朗格汉斯细胞组织细胞增多症与甲状腺乳头状癌并存

J. Bakshi, A. Goyal
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引用次数: 0

摘要

朗格汉斯细胞组织细胞增生症(LCH)是一种病因不明的罕见疾病,其特征是受影响组织中大量朗格汉斯细胞浸润导致肉芽肿的形成。在本章中,我们讨论了一例31岁男性甲状腺肿大,弥漫性坚硬,非压痛,非移动性肿胀,表现为朗格汉斯细胞组织细胞增多症与甲状腺乳头状癌(PTC)相关。甲状腺表现为朗格汉斯细胞组织细胞增多症,细针穿刺细胞学证实。对患者进行了检查,未发现结构性干预的迹象。在长春花碱和依托泊苷化疗10个周期后,肿胀程度没有减少。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Langerhans Cell Histiocytosis Co-existing with Papillary Carcinoma of Thyroid
Langerhans cell histiocytosis (LCH) is a rare condition with unknown causes and is characterized by the infiltration of significant numbers of Langerhans cells in the affected tissues leading to formation of granulomas. In this chapter, we have discussed the case of a 31-year-old man with a swollen, diffusely firm, non-tender, non-mobile thyroid swelling presented with Langerhans cell histiocytosis associated with papillary thyroid carcinoma (PTC). The thyroid was shown to be involved by langerhans cell histiocytosis, confirmed with fine needle aspiration cytology. The patient was examined, and no signs of structural intervention were discovered. After ten cycles of vinblastine and etoposide chemotherapy, there was no reduction in the extent of the swelling observed.
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