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血管内细支气管肺泡瘤:一种独特的外科和病理实体。

Intravascular bronchioloalveolar tumor: a distinctive surgical and pathological entity.

作者信息

Sweeney W B, Vesoulis Z, Blaum L C

出版信息

Ann Thorac Surg. 1986 Dec;42(6):702-4. doi: 10.1016/s0003-4975(10)64615-2.

Abstract

A patient with intravascular bronchioloalveolar tumor is described, and the clinical and pathological characteristics of the tumor are discussed. So-called intravascular bronchioloalveolar tumor (IVBAT) is a relatively new, but well-recognized lung neoplasm. This tumor is a lung neoplasm of distinctive histogenesis newly incorporated into the World Health Organization histologic typing of lung tumors under the category "miscellaneous tumors, malignant." The importance of the neoplasm is that it is rarely recognized clinically and frequently misdiagnosed. Awareness of this lesion can be enhanced by recognizing its particular clinical presentation, surgical appearance, and unique histopathologic factors.

摘要

本文描述了一例血管内细支气管肺泡瘤患者,并讨论了该肿瘤的临床和病理特征。所谓的血管内细支气管肺泡瘤(IVBAT)是一种相对较新但已被充分认识的肺肿瘤。这种肿瘤是一种具有独特组织发生的肺肿瘤,最近被纳入世界卫生组织肺肿瘤组织学分类中的“其他肿瘤,恶性”类别。该肿瘤的重要性在于其在临床上很少被认识,且经常被误诊。通过认识其特殊的临床表现、手术外观和独特的组织病理学特征,可以提高对这种病变的认识。

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