Nefzaoui Safa, Zoghlami Imen, Gharsalli Jihene, Sabehi Emna, Romdhane Nadia, Helal Imen, Chiboub Dorra, Hariga Ines, Mbarek Chiraz
Otorhinolaryngology and Head and Neck Surgery Department, Habib Thameur Hospital, Tunis, Tunisia.
Anatomic Pathology Department, Habib Thameur Hospital, Tunis, Tunisia.
Rare Tumors. 2024 May 14;16:20363613241255567. doi: 10.1177/20363613241255567. eCollection 2024.
Sino-nasal respiratory epithelial adenomatoid hamartomas (REAHs) are rare entity. They are benign tumors with excellent results after complete excision. We report a case of a 57-year-old male with a history of endoscopic surgery for right nasal polyps 20 years ago. The patient presented nasal obstruction that persisted for 10 years without anosmia nor epistaxis. Nasal endoscopy found a tissular mass filling the right nasal cavity extending to the nasopharynx. CT scan and MRI demonstrated soft tissue opacification of the right maxillary sinus and the homolateral anterior ethmoid cells with extension to the nasal cavity. The suspected diagnosis on imaging was an Inverted papilloma with a wide implantation base on the posterior part of the nasal septum. No endocranial or orbital extension was noted. The patient underwent endoscopic sinus surgery with complete extirpation of the tumor and a right ethmoidectomy. Histopathological assessment showed features consistent with REAH. No recurrence was noted at 1 year follow-up.
鼻窦呼吸上皮腺样错构瘤(REAHs)是一种罕见的疾病。它们是良性肿瘤,完整切除后效果良好。我们报告一例57岁男性,20年前有右侧鼻息肉内镜手术史。患者出现鼻塞10年,无嗅觉减退或鼻出血。鼻内镜检查发现一个组织块充满右侧鼻腔并延伸至鼻咽部。CT扫描和MRI显示右侧上颌窦及同侧前筛窦软组织混浊并延伸至鼻腔。影像学上疑似诊断为内翻性乳头状瘤,在鼻中隔后部有一个宽基底植入。未发现颅内或眶内侵犯。患者接受了内镜鼻窦手术,肿瘤完整切除并进行了右侧筛窦切除术。组织病理学评估显示符合REAH的特征。随访1年未发现复发。
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