Cystic lymphangioma of nasopharynx in a 54-year-old man - case report. A new histogenetic hypothesis.

IF 1.5
Daniela Vrînceanu, Bogdan Cristian Dorobăţ, Maria Sajin, Carmen Aurelia Mogoantă, Ioana Cristina Oprişcan, Mihaela Cezarina Hîncu, Mădălina Gabriela Georgescu
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引用次数: 0

Abstract

Lymphangiomas are enough rare benign congenital tumors of the lymphatic vessels, frequently encountered during childhood. They are found in the head and neck region, the isolated localization in the nasopharynx is very rare. We present the case of 54-year-old man admitted in the Department of Ear, Nose and Throat (ENT), Emergency University Hospital of Bucharest, Romania, with a nasopharynx tumor certificated by computed tomography (CT) scan with significant bleeding to a previous incisional biopsy temptation rising angiofibroma suspicion. We performed the radical surgical excision of mass by transoral approach. Postoperative bleeding imposed angiography with right internal maxillary artery embolization. Histopathological evaluation showed the diagnosis of lymphangioma. After three years, the patient is without recurrence.

54岁男性鼻咽部囊性淋巴管瘤1例报告。一个新的组织发生假说。
淋巴管瘤是一种罕见的先天性淋巴管良性肿瘤,多见于儿童时期。它们多见于头颈部,孤立地局限于鼻咽部是非常罕见的。我们报告一例54岁的男性患者,在罗马尼亚布加勒斯特急诊大学医院耳鼻喉科(ENT)就诊,其鼻咽肿瘤经计算机断层扫描(CT)证实,先前的切口活检提示明显出血,引起血管纤维瘤的怀疑。我们采用经口入路根治性手术切除肿块。术后出血行右上颌内动脉栓塞血管造影。组织病理学检查诊断为淋巴管瘤。三年后,患者无复发。
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