口腔卡西样血管内皮瘤:一种罕见的肿瘤和一个不寻常的位置。

Head and neck pathology Pub Date : 2021-12-01 Epub Date: 2021-03-13 DOI:10.1007/s12105-021-01316-6
Thayná M de Lima Morais, Celeste Sánchez-Romero, Luciano Ribeiro, Daniele S Faé, Francielle S Verner, Oslei P de Almeida, Sibele Nascimento de Aquino
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引用次数: 1

摘要

卡波西样血管内皮瘤是一种少见的中等恶性肿瘤,主要发生于婴幼儿和儿童。累及头部和颈部是罕见的,只有四个病例报告在口腔和口咽。镜下表现为类似卡波西肉瘤的梭形到卵形细胞浸润的血管增生。免疫组化结果:肿瘤CD31、CD34阳性,D2-40阴性。我们在此报告一例罕见的10岁男童口内卡泊样血管内皮瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Kaposiform Hemangioendothelioma of the Oral Cavity: A Rare Tumor with an Unusual Location.

Kaposiform Hemangioendothelioma of the Oral Cavity: A Rare Tumor with an Unusual Location.

Kaposiform hemangioendothelioma is a rare neoplasm with intermediate malignant behavior, mainly affecting infants and children. Involvement head and neck is uncommon, and there are only four cases reported in the oral cavity and oropharynx. Microscopically, it is characterized by a vascular proliferation permeated by spindle-to-ovoid cells resembling Kaposi sarcoma. Immunohistochemically, the tumor is positive for CD31, CD34 and negative for D2-40. Herein we present a rare case of intraoral Kaposiform hemangioendothelioma in a 10-year-old boy.

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