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以溢泪为首发症状的鼻腔神经内分泌癌:一例报告

Neuroendocrine carcinoma of the nasal cavity with epiphora as the first symptom: A case report.

作者信息

Wu Weiqi, Gan Puying, Xu Qihua, Wang Yaohua, Liao Hongfei

机构信息

Department of Ocular Oncology and Ocular Trauma, Affiliated Eye Hospital of Nanchang University, Jiangxi Research Institute of Ophthalmology and Visual Sciences, Key Laboratory of Ophthalmology of Jiangxi province.

Medical Department of Graduate School, Nanchang University, Nanchang, Jiangxi, China.

出版信息

Medicine (Baltimore). 2020 Dec 4;99(49):e23502. doi: 10.1097/MD.0000000000023502.

DOI:10.1097/MD.0000000000023502
PMID:33285758
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7717802/
Abstract

RATIONALE

Neuroendocrine carcinomas (NECs) are rare malignancies that originate from the hormone-producing cells of the neuroendocrine system. They can grow in most organs of the body but are commonly found in the gastrointestinal and respiratory tracts. The nasal cavity is a rare site for NECs.

PATIENT CONCERNS

We report a case of NECs in a 45-year-old woman who presented with epiphora in the right eye for a year owing to an unknown reason.

DIAGNOSES

The diagnosis was initially confirmed via histological and immunohistochemical assays. Postoperatively, computed tomography of the neck revealed C4 vertebral bone metastasis.

INTERVENTIONS

The tumor was endoscopically removed from the right eye. The patient received a full course of adjuvant polychemotherapy.

OUTCOMES

Six months after diagnosis, the patient died due to bone metastasis.

LESSONS

Diagnosing nasal neuroendocrine carcinoma is clinically challenging. It must be distinguished from other orbital masses, such as chronic dacryocystitis or nasal polyps. The treatment should be further investigated for this rare malignancy in near future.

摘要

原理

神经内分泌癌(NECs)是起源于神经内分泌系统激素产生细胞的罕见恶性肿瘤。它们可在身体的大多数器官中生长,但常见于胃肠道和呼吸道。鼻腔是神经内分泌癌的罕见发病部位。

患者情况

我们报告一例45岁女性神经内分泌癌病例,该患者右眼流泪一年,原因不明。

诊断

最初通过组织学和免疫组化检测确诊。术后,颈部计算机断层扫描显示C4椎体骨转移。

干预措施

通过内镜从右眼切除肿瘤。患者接受了全程辅助多药化疗。

结果

诊断后六个月,患者因骨转移死亡。

经验教训

诊断鼻腔神经内分泌癌在临床上具有挑战性。它必须与其他眼眶肿物,如慢性泪囊炎或鼻息肉相鉴别。对于这种罕见恶性肿瘤的治疗,在不久的将来应进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ce4/7717802/5da852c56c7b/medi-99-e23502-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ce4/7717802/9ff72d742321/medi-99-e23502-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ce4/7717802/ddc9dbb87488/medi-99-e23502-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ce4/7717802/77bd1fb62eb2/medi-99-e23502-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ce4/7717802/5da852c56c7b/medi-99-e23502-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ce4/7717802/9ff72d742321/medi-99-e23502-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ce4/7717802/ddc9dbb87488/medi-99-e23502-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ce4/7717802/77bd1fb62eb2/medi-99-e23502-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ce4/7717802/5da852c56c7b/medi-99-e23502-g004.jpg

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本文引用的文献

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Large-cell neuroendocrine carcinoma of nasal cavity and paranasal sinuses after successful curative therapy: a case report and literature review.鼻腔和鼻窦大细胞神经内分泌癌根治性治疗成功后:一例报告及文献复习
Onco Targets Ther. 2019 Apr 17;12:2975-2980. doi: 10.2147/OTT.S195052. eCollection 2019.
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Large cell neuroendocrine carcinoma of the nasal cavity: an extremely rare and new distinct entity.鼻腔大细胞神经内分泌癌:一种极其罕见的新型独特实体。
Pan Afr Med J. 2018 Jun 29;30:188. doi: 10.11604/pamj.2018.30.188.14992. eCollection 2018.
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[Eight Cases of Small Cell Neuroendocrine Carcinoma of the Head and Neck].
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A review of nasal, paranasal, and skull base tumors invading the orbit.鼻腔、副鼻窦和颅底肿瘤侵犯眼眶的综述。
Surv Ophthalmol. 2018 May-Jun;63(3):389-405. doi: 10.1016/j.survophthal.2017.07.001. Epub 2017 Jul 22.
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Update from the 4th Edition of the World Health Organization Classification of Head and Neck Tumours: What is New in the 2017 WHO Blue Book for Tumours of the Hypopharynx, Larynx, Trachea and Parapharyngeal Space.世界卫生组织头颈部肿瘤分类第4版更新内容:2017年世界卫生组织下咽、喉、气管及咽旁间隙肿瘤蓝皮书有哪些新内容。
Head Neck Pathol. 2017 Mar;11(1):23-32. doi: 10.1007/s12105-017-0788-z. Epub 2017 Feb 28.
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Am J Surg Pathol. 2017 Apr;41(4):525-534. doi: 10.1097/PAS.0000000000000784.
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