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肺罕见的腔隙性淋巴上皮样癌:临床经验和文献复习。

Rare cavitary lymphoepithelioma-like carcinoma of lung: clinical experience and literature review.

机构信息

Department of Radiology, Medical Imaging Center of Guizhou Province, the Affiliated Hospital of Zunyi Medical University, Zunyi, 563000, China.

出版信息

BMC Pulm Med. 2023 Jul 5;23(1):246. doi: 10.1186/s12890-023-02529-x.

Abstract

BACKGROUND

Lymphoepithelioma-like carcinoma of the lung is a rare primary malignancy of the lung, accounting for only 0.9% of primary malignancies of the lung. Those associated with cavities are even rarer, with fewer than five cases reported in the English literature. Concurrently, the imaging findings of tumors are usually non-specific, resulting in insufficient understanding of the disease by clinicians, thus leading to misdiagnosis and delayed treatment.

CASE PRESENTATION

A 42-year-old female presented with a right lower lung mass with cavities. First identified on chest computed tomography (CT) in 2021, the mass persisted for 1 year and subsequently enlarged on chemotherapy and routine follow-up CT. Right lower lobectomy was then performed. Postoperative pathology confirmed primary pulmonary lymphoepithelioma-like carcinoma. After 10 months of follow-up, the patient was still alive and no recurrence was observed.

CONCLUSIONS

This article aims to describe a rare case of cavitary lymphoepithelioma-like carcinoma of the lung and review it clinical and imaging characteristics reported in previous cases, which will be helpful for clinicians and imaging physicians in diagnosing this disease.

摘要

背景

肺淋巴上皮瘤样癌是一种罕见的肺部原发性恶性肿瘤,仅占肺部原发性恶性肿瘤的 0.9%。与空洞相关的则更为罕见,英文文献中报道的病例不足 5 例。同时,肿瘤的影像学表现通常不具有特异性,导致临床医生对该疾病认识不足,从而导致误诊和治疗延误。

病例介绍

一名 42 岁女性因右下肺肿块伴空洞就诊。该患者于 2021 年首次在胸部 CT 上发现肿块,肿块持续存在 1 年,随后在化疗和常规随访 CT 上增大。随后行右下肺叶切除术。术后病理证实为原发性肺淋巴上皮瘤样癌。随访 10 个月后,患者仍存活,未观察到复发。

结论

本文旨在描述一例罕见的肺空洞性淋巴上皮瘤样癌,并回顾既往病例报道的其临床和影像学特征,这将有助于临床医生和影像医师对该病的诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c01/10324186/e31b67e122ff/12890_2023_2529_Fig1_HTML.jpg

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