Jang Kyu Yun, Jin Gong Yong, Lee Yong Chul, Lee Hung Bum, Kang Myoung Jae, Choi Ho Yeul, Chung Myoung Ja
5th Criminal Division, Daegu District Public Prosecutor's Office, Daegu, Korea.
J Korean Med Sci. 2003 Aug;18(4):599-602. doi: 10.3346/jkms.2003.18.4.599.
Pulmonary epithelioid hemangioendothelioma (PEH) is a rare tumor that occurs among young women and typically presents as bilateral multiple nodules. In the present report, we describe an uncommon case of PEH presented as a single cavitary nodule in a 33-yr-old asymptomatic man. This is the first case of PEH presented as a single cavitary nodule in the English literature. Three years of the follow-up without treatment was performed. Overall histologic findings were accord with conventional PEH, but some atypical features such as, increased mitotic activity (mean; two per ten high power fields), necrosis, spindling, and pleural and vascular invasion were recognized. Immunohistochemically, the tumor cells were positive for CD34. This report may contribute to the data on clinical findings and natural history of this rare tumor.
肺上皮样血管内皮瘤(PEH)是一种罕见肿瘤,多见于年轻女性,通常表现为双侧多发结节。在本报告中,我们描述了一例罕见的PEH病例,该病例为一名33岁无症状男性,表现为单个空洞性结节。这是英文文献中首例表现为单个空洞性结节的PEH病例。我们对该患者进行了三年的随访,期间未进行治疗。总体组织学表现符合传统PEH,但也发现了一些非典型特征,如有丝分裂活性增加(平均每十个高倍视野两个)、坏死、梭形变以及胸膜和血管侵犯。免疫组化显示,肿瘤细胞CD34呈阳性。本报告可能有助于丰富这种罕见肿瘤的临床发现和自然史数据。