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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.

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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