Oral & Maxillofacial surgery, Krishna Institute of Medical Sciences Deemed University, Karad, Maharashtra, India
Calcutta Institute of Maxillofacial Surgery and Research, Kolkata, India.
BMJ Case Rep. 2020 Jul 5;13(7):e234985. doi: 10.1136/bcr-2020-234985.
Sinonasal inverted schneiderian papilloma (ISP) is a rare tumour, which almost exclusively arises from the mucosa lining, the nasal cavity and the paranasal sinuses. The tumour in its early stages presents as an asymptomatic mass, which may be discovered during routine examination. Large lesions usually measure a few millimetres to centimetres in size and show symptoms such as nasal blockade, recurrent sinusitis, postnasal drip, anosmia, epistaxis, facial pain and headache. Lesion presenting as a large oral mass is extremely rare and may cause diagnostic dilemma, resulting in misdiagnosis. This report describes a rare case of ISP presenting as large intraoral lesion, with wide area of facial skeletal involvement. Diagnosis and management of the pathology has also been highlighted.
鼻腔鼻窦内翻性乳头状瘤(ISP)是一种罕见的肿瘤,几乎完全来源于鼻腔和鼻窦的黏膜内层。肿瘤在早期阶段表现为无症状的肿块,可能在常规检查中发现。大的病变通常大小为数毫米至数厘米,并出现鼻塞、复发性鼻窦炎、后鼻滴注、嗅觉丧失、鼻出血、面部疼痛和头痛等症状。表现为口腔内大肿块的病变极为罕见,可能导致诊断上的困境,导致误诊。本报告描述了一例罕见的 ISP 病例,表现为口腔内大的病变,广泛累及面部骨骼。还强调了对该病变的诊断和处理。