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原发性肺上皮样血管肉瘤:双侧气胸的罕见病例报告

Primary Pulmonary Epithelioid Angiosarcoma: A Rare Case Presentation of Bilateral Pneumothoraces.

作者信息

Faiek Saif, Tariq Hafsa, Upparapalli Deepti, Bansal Aditya, Sompalli Sreeja

机构信息

Internal Medicine, AtlantiCare Regional Medical Center, Atlantic City, USA.

Critical Care Medicine, AtlantiCare Regional Medical Center, Atlantic City, USA.

出版信息

Cureus. 2019 Dec 30;11(12):e6514. doi: 10.7759/cureus.6514.

Abstract

Angiosarcoma is a rare malignant neoplasm with a very poor prognosis that originates from the vascular endothelium and accounts for only 1%-2% of all sarcomatous malignancies. It is most commonly present in the deep soft tissues. Still, a wide range of primary sites, including the adrenals, thyroid, skin, and bone, are encountered. Here, we report a 52-year-old female with a past medical history of hypertension who presented with chest pain. Her chest images showed bilateral pneumothoraces with diffuse cystic lung disease. She underwent bilateral video-assisted thoracoscopy with a tissue biopsy, which was consistent with epithelioid angiosarcoma.

摘要

血管肉瘤是一种罕见的恶性肿瘤,预后极差,起源于血管内皮,仅占所有肉瘤性恶性肿瘤的1%-2%。它最常出现在深部软组织中。不过,也会出现在包括肾上腺、甲状腺、皮肤和骨骼在内的广泛原发部位。在此,我们报告一名52岁女性,有高血压病史,出现胸痛症状。她的胸部影像显示双侧气胸伴弥漫性囊性肺病。她接受了双侧电视辅助胸腔镜检查及组织活检,结果符合上皮样血管肉瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae1d/6988729/9146374d6ddd/cureus-0011-00000006514-i01.jpg

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