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Hamartomatous Polyp of the Nasopharynx: A Rare Case Report.鼻咽部错构瘤性息肉:1例罕见病例报告
Indian J Otolaryngol Head Neck Surg. 2019 Nov;71(Suppl 3):1727-1729. doi: 10.1007/s12070-017-1077-6. Epub 2017 Feb 6.
2
Bilateral respiratory epithelial adenomatoid hamartomas originating from the anterior olfactory clefts.起源于前嗅裂的双侧呼吸道上皮腺样错构瘤。
Proc (Bayl Univ Med Cent). 2017 Apr;30(2):221-223. doi: 10.1080/08998280.2017.11929594.
3
Huge Respiratory Epithelial Adenomatoid Hamartoma Originating from the Inferior Nasal Turbinate: A Case Report.起源于下鼻甲的巨大呼吸道上皮腺样错构瘤:一例报告
Indian J Otolaryngol Head Neck Surg. 2016 Mar;68(1):100-3. doi: 10.1007/s12070-015-0849-0. Epub 2015 Apr 21.
4
Predictors of respiratory epithelial adenomatoid hamartomas of the olfactory clefts in patients with nasal polyposis.鼻息肉患者嗅裂呼吸上皮腺样错构瘤的预测因素。
Laryngoscope. 2014 Nov;124(11):2461-5. doi: 10.1002/lary.24778. Epub 2014 Jun 13.
5
Respiratory epithelial adenomatoid hamartoma: a poorly recognized entity with mast cell recruitment and frequently associated with nasal polyposis.呼吸上皮腺瘤样错构瘤:一种认识不足的实体,伴有肥大细胞募集,常与鼻息肉相关。
Am J Surg Pathol. 2013 Nov;37(11):1678-85. doi: 10.1097/PAS.0000000000000092.
6
Sinonasal respiratory epithelial adenomatoid hamartomas: series of 51 cases and literature review.鼻腔呼吸上皮腺样错构瘤:51 例系列病例及文献复习。
Am J Rhinol Allergy. 2013 Jul-Aug;27(4):322-8. doi: 10.2500/ajra.2013.27.3905.
7
Respiratory epithelial adenomatoid hamartoma originating from nasal septum.起源于鼻中隔的呼吸上皮腺瘤样错构瘤。
Clin Exp Otorhinolaryngol. 2013 Mar;6(1):45-7. doi: 10.3342/ceo.2013.6.1.45. Epub 2011 Nov 29.
8
CT findings of sinonasal respiratory epithelial adenomatoid hamartoma: a closer look at the olfactory clefts.鼻窦呼吸上皮腺瘤样错构瘤的 CT 表现:嗅裂的深入观察。
AJNR Am J Neuroradiol. 2013 May;34(5):1086-90. doi: 10.3174/ajnr.A3345. Epub 2012 Nov 22.
9
Hamartoma of the head and neck.
Indian J Otolaryngol Head Neck Surg. 1999 Oct;51(4):76-8. doi: 10.1007/BF03022724.
10
Respiratory epithelial adenomatoid hamartomas.呼吸上皮腺样错构瘤。
Laryngoscope. 2011 Dec;121(12):2706-9. doi: 10.1002/lary.22399. Epub 2011 Oct 17.

嗅裂区呼吸道上皮腺样错构瘤(REAH):常被双侧鼻息肉掩盖。

Respiratory Epithelial Adenomatoid Hamartoma (REAH) in the Olfactory Cleft: Often Masked by Bilateral Nasal Polyps.

作者信息

Shanbag Raghunath, Patil Prakash, Rani S Hephzibah, Kulkarni Sughosh

机构信息

1Department of ENT, SDM College of Medical Sciences and Hospital, Manjushree Nagar, Dharwad, Karnataka 580009 India.

2SDM Biomedical Research Center, SDM College of Medical Sciences and Hospital Campus, Manjushree Nagar, Dharwad, Karnataka 580009 India.

出版信息

Indian J Otolaryngol Head Neck Surg. 2019 Nov;71(Suppl 3):2121-2126. doi: 10.1007/s12070-018-1562-6.

DOI:10.1007/s12070-018-1562-6
PMID:31763306
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6848398/
Abstract

Respiratory epithelial adenomatoid hamartoma (REAH) is a distinct non-neoplastic entity originating from anterior olfactory cleft in the nasal cavity, often going unnoticed. Clinically, REAH presents as unilateral or bilateral nasal polyps. Our aim is to expand the understanding of bilateral REAH associated with nasal polyposis with respect to clinical, radiological and histopathological features for better clinical outcomes. Our analysis includes patients presenting as bilateral nasal polyps, whose CT-PNS showed opacity in olfactory clefts. During endoscopic sinus surgery, the lesions in the olfactory cleft (medial-to-middle turbinate) were identified and the specimens from olfactory cleft and ethmoid sinus cavity were subjected separately to histopathological analysis. Six patients (average age 50 years, 83% male) of bilateral REAH with nasal obstruction of > 3 years were analysed. On nasal endoscopy, the polypoid masses in the olfactory cleft and in the ethmoids did not show any gross differences. However, polypoidal masses from the olfactory cleft bled more during biopsy and excision. Histopathological study of these masses revealed the closely arranged round to oval glands (with few dilated glands) lined by ciliated columnar epithelium in mildly edematous stroma, confirming the presence of REAH. REAH is an often overlooked lesion in the nasal cavity, arising from olfactory cleft. The presence of nasal polyposis obscures this lesion, resulting in under diagnosis. The prompt identification with high index of suspicion by the otorhinolaryngologists helps in accurate histopathological diagnosis thereby improving clinical outcomes.

摘要

呼吸道上皮腺样错构瘤(REAH)是一种起源于鼻腔前嗅裂的独特的非肿瘤性病变,常未被注意到。临床上,REAH表现为单侧或双侧鼻息肉。我们的目的是在临床、影像学和组织病理学特征方面,扩大对与鼻息肉相关的双侧REAH的认识,以获得更好的临床结果。我们的分析包括表现为双侧鼻息肉且CT-PNS显示嗅裂混浊的患者。在内镜鼻窦手术中,识别嗅裂(中鼻甲内侧)的病变,并将来自嗅裂和筛窦腔的标本分别进行组织病理学分析。对6例双侧REAH且鼻塞超过3年的患者(平均年龄50岁,83%为男性)进行了分析。鼻内镜检查时,嗅裂和筛窦内的息肉样肿物在外观上无明显差异。然而,嗅裂处的息肉样肿物在活检和切除时出血更多。对这些肿物的组织病理学研究显示,在轻度水肿的间质中,有紧密排列的圆形至椭圆形腺体(少数腺体扩张),内衬纤毛柱状上皮,证实为REAH。REAH是鼻腔中常被忽视的病变,起源于嗅裂。鼻息肉的存在掩盖了这种病变,导致诊断不足。耳鼻喉科医生高度怀疑并及时识别有助于准确的组织病理学诊断,从而改善临床结果。