Head and neck synovial sarcoma in a woman with previous lymphoma and papillary thyroid carcinoma.

IF 4.4 Q1 PATHOLOGY
Mariano Lombardi, Daniela Lepanto, Eleonora Pisa, Valeria Midolo De Luca, Renato Lobrano, Simona Pessina, Chiara Zanetti, Marta Tagliabue, Elvio De Fiori, Fausto Maffini
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引用次数: 0

Abstract

Synovial sarcoma is a rare malignant mesenchymal neoplasm that rarely arises in the head and neck and thyroid lodge. Researchers have documented only few cases in the literature. We present the case of a young woman diagnosed with synovial sarcoma that originated in the thyroid region one year after a total thyroidectomy for a primary papillary carcinoma and eight years after chemo-radiotherapy for a lymphoma.

头颈部滑膜肉瘤1例既往有淋巴瘤和甲状腺乳头状癌。
滑膜肉瘤是一种罕见的恶性间质肿瘤,很少发生在头颈部和甲状腺部位。研究人员在文献中只记录了少数病例。我们提出一个病例的年轻女性诊断为滑膜肉瘤起源于甲状腺区域,一年后全甲状腺切除术的原发性乳头状癌和化疗后八年的淋巴瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
PATHOLOGICA
PATHOLOGICA PATHOLOGY-
CiteScore
5.90
自引率
5.70%
发文量
108
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