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分泌促卵泡生成素的垂体神经内分泌肿瘤作为卵巢过度刺激综合征的一个病因

FSH-producing pituitary neuroendocrine tumor as a cause of ovarian hyperstimulation syndrome.

作者信息

Kitamura Takuya, Nanba Kazutaka, Doi Kento, Kishimoto Naoya, Abiko Kaoru, Kuwahara Ryo, Moriyoshi Koki, Inoshita Naoko, Tagami Tetsuya

机构信息

Department of Endocrinology and Metabolism, National Hospital Organization Kyoto Medical Center, Kyoto, Japan.

Department of Endocrinology, Metabolism, and Hypertension Research, Clinical Research Institute, National Hospital Organization Kyoto Medical Center, Kyoto, Japan.

出版信息

Endocrinol Diabetes Metab Case Rep. 2024 Feb 28;2024(1). doi: 10.1530/EDM-23-0119. Print 2024 Jan 1.

Abstract

SUMMARY

Functioning gonadotroph tumors are rare neoplasms that can cause ovarian hyperstimulation syndrome (OHSS) in women of reproductive age. Here, we present a case of a follicle-stimulating hormone (FSH)-producing pituitary neuroendocrine tumor (PitNET) with irregular menstrual cycles and OHSS in a Japanese woman. A 34-year-old woman with bilateral multi-cystic ovarian mass was referred to our hospital for ovarian surgery. The imaging feature of magnetic resonance imaging (MRI) of the ovary and elevated estradiol levels with normal FSH and low luteinizing hormone (LH) levels led us to suspect the presence of a functioning gonadotroph PitNET. MRI revealed a 19-mm pituitary tumor, and increased tracer uptake was observed in the pituitary lesion on 111In-pentetreotide scintigraphy. Transsphenoidal tumor resection resulted in the resolution of the ovarian enlargement, normalization of her menstrual cycles, and spontaneous pregnancy. Immunohistochemistry (IHC) of the resected tumor for pituitary transcription factors, including steroidogenesis factor 1 (SF1) and estrogen receptor alpha, demonstrated positive immunoreactivity, whereas IHC for pituitary-specific positive transcription factor 1 was negative, suggesting that the tumor belonged to the SF1 lineage of PitNETs (gonadotroph tumor). The tumor cells showed positive expression of FSHβ, while LHβ was mostly negative. Consistent with the high pituitary tumor uptake observed on 111In-pentetreotide scintigraphy, the pituitary tumor showed positive expression of somatostatin receptor 2A. Detailed clinical and histological evaluations will provide useful information to understand these rare functioning gonadotroph tumors better.

LEARNING POINTS

Functioning gonadotroph tumors are very rare neuroendocrine tumors of pituitary origin. Women of reproductive age presenting with bilateral multi-cystic ovarian enlargement, irregular menstrual cycles, and hyperestrogenemia under unsuppressed follicle-stimulating hormone (FSH) levels should be evaluated for FSH-producing tumor. Raising awareness of OHSS due to functioning gonadotroph tumors is crucial to prevent unnecessary ovarian surgery. Comprehensive histological analysis may provide useful information to better understand the characteristics of functioning gonadotroph tumors.

摘要

摘要

功能性促性腺激素瘤是一种罕见的肿瘤,可导致育龄期女性发生卵巢过度刺激综合征(OHSS)。在此,我们报告一例日本女性患有分泌促卵泡生成素(FSH)的垂体神经内分泌肿瘤(PitNET),伴有月经周期不规律和OHSS。一名34岁双侧多囊卵巢肿块的女性因卵巢手术被转诊至我院。卵巢磁共振成像(MRI)的影像学特征以及雌二醇水平升高而FSH水平正常、黄体生成素(LH)水平降低,使我们怀疑存在功能性促性腺激素PitNET。MRI显示垂体有一个19毫米的肿瘤,在111铟-喷替酸奥曲肽闪烁扫描中垂体病变处观察到放射性示踪剂摄取增加。经蝶窦肿瘤切除术使卵巢肿大消退、月经周期恢复正常并自然受孕。对切除肿瘤进行的垂体转录因子免疫组织化学(IHC)检测,包括类固醇生成因子1(SF1)和雌激素受体α,显示免疫反应阳性,而垂体特异性阳性转录因子1的IHC检测为阴性,提示该肿瘤属于PitNETs的SF1谱系(促性腺激素瘤)。肿瘤细胞FSHβ表达阳性,而LHβ大多为阴性。与111铟-喷替酸奥曲肽闪烁扫描中观察到的垂体肿瘤高摄取一致,垂体肿瘤生长抑素受体2A表达阳性。详细的临床和组织学评估将为更好地了解这些罕见的功能性促性腺激素瘤提供有用信息。

学习要点

功能性促性腺激素瘤是非常罕见的起源于垂体的神经内分泌肿瘤。对于育龄期女性出现双侧多囊卵巢肿大、月经周期不规律以及在未受抑制的促卵泡生成素(FSH)水平下出现高雌激素血症的情况,应评估是否存在分泌FSH的肿瘤。提高对功能性促性腺激素瘤导致OHSS的认识对于预防不必要的卵巢手术至关重要。全面的组织学分析可能为更好地了解功能性促性腺激素瘤的特征提供有用信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a8a/10959052/6b4b37109723/EDM23-0119fig1.jpg

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