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一例罕见的内淋巴囊肿瘤:临床、放射学、病理学及免疫组化结果并文献复习

A Rare Case of Endolymphatic Sac Tumour: Clinical, Radiological, Pathological and Immunohistochemical Findings with Review of Literature.

作者信息

Patel Tarang, Arora Poonam, Meena Virendra Kumar

机构信息

Department of Pathology, Geetanjali Hospital Campus, Geetanjali Medical College & Hospital, B2/G4, Doctors' quarters, NH-8 bypass, Manvakhera, Udaipur, Rajasthan 313002 India.

Department of Radiodiagnosis, Geetanjali Medical College & Hospital, Udaipur, Rajasthan India.

出版信息

Indian J Otolaryngol Head Neck Surg. 2022 Dec;74(Suppl 3):3638-3642. doi: 10.1007/s12070-020-02276-z. Epub 2020 Nov 16.

Abstract

Endolymphatic sac tumour (ELST) is a rare low grade malignant epithelial tumour of the petrous temporal bone, thought to arise from papillary epithelium of the endolymphatic sac. They may occur sporadically or in association with Von-Hippel Lindau disease. ELST is extremely rare neoplasm with benign histopathological appearance and clinically destructive behaviour. Because of the rarity of this tumour, it can easily be confused with other tumours such as paraganglioma, middle ear adenoma, metastatic carcinomas or choroid plexus papilloma. We report here a rare case of ELST with review of literature and discuss the differentiating features of ELST from its mimickers, showing a papillary configuration.

摘要

内淋巴囊肿瘤(ELST)是一种罕见的颞骨岩部低度恶性上皮性肿瘤,被认为起源于内淋巴囊的乳头样上皮。它们可散发出现,或与冯-希佩尔-林道病相关。ELST是一种组织病理学表现为良性但临床行为具有破坏性的极其罕见的肿瘤。由于该肿瘤罕见,它很容易与其他肿瘤混淆,如副神经节瘤、中耳腺瘤、转移性癌或脉络丛乳头状瘤。我们在此报告一例罕见的ELST病例,并复习文献,讨论ELST与其具有乳头状结构的相似肿瘤的鉴别特征。

相似文献

2
Endolymphatic sac tumours.内淋巴囊肿瘤。
Histopathology. 1998 Jul;33(1):2-10. doi: 10.1046/j.1365-2559.1998.00460.x.
3
7
Endolymphatic sac tumours.内淋巴囊肿瘤
J Laryngol Otol. 2002 May;116(5):398-401. doi: 10.1258/0022215021910915.

本文引用的文献

1
4
Three sporadic cases of endolymphatic sac tumor.三例散发性内淋巴囊肿瘤。
Neurol India. 2016 Nov-Dec;64(6):1336-1339. doi: 10.4103/0028-3886.193816.
6
Adenoma of the endolymphatic sac.内淋巴囊腺瘤
J Otolaryngol. 1984 Aug;13(4):213-6.

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