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罕见的原发性输卵管2级神经内分泌肿瘤:一例病例报告并文献复习

Rare Primary Fallopian Tube Grade 2 Neuroendocrine Tumor: A Case Report With Review of Literature.

作者信息

Kwon Grace J, Jorgensen Jennifer R, Vedere Tarunya R, Sanders Melinda, Nam Gahie

出版信息

Int J Gynecol Pathol. 2023 Nov 1;42(6):632-639. doi: 10.1097/PGP.0000000000000944. Epub 2023 Jan 25.

Abstract

Neuroendocrine neoplasms commonly arise from the gastrointestinal tract and lungs. Less commonly, they may occur in the gynecologic tract, typically within the ovary of a mature cystic teratoma. Primary neuroendocrine neoplasms of the fallopian tube are exceptionally rare and only a total of 11 cases have been reported in the literature. We describe the first case to our knowledge of a primary grade 2 neuroendocrine tumor of the fallopian tube in a 47-yr-old female. In this report, we describe the case's unique presentation, review the published literature on primary neuroendocrine neoplasms of the fallopian tube, discuss the treatment options, and speculate on their origin and histogenesis.

摘要

神经内分泌肿瘤通常起源于胃肠道和肺部。较少见的情况下,它们可能发生在生殖道,通常在成熟囊性畸胎瘤的卵巢内。输卵管原发性神经内分泌肿瘤极为罕见,文献中仅报道了11例。我们报道了据我们所知的首例47岁女性原发性输卵管2级神经内分泌肿瘤病例。在本报告中,我们描述了该病例的独特表现,回顾了关于输卵管原发性神经内分泌肿瘤的已发表文献,讨论了治疗方案,并推测了其起源和组织发生。

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