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青春期后患者的盆腔性腺外卵黄囊瘤:病例报告及影像学分析并文献复习

Extragonadal Pelvic Yolk Sac Tumor in a Postpubertal Patient: Case Report With Radiologic Correlation and Review of the Literature.

作者信息

Jha Saurav, Phillips Emilee, Safran Martin Jumbelic, Gupta Saurabh

机构信息

Department of Radiology Patan Academy of Health Sciences Kathmandu Nepal.

Department of Radiology SUNY Upstate Medical University Hospital New York USA.

出版信息

Clin Case Rep. 2025 Sep 24;13(10):e70939. doi: 10.1002/ccr3.70939. eCollection 2025 Oct.

DOI:10.1002/ccr3.70939
PMID:41001168
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12459076/
Abstract

Yolk sac tumor, also referred to as endodermal sinus tumor, is an aggressive malignant germ cell neoplasm that most commonly originates in the gonad. Its occurrence in extra-gonadal sites is infrequent and is highly malignant, with only a handful of cases reported in the literature. With the help of this article, we want to make readers aware of the rare site of yolk sac tumor, its clinical presentation, and its radiological findings. As clinicians, we should be vigilant to consider differential diagnoses for an underlying etiology, like yolk sac tumor, for a patient presenting with a subcutaneous lump. Even though swelling in subcutaneous regions, in most cases, represents a benign diagnosis, malignant ones should always be kept in the back of the mind while managing patients. Variation in the site of extragonadal germ cell tumors has been highlighted with this paper, and herein, we aim to make readers aware of a rare and uncommon germ cell tumor, acknowledging the importance of imaging findings in making a diagnosis and the approach for its management.

摘要

卵黄囊瘤,也称为内胚窦瘤,是一种侵袭性恶性生殖细胞肿瘤,最常见于性腺。其发生于性腺外部位的情况并不常见,且恶性程度很高,文献中仅报道了少数病例。借助本文,我们希望让读者了解卵黄囊瘤的罕见发病部位、临床表现及其影像学表现。作为临床医生,对于出现皮下肿块的患者,我们应警惕考虑潜在病因(如卵黄囊瘤)的鉴别诊断。尽管皮下区域的肿胀在大多数情况下代表良性诊断,但在治疗患者时,始终应牢记恶性情况。本文强调了性腺外生殖细胞肿瘤发病部位的差异,在此,我们旨在让读者了解一种罕见且不常见的生殖细胞肿瘤,认识到影像学表现在诊断中的重要性及其治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b2/12459076/0efd1b47158c/CCR3-13-e70939-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b2/12459076/7c2ddf2616bb/CCR3-13-e70939-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b2/12459076/adf82f6a00f2/CCR3-13-e70939-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b2/12459076/7218db76ad37/CCR3-13-e70939-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b2/12459076/6044c2399ab6/CCR3-13-e70939-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b2/12459076/8a42e723a463/CCR3-13-e70939-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b2/12459076/8655125a251d/CCR3-13-e70939-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b2/12459076/1f09ada5d9a5/CCR3-13-e70939-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b2/12459076/96fcf7bd1372/CCR3-13-e70939-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b2/12459076/0efd1b47158c/CCR3-13-e70939-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b2/12459076/7c2ddf2616bb/CCR3-13-e70939-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b2/12459076/adf82f6a00f2/CCR3-13-e70939-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b2/12459076/7218db76ad37/CCR3-13-e70939-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b2/12459076/6044c2399ab6/CCR3-13-e70939-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b2/12459076/8a42e723a463/CCR3-13-e70939-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b2/12459076/8655125a251d/CCR3-13-e70939-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b2/12459076/1f09ada5d9a5/CCR3-13-e70939-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b2/12459076/96fcf7bd1372/CCR3-13-e70939-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b2/12459076/0efd1b47158c/CCR3-13-e70939-g005.jpg

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本文引用的文献

1
Phenotypic and Molecular Features of Somatically Derived "Yolk Sac Tumors": Similarities and Differences With Counterparts of Germ Cell Origin.体细胞来源“卵黄囊瘤”的表型和分子特征:与生殖细胞来源对应肿瘤的异同
Mod Pathol. 2025 Jun 6;38(9):100807. doi: 10.1016/j.modpat.2025.100807.
2
Analysis of HNF1β expression suggests that its downregulation is involved in the sarcomatoid transformation of yolk sac tumor.HNF1β表达分析表明,其下调与卵黄囊瘤的肉瘤样转化有关。
Virchows Arch. 2025 Feb 24. doi: 10.1007/s00428-025-04062-0.
3
Paratesticular/inguinal SMARCB1/INI1 deficient carcinomas with yolk sac tumour-like differentiation are aggressive somatic malignancies.
伴有卵黄囊瘤样分化的睾丸旁/腹股沟SMARCB1/INI1缺陷型癌是侵袭性实体恶性肿瘤。
Histopathology. 2025 Jun;86(7):1044-1052. doi: 10.1111/his.15410. Epub 2025 Jan 6.
4
Ultrasonographic and clinicopathological features of pelvic yolk sac tumors in women: a single-center retrospective analysis.女性盆腔卵黄囊瘤的超声及临床病理特征:单中心回顾性分析
Front Oncol. 2024 Jun 20;14:1417761. doi: 10.3389/fonc.2024.1417761. eCollection 2024.
5
Yolk Sac Tumor in an Eight-Year-Old Girl: A Case Report and Literature Review.一名八岁女孩的卵黄囊瘤:病例报告及文献综述
Front Pediatr. 2019 Apr 30;7:169. doi: 10.3389/fped.2019.00169. eCollection 2019.
6
Successful treatment of advanced stage yolk sac tumour of extragonadal origin: a case report and review of literature.性腺外起源晚期卵黄囊瘤的成功治疗:一例报告并文献复习
Acta Med Litu. 2016;23(2):110-116. doi: 10.6001/actamedica.v23i2.3327.
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Yolk sac tumor in the abdominal wall of an 18-month-old girl: a case report.18个月女童腹壁卵黄囊瘤:一例报告
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Yolk sac tumor of the ovary: a retrospective multicenter study of 33 Japanese women by Tohoku Gynecologic Cancer Unit (TGCU).卵巢卵黄囊瘤:东北妇科癌症研究组(TGCU)对 33 名日本女性进行的回顾性多中心研究。
Tohoku J Exp Med. 2013 Aug;230(4):211-7. doi: 10.1620/tjem.230.211.
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J Obstet Gynaecol Res. 2012 Mar;38(3):605-9. doi: 10.1111/j.1447-0756.2011.01752.x. Epub 2012 Feb 22.
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Afr J Paediatr Surg. 2011 May-Aug;8(2):241-3. doi: 10.4103/0189-6725.86074.