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病例报告:一名左上叶先天性发育不全患者的黏液表皮样癌。

Case report: Mucoepidermoid carcinoma in a patient with congenital agenesis of the left upper lobe.

作者信息

Pandya H, Matthews S

机构信息

Department of Radiology, Northern General Hospital, Herries Road, Sheffield S5 7AU, UK.

出版信息

Br J Radiol. 2003 May;76(905):339-42. doi: 10.1259/bjr/29778480.

Abstract

This report describes an unusual case of a mucoepidermoid carcinoma developing in a patient with congenital left upper lobe agenesis. Mucoepidermoid tumours most often develop in major bronchi and present as lobar collapse, post-obstructive pneumonia or as a mass lesion on chest radiography. On CT, the tumour is smooth, well defined, homogeneous and may enhance with intravenous contrast. Tumour calcification has been reported. Lobar agenesis often presents as a co-incidental finding on chest radiography as total or almost complete absence of aeration of the affected lung. Thoracic CT confirms the presence of the underdeveloped lung, pulmonary artery and bronchus and associated mediastinal shift and herniation of the contralateral lung. A literature review of these two conditions is presented.

摘要

本报告描述了一例先天性左肺上叶发育不全患者发生黏液表皮样癌的罕见病例。黏液表皮样肿瘤最常发生于主支气管,胸部X线表现为肺叶萎陷、阻塞性肺炎或肿块病变。CT上,肿瘤边界光滑、清晰,密度均匀,静脉注射造影剂后可强化。有肿瘤钙化的报道。肺叶发育不全在胸部X线检查时常为偶然发现,表现为患侧肺完全或几乎完全无气体充盈。胸部CT可证实发育不全的肺、肺动脉和支气管的存在,以及相关的纵隔移位和对侧肺疝。本文对这两种情况进行了文献综述。

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