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咬肌上皮样血管肉瘤:一种罕见的临床病理诊断。

Epithelioid angiosarcoma of the masseter muscle: a rare clinicopathological diagnosis.

作者信息

Srivastava Anitya, Nagpal Ruchi, Dhingra Harshi, Baliyan Asif

机构信息

Department of ENT, Dr. Ram Manohar Lohia Institute of medical sciences, Lucknow, Uttar Pradesh, India.

Department of Pathology, Bhaskar Medical College and Hospital Hyderabad, Andhra Pradesh, India.

出版信息

Med Pharm Rep. 2022 Jan;95(1):92-96. doi: 10.15386/mpr-1751. Epub 2022 Jan 31.

Abstract

Epithelioid angiosarcoma (EA) is a subtype of angiosarcoma which is a rare tumor of endothelial origin. Here, we report a case of 15-year-old boy who presented with soft tissue mass lesion in the parotid region mimicking as a benign parotid tumor. Cytology was suggestive of inflammatory swelling. Patient underwent superficial parotidectomy along with the wide excision of the swelling. On histopathology, it was diagnosed as EA. To the best of our knowledge this is the first case report of epithelioid angiosarcoma of the masseter.

摘要

上皮样血管肉瘤(EA)是血管肉瘤的一种亚型,血管肉瘤是一种罕见的起源于内皮的肿瘤。在此,我们报告一例15岁男孩,其腮腺区出现软组织肿块病变,类似良性腮腺肿瘤。细胞学检查提示为炎性肿胀。患者接受了腮腺浅叶切除术及肿块的广泛切除。组织病理学检查确诊为EA。据我们所知,这是首例咬肌上皮样血管肉瘤的病例报告。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/646f/9177093/d36e62798b55/cm-95-92f1.jpg

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