Agrawal Shailesh Ramesh, Joshi Anagha Atul, Dhorje Nikhil, Bradoo Renuka
ENT, Lokmanya Tilak Municipal Medical College and General Hospital, Mumbai, Maharashtra, India.
BMJ Case Rep. 2019 Aug 4;12(8):e230082. doi: 10.1136/bcr-2019-230082.
Respiratory epithelial adenomatoid hamartoma (REAH) is a rare lesion in nasal cavity first reported by Wenig and Heffner in 1995. Most commonly seen in men in third to ninth decade of life. Majority of cases presents as a polypoidal mass in one or both nasal cavities. We experienced such a case of REAH originating from the nasal septum, in posterior aspect, treated by endoscopic approach. It is important to differentiate REAH from other sinonasal pathologies like inverted papilloma and low grade sinonasal adenocarcinoma. Complete surgical resection is the treatment of choice.
呼吸道上皮性腺瘤样错构瘤(REAH)是鼻腔内一种罕见病变,于1995年由韦尼格和赫夫纳首次报道。最常见于30至90岁的男性。大多数病例表现为一个或两个鼻腔内的息肉样肿物。我们遇到了一例起源于鼻中隔后部的REAH病例,采用内镜手术进行治疗。将REAH与其他鼻窦病变如内翻性乳头状瘤和低级别鼻窦腺癌相鉴别很重要。完整手术切除是首选治疗方法。
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