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肝血管肉瘤:临床病理特征和形态学模式。

Angiosarcoma of the Liver: Clinicopathologic Features and Morphologic Patterns.

机构信息

Division of Anatomic Pathology, Mayo Clinic, Rochester, MN.

出版信息

Am J Surg Pathol. 2019 May;43(5):581-590. doi: 10.1097/PAS.0000000000001228.

Abstract

Angiosarcoma is a rare malignant neoplasm of the liver. The various morphologic patterns seen with angiosarcomas of the liver have not been systematically studied and their recognition remains a major diagnostic challenge. In order to provide more comprehensive data on the morphologic patterns, angiosarcomas that had been diagnosed between 1996 and 2016 at a large medical referral center were reviewed. The major growth patterns were classified as sinusoidal (non-mass forming) versus mass forming. The mass-forming cases were further subdivided into epithelioid, spindled, or vasoformative. The study identified 21 patients with primary hepatic angiosarcoma: 13 men and 8 women. The ages ranged from 26 to 89 years. Seventeen angiosarcomas were mass-forming tumors, of which 9 showed predominantly vasoformative growth. Most of these vasoformative cases (6/9) were composed of small vessels, 2 cases had slit-like vascular spaces, and one case showed a mixture of small and large vessels. There were 7 mass-forming angiosarcomas without vasoformation: 3 had an epithelioid morphology and 4 were composed primarily of spindled cells. The final mass-forming tumor showed a mixture of vasoformative and nonvasoformative areas. Four of 21 cases were non-mass forming and showed either diffuse sinusoidal infiltration (N=2) or prominent peliotic changes (N=2). Finally, 3 uncommon patterns were identified. One case showed nodules of spindle cells arranged in prominent whorls in a background of loose connective tissue with abundant inflammation. A second case arose in the setting of the Blue Rubber Bleb Nevus Syndrome and showed numerous tumor nodules with an architectural pattern that resembled infantile hemangioma, some with areas of atypia consistent with malignant transformation to angiosarcoma. The third unusual pattern showed multiple nodules of thin walled large caliber vascular proliferations, some of which showed atypia that reached the level of angiosarcoma. The results from this study indicate that the majority of hepatic angiosarcomas are mass forming (two third of cases), a pattern that is recognizable on H&E when vasoformative, but can mimic carcinoma or undifferentatied sarcomas when nonvasoformative (one third of cases). The sinusoidal patterns are particularly challenging and are frequently missed on initial review. Finally, we describe several unsual patterns of angiosarcoma. Awareness of these classic and rare morphologic patterns can help make the diagnosis of angiosarcoma.

摘要

肝血管肉瘤是一种罕见的肝脏恶性肿瘤。肝血管肉瘤的各种形态模式尚未得到系统研究,其识别仍然是一个主要的诊断挑战。为了提供更多关于形态模式的全面数据,对一家大型医疗转诊中心在 1996 年至 2016 年间诊断的血管肉瘤进行了回顾性研究。主要生长模式分为窦状(非肿块形成)与肿块形成。肿块形成的病例进一步分为上皮样、梭形或血管形成。研究确定了 21 例原发性肝血管肉瘤患者:13 名男性和 8 名女性。年龄从 26 岁到 89 岁不等。17 例血管肉瘤为肿块形成肿瘤,其中 9 例表现为主要血管形成生长。这些血管形成性病例中(9/17)大多数由小血管组成,2 例有裂隙状血管腔,1 例表现为小血管和大血管混合。7 例无血管形成的肿块形成性血管肉瘤:3 例具有上皮样形态,4 例主要由梭形细胞组成。最终的肿块形成性肿瘤显示出血管形成和非血管形成区域的混合。21 例中有 4 例是非肿块形成性的,表现为弥漫性窦状浸润(N=2)或明显的海绵状变(N=2)。最后,确定了 3 种不常见的模式。1 例表现为在疏松结缔组织背景中有大量炎症的情况下,排列成明显漩涡状的梭形细胞结节。另 1 例发生在蓝色橡皮泡痣神经纤维瘤综合征中,表现为许多肿瘤结节,其结构模式类似于婴儿血管瘤,一些区域具有非典型性,符合血管肉瘤的恶性转化。第三种不常见的模式表现为多个薄壁大口径血管增生结节,其中一些结节具有异型性,达到血管肉瘤的水平。这项研究的结果表明,大多数肝血管肉瘤是肿块形成的(三分之二的病例),这种模式在 H&E 上是可识别的,如果是血管形成的,则可以识别,但如果是非血管形成的(三分之一的病例),则可以模拟癌或未分化肉瘤。窦状模式尤其具有挑战性,在初次检查时经常被遗漏。最后,我们描述了几种血管肉瘤的不常见模式。对这些经典和罕见形态模式的认识可以帮助诊断血管肉瘤。

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