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婴儿期卵巢性索间质肿瘤伴同性性早熟 1 例报告及文献复习

A rare case of Ovarian Juvenile Granulosa Cell Tumor in an Infant with Isosexual Pseudo Puberty and a Revision of Literature.

机构信息

Quisisana Hospital, Ferrara.

Pediatric Endocrinology Department, Hamad Medical Corporation.

出版信息

Acta Biomed. 2021 Sep 2;92(4):e2021319. doi: 10.23750/abm.v92i4.11572.

DOI:10.23750/abm.v92i4.11572
PMID:34487069
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8477099/
Abstract

Juvenile ovarian granulosa cell tumors (JGCTs) are described infrequently in pediatrics, and their finding in infants is exceptional. We highlight the presenting symptoms, radiologic images, operative management, and histopathologic findings of a 9-month-old female with isosexual pseudopuberty. An updated revision of literature in infants below the age of 12 months is also reported.

摘要

婴儿型卵巢颗粒细胞瘤(JGCT)在儿科中罕见报道,其在婴儿中的发现更是罕见。我们重点介绍了一例 9 月龄女性出现两性假性性早熟的临床表现、影像学表现、手术治疗及组织病理学检查结果。同时还对 12 月龄以下婴儿的相关文献进行了更新综述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adaa/8477099/a510647e0398/ACTA-92-319-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adaa/8477099/f24b4c4ee5b2/ACTA-92-319-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adaa/8477099/90b9d2e4b027/ACTA-92-319-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adaa/8477099/f47629632de1/ACTA-92-319-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adaa/8477099/7a573fccf850/ACTA-92-319-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adaa/8477099/a510647e0398/ACTA-92-319-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adaa/8477099/f24b4c4ee5b2/ACTA-92-319-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adaa/8477099/90b9d2e4b027/ACTA-92-319-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adaa/8477099/f47629632de1/ACTA-92-319-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adaa/8477099/7a573fccf850/ACTA-92-319-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adaa/8477099/a510647e0398/ACTA-92-319-g005.jpg

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A rare case of Ovarian Juvenile Granulosa Cell Tumor in an Infant with Isosexual Pseudo Puberty and a Revision of Literature.婴儿期卵巢性索间质肿瘤伴同性性早熟 1 例报告及文献复习
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J Immunother Precis Oncol. 2024 Aug 1;7(4):263-271. doi: 10.36401/JIPO-23-40. eCollection 2024 Nov.
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Clinical utility of anti-Müllerian hormone in female children and adolescents.抗苗勒管激素在女童及青少年中的临床应用
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本文引用的文献

1
[Granulosa cell ovarian tumor: precocious puberty in infant less than 1 year of age. Case report].[颗粒细胞卵巢肿瘤:1岁以下婴儿性早熟。病例报告]
Rev Chil Pediatr. 2017 Dec;88(6):792-797. doi: 10.4067/S0370-41062017000600792.
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A rare case of ovarian juvenile granulosa cell tumor without precocious pseudopuberty in an 11-month-old infant.一名11个月大婴儿患罕见的无性早熟假性青春期的卵巢幼年型颗粒细胞瘤病例。
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Juvenile granulosa cell ovarian tumor: a case report and review of literature.
青少年颗粒细胞卵巢肿瘤:一例病例报告及文献复习
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Ovarian juvenile granulosa cell tumors in infants.婴儿卵巢幼年型颗粒细胞瘤
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Granulosa cell tumor of the ovary: tumor review.卵巢颗粒细胞瘤:肿瘤综述
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Granulosa cell tumor of the ovary.卵巢颗粒细胞瘤
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Ovarian granulosa cell tumors in childhood.儿童卵巢颗粒细胞瘤
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[A case of a granulosa-cell tumor in a 10-month-old nursing infant].[一例10个月大哺乳期婴儿的颗粒细胞瘤病例]
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Precocious pseudopuberty due to a granulosa cell tumour in a seven-month-old female.
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Juvenile granulosa cell tumor of the ovary in infants: a clinicopathologic study of three cases and review of the literature.
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