Yoruk Ozgur, Erdem Havva, Mutlu Vahit, Erdogan Fazli, Altas Enver, Kantarci Mecit
Department of Otolaryngology, Medical Faculty, Ataturk University, Erzurum, Turkey.
Auris Nasus Larynx. 2008 Mar;35(1):157-9. doi: 10.1016/j.anl.2007.05.005. Epub 2007 Sep 19.
Epithelioid hemangioendothelioma (EH) is a seldom tumor of vascular origin, which occurs at sites such as liver, lung or soft tissues, and has a highly unpredictable malignant potential and clinical course. We submitted a case with epithelioid hemangioendothelioma of submandibular gland. The patient was a 44-year-old woman who presented with left submandibular painly mass. Fine needle aspiration showed a mixed lymphoid population. Contrast enhanced Computerize Tomography (CT) scan revealed that to be a well-circumscribed and including microcalcification in centre 2.5 cm x 2.0 cm mass in diameter without evidence of bony invasion. Submandibular gland was excised. The pathological result was interpretated as epithelioid hemangioendothelioma of the submandibular gland. The patient was seen regularly for recurrence.
上皮样血管内皮瘤(EH)是一种罕见的血管源性肿瘤,发生于肝脏、肺或软组织等部位,具有高度不可预测的恶性潜能和临床病程。我们报告一例下颌下腺上皮样血管内皮瘤病例。患者为44岁女性,表现为左侧下颌下疼痛性肿块。细针穿刺显示为混合淋巴细胞群。增强计算机断层扫描(CT)显示为一个边界清晰、直径2.5 cm×2.0 cm、中心有微钙化的肿块,无骨质侵犯证据。切除下颌下腺。病理结果诊断为下颌下腺上皮样血管内皮瘤。定期观察患者有无复发情况。