中耳神经内分泌腺瘤1例报告并文献复习。

IF 0.4 Q4 OTORHINOLARYNGOLOGY
Case Reports in Otolaryngology Pub Date : 2020-12-21 eCollection Date: 2020-01-01 DOI:10.1155/2020/8863188
Luca Bruschini, Rachele Canelli, Christina Cambi, Giacomo Fiacchini, Stefano Berrettini, Francesca Forli
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引用次数: 2

摘要

中耳神经内分泌腺瘤是一种罕见的肿瘤,占耳原发肿瘤的不到2%。在本文中,我们描述了一个40岁的妇女谁发展中耳神经内分泌腺瘤的情况。这种罕见肿瘤的具体治疗策略尚不清楚;现有文献中关于该肿瘤治疗的信息是多种多样的。然而,广泛切除似乎是治疗这种肿瘤的金标准,以避免复发和淋巴结局部转移或远处转移。对于本病例,我们进行了切口活检以确认诊断,此后,我们进行了管道-下壁鼓室成形术。对于像本病例这样的病例,需要仔细的长期临床随访和器械随访,以监测进展并促进患者康复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Middle Ear Neuroendocrine Adenoma: A Case Report and Literature Review.

Middle Ear Neuroendocrine Adenoma: A Case Report and Literature Review.

Middle Ear Neuroendocrine Adenoma: A Case Report and Literature Review.

Middle Ear Neuroendocrine Adenoma: A Case Report and Literature Review.

Neuroendocrine adenomas of the middle ear are rare tumors that represent less than 2% of primary tumors of the ear. In this paper, we describe a case of a 40-year-old woman who developed neuroendocrine adenoma of the middle ear. The specific management strategy for this rare tumor is unclear; information in the available literature on the management of this tumor is varied. However, an extensive demolition seems to be the gold standard treatment for this tumor to avoid recurrence and regional metastases in the lymph node or distant metastases. For the present case, we performed an incisional biopsy to confirm the diagnosis, and thereafter, we performed a canal-wall-down tympanoplasty. For cases like the present one, careful long-term clinical and instrumental follow-up is required to monitor progress and facilitate patient recovery.

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来源期刊
Case Reports in Otolaryngology
Case Reports in Otolaryngology OTORHINOLARYNGOLOGY-
自引率
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发文量
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审稿时长
13 weeks
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