Wenig B M, Abbondanzo S L, Heffess C S
Department of Otolaryngic-Endocrine Pathology, Armed Forces Institute of Pathology, Washington, DC 20306-6000.
Am J Surg Pathol. 1994 Jan;18(1):62-73.
Adrenal epithelioid angiosarcomas (AEA) are rare neoplasms. We report the clinicopathologic features of nine cases of AEA. AEA occurred most frequently in the sixth and seventh decades of life (age range, 45-85 years; median, 60); five cases occurred in men and four in women. Presenting symptoms included abdominal mass with or without pain, weight loss, fever, and weakness. Two cases were asymptomatic; one was discovered during evaluation for other disease(s) and the other at autopsy. All neoplasms were nonfunctioning. Radiographic evaluation demonstrated suprarenal or retroperitoneal neoplasms ranging in size from 6 to 10 cm in greatest dimension. Histologically, the neoplasms were invasive, predominantly arranged in solid sheets or nests, and composed of epithelioid cells. Endothelial cell differentiation was suggested by the transition areas between dilated anastomotic vascular spaces and the sheet-like growth, the cytomorphologic similarity between the endothelial cells lining the discernible vascular spaces and those seen in the solid foci, and the presence of intracytoplasmic vacuolization occasionally containing red blood cells. Endothelial derivation was confirmed by immunohistochemistry including Factor VIII-related antigen (FVIII), CD-34 (hematopoetic progenitor cell antigen), and/or Ulex europaeus agglutinin-1 lectin immunoreactivity (UEA-1) and by ultrastructural findings, including rod-shaped microtubulated bodies and intracytoplasmic lumen formation. In addition, cytokeratin reactivity was seen in seven cases, and B72.3 (tumor-associated glycoprotein-72) reactivity was seen in six. Surgical resection was the treatment of choice, occasionally supplemented by chemotherapy. Three patients are presently alive, free of disease, at 13, 11, and 6 years following diagnosis. Three died with metastatic AEA of the lung, and three died of unrelated causes.
肾上腺上皮样血管肉瘤(AEA)是一种罕见的肿瘤。我们报告了9例AEA的临床病理特征。AEA最常发生于60至70岁(年龄范围45 - 85岁;中位数60岁);5例发生于男性,4例发生于女性。主要症状包括伴有或不伴有疼痛的腹部肿块、体重减轻、发热和虚弱。2例无症状;1例在评估其他疾病时发现,另1例在尸检时发现。所有肿瘤均无功能。影像学评估显示肾上腺或腹膜后肿瘤,最大直径为6至10厘米。组织学上,肿瘤具有侵袭性,主要呈实性片状或巢状排列,由上皮样细胞组成。扩张的吻合血管腔隙与片状生长之间的过渡区域、可识别血管腔内衬的内皮细胞与实性病灶中所见内皮细胞的细胞形态相似性以及偶尔含有红细胞的胞质空泡化提示内皮细胞分化。通过包括因子VIII相关抗原(FVIII)、CD - 34(造血祖细胞抗原)和/或荆豆凝集素 - 1凝集素免疫反应性(UEA - 1)的免疫组化以及包括杆状微管状体和胞质内腔形成的超微结构发现证实了内皮来源。此外,7例可见细胞角蛋白反应性,6例可见B72.3(肿瘤相关糖蛋白 - 72)反应性。手术切除是首选治疗方法,偶尔辅以化疗。3例患者目前存活,诊断后13年、11年和6年无疾病。3例死于肺转移性AEA,3例死于无关原因。