Angiofibrolipoma in the Head and Neck Region: A Case Report and Literature Review.

Ahmad Alkheder, Adel Azar, Ahmad Mustafa
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Abstract

Angiofibrolipomas are rare, benign soft tissue tumors composed of mature fat cells, blood vessels, and fibrous connective tissue. Typically occurring in subcutaneous locations, this case report presents a unique instance of an angiofibrolipoma arising in the pharynx. According to our review of the literature, it is the second reported case in the pharynx and the sixth in the head and neck region. A 58-year-old woman presented with a 1 year history of globus sensation and an incidentally-discovered extra-oral polyp. Endoscopic examination revealed the polyp originating from the upper esophagus and extending into the pharynx. Magnetic resonance imaging confirmed the nature and extent of the lesion. The polyp was successfully removed via endoscopic resection, and histopathological analysis confirmed the diagnosis of angiofibrolipoma. This case highlights the rarity of pharyngeal angiofibrolipomas and underscores the importance of endoscopic evaluation for patients presenting with ambiguous pharyngeal symptoms. While surgical resection is generally recommended for such tumors, endoscopic removal can be a safe and effective option for smaller pedunculated lesions.

头颈部血管纤维脂肪瘤:病例报告和文献综述。
血管纤维脂肪瘤是一种罕见的良性软组织肿瘤,由成熟的脂肪细胞、血管和纤维结缔组织组成。血管纤维脂肪瘤通常发生在皮下部位,本病例报告了一例发生在咽部的血管纤维脂肪瘤。根据我们查阅的文献,这是第二例咽部血管纤维脂肪瘤病例,也是第六例头颈部血管纤维脂肪瘤病例。一名 58 岁的女性患者有 1 年的咽喉痛病史,偶然发现了口外息肉。内窥镜检查发现息肉来自食管上段并延伸至咽部。磁共振成像证实了病变的性质和范围。通过内镜切除术成功摘除了息肉,组织病理分析证实了血管纤维脂肪瘤的诊断。该病例凸显了咽部血管纤维脂肪瘤的罕见性,并强调了对出现咽部症状不明确的患者进行内窥镜评估的重要性。虽然一般建议对此类肿瘤进行手术切除,但对于较小的有蒂病变,内窥镜切除也是一种安全有效的选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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