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一名患有纯原发性卵巢神经内分泌肿瘤的年轻伊朗女性:病例报告

A Young Iranian Woman with Pure Primary Ovarian Neuroendocrine Tumor: A Case Report.

作者信息

Samiee-Rad Fatemeh, Ghaebi Mahdi, Bajelan Arezoo

机构信息

Clinical Research Development Unit, Kosar Hospital, Qazvin University of Medical Sciences, Qazvin, Iran.

出版信息

Iran J Pathol. 2022 Summer;17(3):371-375. doi: 10.30699/IJP.2022.542788.2766. Epub 2021 Aug 14.

DOI:10.30699/IJP.2022.542788.2766
PMID:36247498
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9508533/
Abstract

Pure ovarian neuroendocrine tumors are very rare. Herein, we present a young Iranian woman with a pure primary ovarian neuroendocrine tumor. A 26-year-old female presented with chronic abdominal pain and progressive constipation and was referred to the emergency room. Imaging findings confirmed a mass in the right adnexa. Following the resectional surgery of the ovarian mass, histopathological and immunohistochemistry results disclosed a mixed type of primary ovarian neuroendocrine tumor. The patient did not experience tumor recurrence afterward. Due to the rarity and low prevalence of primary pure ovarian neuroendocrine tumors, the histopathologic diagnosis should be confirmed by an immunohistochemistry study.

摘要

纯原发性卵巢神经内分泌肿瘤非常罕见。在此,我们报告一位患有纯原发性卵巢神经内分泌肿瘤的年轻伊朗女性。一名26岁女性因慢性腹痛和进行性便秘就诊于急诊室。影像学检查发现右侧附件有一肿块。在对卵巢肿块进行切除手术后,组织病理学和免疫组化结果显示为混合型原发性卵巢神经内分泌肿瘤。该患者术后未出现肿瘤复发。由于原发性纯卵巢神经内分泌肿瘤罕见且发病率低,组织病理学诊断应通过免疫组化研究来证实。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02e5/9508533/dce72f93ef49/ijp-17-371-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02e5/9508533/7abfa3661dd5/ijp-17-371-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02e5/9508533/4f48b020d4dd/ijp-17-371-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02e5/9508533/28ac6abb9a09/ijp-17-371-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02e5/9508533/dce72f93ef49/ijp-17-371-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02e5/9508533/7abfa3661dd5/ijp-17-371-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02e5/9508533/4f48b020d4dd/ijp-17-371-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02e5/9508533/28ac6abb9a09/ijp-17-371-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02e5/9508533/dce72f93ef49/ijp-17-371-g004.jpg

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本文引用的文献

1
Global burden of neuroendocrine tumors and changing incidence in Kentucky.肯塔基州神经内分泌肿瘤的全球负担及发病率变化
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Peptide YY producing strumal carcinoid tumor of the ovary in a postmenopausal woman: a rare cause of chronic constipation.
绝经后女性卵巢产生肽YY的甲状腺样类癌肿瘤:慢性便秘的罕见病因
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Neuroendocrine Neoplasms: Dichotomy, Origin and Classifications.神经内分泌肿瘤:二分法、起源与分类
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Frequency of carcinoid syndrome at neuroendocrine tumour diagnosis: a population-based study.神经内分泌肿瘤诊断时类癌综合征的发生率:一项基于人群的研究。
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Neuroendocrine Tumors of the Female Reproductive Tract: A Literature Review.女性生殖道神经内分泌肿瘤:文献综述
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Neuroendocrine tumours of the female genital tract: a case-based imaging review with pathological correlation.女性生殖道神经内分泌肿瘤:基于病例的影像学与病理学相关性综述。
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10
Ovarian strumal carcinoid producing peptide YY associated with severe constipation: a case report and review of the literature.产生肽YY的卵巢甲状腺肿类癌伴严重便秘:一例报告并文献复习
Int J Gynecol Pathol. 2015 Jan;34(1):30-5. doi: 10.1097/PGP.0000000000000117.