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Primary endobronchial myxoid leiomyoma in a child: An unusual case report and review of literature.

作者信息

Awasthi Ashutosh, Dubey Suparna, Sabhikhi Abha K, Bal Sabyasachi

机构信息

Department of Pathology, School of Medical Sciences and Research, Sharda University, Uttar Pradesh, India.

出版信息

Indian J Pathol Microbiol. 2016 Jan-Mar;59(1):87-9. doi: 10.4103/0377-4929.174830.

DOI:10.4103/0377-4929.174830
PMID:26960646
Abstract

Primary leiomyomas are rare benign tumors of the lung and only 25 cases have been documented in children, most of which are endobronchial. Leiomyomas are benign smooth muscle neoplasms, usually diagnosed on morphological characteristics. However, immunohistochemistry plays a crucial role in the lineage differentiation when these are encountered at unusual sites or with unexpected morphological features. We report a case of endobronchial tumor of a 13-year-old male child who presented with a dry cough and hemoptysis. A mass lesion in the right main bronchus was detected by bronchoscopy and contrast-enhanced computed tomography. On histopathological examination of the resected specimen, a diagnosis of myxoid leiomyoma was made. To the best of our knowledge, this is the first case of myxoid leiomyoma to be reported in the respiratory tract. This case also demonstrates the need for a high index of suspicion and the role of immunomarkers in the diagnosis of such challenging cases.

摘要

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Primary endobronchial myxoid leiomyoma in a child: An unusual case report and review of literature.
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引用本文的文献

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Endobronchial Smooth Muscle Tumors: A Series of Five Cases Highlighting Pitfalls in Diagnosis.支气管内平滑肌肿瘤:5例系列病例凸显诊断中的陷阱
J Pathol Transl Med. 2018 Jul;52(4):219-225. doi: 10.4132/jptm.2018.05.16. Epub 2018 Jul 11.
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