Yousem S A
Arch Pathol Lab Med. 1986 Feb;110(2):112-5.
Three cases of angiosarcoma presenting as diffuse pulmonary infiltrates are described and the clinical presentations, histologic findings, and differential diagnosis are discussed. Primary pulmonary angiosarcomas are extremely rare and require careful clinical evaluation to exclude metastases from the heart, pericardium, pulmonary arterial trunk, and distant extrathoracic sites.
本文描述了三例表现为弥漫性肺浸润的血管肉瘤病例，并讨论了其临床表现、组织学特征及鉴别诊断。原发性肺血管肉瘤极为罕见，需要进行仔细的临床评估以排除来自心脏、心包、肺动脉主干及远处胸外部位的转移瘤。
