节作为罗萨伊-多夫曼病的唯一表现,伴有轻度淋巴结病,与慢性自身免疫性甲状腺炎并存。
J Endocrinol Invest. 1999 Dec;22(11):866-70. doi: 10.1007/BF03343661.
3
Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease).
Pediatr Radiol. 1990;20(6):425-32. doi: 10.1007/BF02075199.