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鼻部伪装成血管瘤的看似平淡的皮肤血管肉瘤——临床病理及免疫组化分析

Deceptively bland cutaneous angiosarcoma on the nose mimicking hemangioma-A clinicopathologic and immunohistochemical analysis.

作者信息

Mitteldorf Christina, Llamas-Velasco Mar, Schulze Hans-Joachim, Thoms Kai-Martin, Mentzel Thomas, Tronnier Michael, Kutzner Heinz

机构信息

Department of Dermatology, Venereology and Allergology, HELIOS-Klinikum Hildesheim, Hildesheim, Germany.

Clinic of Dermatology, Venereology and Allergology, University Medical Center Göttingen, Germany.

出版信息

J Cutan Pathol. 2018 May 15. doi: 10.1111/cup.13275.

Abstract

BACKGROUND

We investigated 2 cases of deceptively bland cutaneous angiosarcoma (AS), which showed a uniform clinical presentation with a rapidly growing tumor on the nose. It remains unclear whether this was a primary cutaneous manifestation or a metastasis. Both tumors initially presented a high histologic overlap with a benign vascular tumor. The diagnosis was primarily based on the rapidly progressing clinical course and on the results of the staging procedures.

METHODS

Immunohistochemical stains were performed for cytokeratin (AE1/AE3 and MNF116), CD31, ERG, CD34 (HPCA1/my10), D2-40/podoplanin, LYVE-1, Ki67, PHH3, αSMA (1A4), MYC, FOS-B, CAMTA-1, TFE-3, WT1, nestin, VEGFR-2(KDR), VEGFR-3(FLT4), HHV8. MYC amplification was also investigated by fluorescence in situ hybridization.

RESULTS

The tumor cells were negative for MYC and revealed no D2-40/podoplanin expression. SMA-positive pericytes formed rims around the vessel. The proliferative activity (Ki-67) was elevated, in one case only in a later stage.

DISCUSSION

Cutaneous ASs can be rather bland and may easily be mistaken for benign vascular tumors. Both cases presented a uniform clinical picture, which implied a malignant vascular tumor. In contrast, the cytomorphology of the endothelial cells and the immunohistochemical profile were not suspicious. We worked out subtle histological criteria, which should allow an early detection of such tumors.

摘要

背景

我们研究了2例看似平淡无奇的皮肤血管肉瘤(AS),其临床表现一致,均为鼻子上迅速生长的肿瘤。目前尚不清楚这是原发性皮肤表现还是转移瘤。这两种肿瘤最初在组织学上与良性血管肿瘤有高度重叠。诊断主要基于快速进展的临床病程和分期检查结果。

方法

对细胞角蛋白(AE1/AE3和MNF116)、CD31、ERG、CD34(HPCA1/my10)、D2-40/足板蛋白、LYVE-1、Ki67、PHH3、α平滑肌肌动蛋白(1A4)、MYC、FOS-B、CAMTA-1、TFE-3、WT1、巢蛋白、血管内皮生长因子受体-2(KDR)、血管内皮生长因子受体-3(FLT4)、人疱疹病毒8进行免疫组化染色。还通过荧光原位杂交研究MYC扩增情况。

结果

肿瘤细胞MYC阴性,未显示D2-40/足板蛋白表达。平滑肌肌动蛋白阳性的周细胞在血管周围形成边缘。增殖活性(Ki-67)升高,其中1例仅在后期升高。

讨论

皮肤血管肉瘤可能相当平淡,容易被误诊为良性血管肿瘤。这两例病例临床表现一致,提示为恶性血管肿瘤。相比之下,内皮细胞的细胞形态和免疫组化特征并无可疑之处。我们制定了细微的组织学标准,应有助于早期发现此类肿瘤。

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