Jamaati Hamid Reza, Shadmehr Mohammad Behgam, Saidi Bahare, Khosravi Adnan, Arab Mehrdad, Mohammadi Forouzan
Department of Internal Medicine, National Research Institute of Tuberculosis and Lung Disease (NRITLD), Masih Daneshvari Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Endocr Pathol. 2009 Summer;20(2):133-6. doi: 10.1007/s12022-009-9068-0.
A 24-year-old man presented to our center with a huge goiter compressing his airway. He had a previous diagnosis of Langerhans cell histiocytosis (LCH) of the lung. Core needle biopsy was consistent with histiocytosis. Thyroidectomy was performed. A very invasive mass was encountered at the time of surgery. Histopathology result was consistent with an invasive papillary cancer of thyroid co-occurring with LCH. Although association of LCH with different malignancies has been reported, co-existing invasive papillary thyroid cancer and LCH is a rare combination.
一名24岁男性因巨大甲状腺肿压迫气道前来我院就诊。他曾被诊断为肺部朗格汉斯细胞组织细胞增多症(LCH)。粗针活检结果符合组织细胞增多症。遂行甲状腺切除术。手术中发现一个极具侵袭性的肿物。组织病理学结果显示为侵袭性甲状腺乳头状癌合并LCH。虽然已有LCH与不同恶性肿瘤相关联的报道,但侵袭性甲状腺乳头状癌与LCH并存是一种罕见的组合。