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揭示罕见病例:罕见生殖细胞肿瘤病例系列

Unveiling the Uncommon: A Case Series on Rare Germ Cell Tumors.

作者信息

Chakrabarti Asmita, Kumari Shailaja, Maiti Moumita, DAS Chhanda, Barui Gopinath

机构信息

Nil Ratan Sircar Medical College and Hospital.

出版信息

Curr Health Sci J. 2024 Oct-Dec;50(5):599-606. doi: 10.12865/CHSJ.50.04.14. Epub 2024 Dec 31.

DOI:10.12865/CHSJ.50.04.14
PMID:40143878
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11936066/
Abstract

INTRODUCTION

Germ cell tumors (GCTs) are heterogeneous group of neoplasms that arise from primordial germ cells and can occur in various locations, most commonly in the ovaries and testes but can also be found in extra-gonadal sites like retroperitoneum due to developmental errors. These tumors are relatively rare but clinically significant due to their potential for malignancy and association with developmental anomalies.

CASE PRESENTATION

This case series presents four rare and unusual cases of germ cell tumors encountered in both paediatric and adult patients, each with distinctive clinical, radiological, and histopathological features. These cases are unique in their clinical presentation and histomorphological findings, reflecting the diverse spectrum of GCTs across different age groups.

CONCLUSION

These cases underscore the complexity of diagnosis, the role of radiological and histopathological examinations, and the varied management strategies for rare conditions like gonadoblastoma, dysgerminoma, struma ovarii, and fetus-in-fetu.

摘要

引言

生殖细胞肿瘤(GCTs)是一组异质性肿瘤,起源于原始生殖细胞,可发生于多个部位,最常见于卵巢和睾丸,但也可因发育异常而在性腺外部位如腹膜后发现。这些肿瘤相对罕见,但因其潜在的恶性程度以及与发育异常的关联而具有临床意义。

病例报告

本病例系列展示了在儿科和成年患者中遇到的4例罕见且不寻常的生殖细胞肿瘤病例,每例都具有独特的临床、放射学和组织病理学特征。这些病例在临床表现和组织形态学发现方面具有独特性,反映了不同年龄组GCTs的多样谱。

结论

这些病例强调了诊断的复杂性、放射学和组织病理学检查的作用,以及对于诸如性腺母细胞瘤、无性细胞瘤、卵巢甲状腺肿和胎中胎等罕见病症的不同管理策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6dd/11936066/65e8a562c0e2/CHSJ-50-04-599-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6dd/11936066/0038ccec84b4/CHSJ-50-04-599-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6dd/11936066/4e6721f86efe/CHSJ-50-04-599-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6dd/11936066/85fa5f57a048/CHSJ-50-04-599-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6dd/11936066/65e8a562c0e2/CHSJ-50-04-599-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6dd/11936066/0038ccec84b4/CHSJ-50-04-599-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6dd/11936066/4e6721f86efe/CHSJ-50-04-599-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6dd/11936066/85fa5f57a048/CHSJ-50-04-599-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6dd/11936066/65e8a562c0e2/CHSJ-50-04-599-fig4.jpg

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本文引用的文献

1
Diagnosis and Management of Dysgerminomas with a Brief Summary of Primitive Germ Cell Tumors.无性细胞瘤的诊断与管理及原始生殖细胞肿瘤简要概述
Diagnostics (Basel). 2022 Dec 9;12(12):3105. doi: 10.3390/diagnostics12123105.
2
Gonadoblastoma: origin and outcome.精原细胞瘤:起源与结局。
Hum Pathol. 2020 Jun;100:47-53. doi: 10.1016/j.humpath.2019.11.005. Epub 2019 Dec 2.
3
Extragonadal germ cell tumors: Not just a matter of location. A review about clinical, molecular and pathological features.性腺外生殖细胞肿瘤:不只是位置的问题。一篇关于临床、分子和病理特征的综述。
Cancer Med. 2019 Nov;8(16):6832-6840. doi: 10.1002/cam4.2195. Epub 2019 Sep 30.
4
Struma Ovarii: A Report of Three Cases and Literature Review.卵巢甲状腺肿:三例报告及文献综述
J Midlife Health. 2018 Oct-Dec;9(4):225-229. doi: 10.4103/jmh.JMH_53_18.
5
Struma ovarii accompanied by mature cystic teratoma of the other ovary: A case report and literature review.卵巢甲状腺肿伴对侧卵巢成熟囊性畸胎瘤:一例报告及文献复习
Oncol Lett. 2015 May;9(5):2053-2055. doi: 10.3892/ol.2015.3029. Epub 2015 Mar 11.
6
46,XY female sex reversal syndrome with bilateral gonadoblastoma and dysgerminoma.46,XY女性性反转综合征伴双侧性腺母细胞瘤和无性细胞瘤。
Exp Ther Med. 2014 Oct;8(4):1102-1104. doi: 10.3892/etm.2014.1922. Epub 2014 Aug 19.
7
Fetus in fetu: A rare case report.胎中胎:一例罕见病例报告。
J Res Med Sci. 2012 May;17(5):491-4.