Langerhans cell histiocytosis of the thyroid

被引:2
|
作者
Oudidi, A. [1 ]
Hachimi, Hicham [1 ]
El Alami, Med Nourredine [1 ]
机构
[1] CHU Hassan II, Serv ORL, Fes, Morocco
来源
PRESSE MEDICALE | 2006年 / 35卷 / 06期
关键词
D O I
10.1016/S0755-4982(06)74731-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction > Langerhans cell histiocytosis, also known as histiocytosis X, has a broad clinical spectrum and highly variable prognosis. Its localization in the thyroid gland is relatively rare and presents particular diagnostic and therapeutic difficulties. Case > A 38-year-old man consulted for on anterior cervical moss that doted back to childhood but which had grown substantially in volume over the post seven months. The workup indicated a left thyroid nodule. We performed a thyroid lobectomy with isthmusectomy Immunohistochemical and pathology analyses showed Langerhans cell histiocytosis of the thyroid. The immediate postoperative course and subsequent outcome were good (follow-up: 34 months). Conclusion > Diagnosis and treatment of Langerhans cell histiocytosis in the thyroid gland often require multidisciplinary cooperation to analyze clinical, radiological, and pathology findings.
引用
收藏
页码:977 / 979
页数:3
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