揭示不寻常:罕见生殖细胞肿瘤病例系列。

Current health sciences journal Pub Date : 2024-10-01 Epub Date: 2024-12-31 DOI:10.12865/CHSJ.50.04.14
Asmita Chakrabarti, Shailaja Kumari, Moumita Maiti, Chhanda DAS, Gopinath Barui
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引用次数: 0

摘要

生殖细胞肿瘤(gct)是一种异质性肿瘤,起源于原始生殖细胞,可发生在不同部位,最常见于卵巢和睾丸,但由于发育错误,也可在性腺外部位如腹膜后发现。这些肿瘤相对罕见,但由于其潜在的恶性肿瘤和与发育异常相关的临床意义重大。病例介绍:本病例系列报告了四例罕见和不寻常的生殖细胞肿瘤病例,这些病例发生在儿科和成人患者中,每个病例都有独特的临床、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上都是独特的,反映了不同年龄组gct的多样性。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,以及对性腺母细胞瘤,生殖细胞异常瘤,卵巢瘤和胎中胎等罕见疾病的各种治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unveiling the Uncommon: A Case Series on Rare Germ Cell Tumors.

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.

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