Department of Surgery, University of Pavia, Division of Hepato-Pancreatic Surgery, Pavia, Italy.
Pathol Int. 2009 Dec;59(12):890-4. doi: 10.1111/j.1440-1827.2009.02461.x.
Reported herein is an unusual vascular tumor primary arising in the liver and exhibiting unique histopathological features. A 47-year-old woman underwent left hepatectomy because of a large hepatic mass. On histology the tumor had a composite pattern, consisting of angiomatous, retiform and solid areas, formed by oval to cuboidal to spindle cells, that expressed only endothelial markers (CD31 and factor VIII-related antigen). These findings led to the diagnosis of a low-grade vascular neoplasm with morphological features consistent with so-called polymorphous hemangioendothelioma. The tumor was completely resected. At 24 month follow up the patient was alive, without evidence of disease. Polymorphous hemangioendothelioma is a rare vascular neoplasm, with borderline malignant potential, which usually occurs in lymph nodes and, rarely, at extranodal sites. Its classification as an entity has been questioned recently. The unusual morphological features of the present case, which do not fit neatly with any other recognized hemangioendothelioma subtype, indicate that the family of vascular tumors is broader than currently accepted. In addition the present case widens the spectrum of primary vascular tumors arising in the liver.
本文报道了一例罕见的肝脏原发性血管肿瘤,具有独特的组织病理学特征。一名 47 岁女性因巨大肝肿块而行左半肝切除术。组织学上,肿瘤呈复合模式,由血管状、网状和实性区域组成,由卵圆形、立方状至梭形细胞构成,仅表达内皮细胞标志物(CD31 和 VIII 因子相关抗原)。这些发现提示诊断为低度血管性肿瘤,其形态特征与所谓的多形性血管内皮细胞瘤一致。肿瘤完全切除。随访 24 个月时,患者无病生存。多形性血管内皮细胞瘤是一种罕见的具有交界恶性潜能的血管性肿瘤,通常发生在淋巴结,很少发生在结外部位。最近有人对其分类提出了质疑。本例的不典型形态学特征与任何其他已识别的血管内皮细胞瘤亚型都不相符,表明血管肿瘤家族比目前公认的更为广泛。此外,本例还扩大了肝脏原发性血管肿瘤的范围。