手术难治的炎性肌纤维母细胞瘤：肺部罕见肿瘤

IF 0.7 Q3 Medicine ASIAN CARDIOVASCULAR & THORACIC ANNALS Pub Date : 2024-09-01 Epub Date: 2024-05-01 DOI:10.1177/02184923241248681

Nirupam Sekhar Chakraborty, Gaind Kumar Saurav, Nitin Kashyap, Pranay Mehsare Suresh, Nitin Borkar, Rakesh Gupta

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引用次数: 0

摘要

炎性肌纤维母细胞瘤被认为是最罕见的良性肿瘤之一，占所有肺肿瘤的 0.7%。它于 1939 年首次被描述。我们报告了一例 10 岁儿童的病例，患者反复咳嗽和发烧。胸片和计算机断层扫描显示肿瘤完全累及右肺。我们将肿瘤连同受影响的肺部从周围结构中小心翼翼地剥离出来，然后送到室外。标本的组织病理学检查显示它是炎性成纤维细胞瘤。

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Surgically challenging inflammatory myofibroblastic tumor: A rare neoplasm of lung.

Inflammatory myofibroblastic tumor is considered one of the rarest benign tumors constituting 0.7% of all lung neoplasms. It was first described in 1939. We report a case of a 10-year-old child who presented with recurrent cough and fever. Chest radiography and computed tomography demonstrated complete involvement of right lung by the tumor. The tumor along with the affected lung was meticulously dissected from the surrounding structures and was delivered outside. The histopathology of the specimen revealed it to be inflammatory fibroblastoma.

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来源期刊

ASIAN CARDIOVASCULAR & THORACIC ANNALS Multiple-

CiteScore

1.30

自引率

0.00%

发文量

期刊介绍： The Asian Cardiovascular and Thoracic Annals is an international peer-reviewed journal pertaining to cardiovascular and thoracic medicine. Besides original clinical manuscripts, we welcome research reports, product reviews, reports of new techniques, and findings of special significance to Asia and the Pacific Rim. Case studies that have significant novel original observations, are instructive, include adequate methodological details and provide conclusions. Workshop proceedings, meetings and book reviews, letters to the editor, and meeting announcements are encouraged along with relevant articles from authors.