• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

卵巢畸胎瘤合并肾母细胞瘤腹部转移 1 例报告

A case of ovarian Teratoma with nephroblastoma presenting abdomen metastasis.

机构信息

Department of Pathology, Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research, The Affiliated Cancer Hospital of Nanjing Medical University, Nanjing, China.

Obstetrical Department, Lianyungang Maternal and Child Health Hospital, Lianyungang, China.

出版信息

J Clin Lab Anal. 2022 May;36(5):e24364. doi: 10.1002/jcla.24364. Epub 2022 Mar 29.

DOI:10.1002/jcla.24364
PMID:35349728
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9102504/
Abstract

BACKGROUND

Teratoma with nephroblastoma (TWN) is an extremely rare condition. Since 1984, only 45 reported cases have been identified. To our knowledge, there have been only two cases of TWN of ovarian origin.

CASE PRESENTATION

We described a case of ovarian TWN who presented to us with painless abdominal masses 6 months after undergoing right ovarian cystectomy. The tumor had spread to the abdomen due to spontaneous rupture of the ovarian cyst and failure to undergo chemotherapy. Microscopically, the ovarian mass exhibited the typical components of a mature cystic teratoma. The tumors found in both the ovary and abdomen contained the nephroblastoma components and were strongly positive for WT-1. The patient was advised to undergo chemotherapy and she was lost to follow-up.

CONCLUSION

A careful histological examination is necessary for an accurate diagnosis, which is based on morphology and extensive immunohistochemical studies. According to the literature, surgical excision alone seems reasonable as the prognosis of TWN is considered to be good. However, due to the spontaneous rupture of the ovarian cyst, chemotherapy of the patient after the first surgery was necessary in our case. Therefore, additional case studies are needed to clarify the standardized treatment of TWN.

摘要

背景

畸胎瘤合并肾母细胞瘤(TWN)是一种极其罕见的情况。自 1984 年以来,仅确认了 45 例报告病例。据我们所知,仅有两例卵巢起源的 TWN 病例。

病例介绍

我们描述了一例卵巢 TWN 患者,她在右侧卵巢囊肿切除术后 6 个月因无痛性腹部肿块就诊。由于卵巢囊肿自发破裂和未接受化疗,肿瘤已扩散至腹部。显微镜下,卵巢肿块表现出成熟囊性畸胎瘤的典型成分。在卵巢和腹部发现的肿瘤均含有肾母细胞瘤成分,并对 WT-1 呈强阳性。建议患者接受化疗,但她失访。

结论

准确的诊断需要仔细的组织学检查,其依据是形态学和广泛的免疫组织化学研究。根据文献,单独进行手术切除似乎是合理的,因为 TWN 的预后被认为是良好的。然而,由于卵巢囊肿的自发破裂,我们的病例中患者在第一次手术后需要进行化疗。因此,需要进一步的病例研究来阐明 TWN 的标准化治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81d5/9102504/c58c36d48045/JCLA-36-e24364-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81d5/9102504/b9f34a9cb2c8/JCLA-36-e24364-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81d5/9102504/c84e62adc72f/JCLA-36-e24364-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81d5/9102504/c58c36d48045/JCLA-36-e24364-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81d5/9102504/b9f34a9cb2c8/JCLA-36-e24364-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81d5/9102504/c84e62adc72f/JCLA-36-e24364-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81d5/9102504/c58c36d48045/JCLA-36-e24364-g004.jpg

相似文献

1
A case of ovarian Teratoma with nephroblastoma presenting abdomen metastasis.卵巢畸胎瘤合并肾母细胞瘤腹部转移 1 例报告
J Clin Lab Anal. 2022 May;36(5):e24364. doi: 10.1002/jcla.24364. Epub 2022 Mar 29.
2
A case of ovarian teratoma with nephroblastoma presenting spontaneous rupture.1例卵巢畸胎瘤合并肾母细胞瘤自发破裂。
J Obstet Gynaecol Res. 2019 May;45(5):1079-1083. doi: 10.1111/jog.13887. Epub 2019 Jan 30.
3
Autoamputation of an ovarian mature cystic teratoma: a case report and a review of the literature.卵巢成熟囊性畸胎瘤自行脱落:一例报告并文献复习
World J Surg Oncol. 2016 Aug 17;14(1):217. doi: 10.1186/s12957-016-0981-7.
4
Wilms Tumor of the Ovary: Review of the Literature and Report of 2 Cases.卵巢 Wilms 瘤:文献复习及 2 例报告。
Int J Gynecol Pathol. 2020 Jan;39(1):72-78. doi: 10.1097/PGP.0000000000000565.
5
Extrarenal teratoma with nephroblastoma in the retroperitoneum: Case report and literature review.腹膜后肾外畸胎瘤合并肾母细胞瘤:病例报告及文献复习
Medicine (Baltimore). 2017 Nov;96(46):e8670. doi: 10.1097/MD.0000000000008670.
6
Spontaneous rupture of benign ovarian cystic teratoma in a premenarcheal girl.一名青春期前女孩的良性卵巢囊性畸胎瘤自发性破裂。
J Pediatr Adolesc Gynecol. 2009 Oct;22(5):e121-3. doi: 10.1016/j.jpag.2008.09.006. Epub 2009 Jul 3.
7
Rupture of a mature cystic teratoma in a young girl caused by a car accident: an extremely rare case and review of the literature.年轻女孩因车祸导致成熟囊性畸胎瘤破裂:一例极其罕见的病例并文献复习。
Folia Med (Plovdiv). 2021 Jun 30;63(3):438-442. doi: 10.3897/folmed.63.e55388.
8
Unusual presentation of plasmablastic lymphoma involving ovarian mature cystic teratoma: a case report.累及卵巢成熟囊性畸胎瘤的浆母细胞淋巴瘤的罕见表现:一例报告
Diagn Pathol. 2017 Nov 29;12(1):83. doi: 10.1186/s13000-017-0672-x.
9
Co-Existing Ovarian Mucinous Cystadenocarcinoma with Mature Cystic Teratoma: A Rare Case Report.卵巢黏液性囊腺癌合并成熟性囊性畸胎瘤:1例罕见病例报告
J Med Assoc Thai. 2016 Jul;99 Suppl 4:S281-6.
10
Malignant transformation from mature cystic teratoma of the ovary.卵巢成熟性囊性畸胎瘤的恶性转化
J Obstet Gynaecol Res. 2019 Sep;45(9):1957-1960. doi: 10.1111/jog.14043. Epub 2019 Jun 19.

引用本文的文献

1
Wilms' Tumor: A Review of Clinical Characteristics, Treatment Advances, and Research Opportunities.肾母细胞瘤:临床特征、治疗进展及研究机会综述
Medicina (Kaunas). 2025 Mar 12;61(3):491. doi: 10.3390/medicina61030491.
2
Teratoma-associated and so-called pure Wilms tumour of the ovary represent two separate tumour types with distinct molecular features.畸胎瘤相关和所谓的卵巢单纯 Wilms 瘤是两种具有不同分子特征的独立肿瘤类型。
Histopathology. 2024 Mar;84(4):683-696. doi: 10.1111/his.15116. Epub 2023 Dec 12.
3
Testicular teratoma with nephroblastoma in an adult - case report and literature review.

本文引用的文献

1
Impact of the First Generation of Children's Oncology Group Clinical Trials on Clinical Practice for Wilms Tumor.第一代儿童肿瘤学组临床试验对肾母细胞瘤临床实践的影响。
J Natl Compr Canc Netw. 2021 Aug 1;19(8):978-985. doi: 10.6004/jnccn.2021.7070.
2
Alveolar rhabdomyosarcoma with unusual cytogenetic findings: one more case and review of the literature.具有不寻常细胞遗传学发现的肺泡横纹肌肉瘤:又一例病例及文献复习
Oxf Med Case Reports. 2019 Nov 18;2019(10):omz107. doi: 10.1093/omcr/omz107. eCollection 2019 Oct.
3
A case of ovarian teratoma with nephroblastoma presenting spontaneous rupture.
成人睾丸畸胎瘤合并肾母细胞瘤——病例报告及文献综述
Contemp Oncol (Pozn). 2023;27(1):60-63. doi: 10.5114/wo.2023.127193. Epub 2023 Apr 27.
4
A case of immature teratoma with nephroblastic components in the oral cavity of a cat.一例口腔内具有肾母细胞成分的不成熟畸胎瘤病例。
J Vet Med Sci. 2023 Mar 30;85(4):420-424. doi: 10.1292/jvms.23-0023. Epub 2023 Mar 27.
1例卵巢畸胎瘤合并肾母细胞瘤自发破裂。
J Obstet Gynaecol Res. 2019 May;45(5):1079-1083. doi: 10.1111/jog.13887. Epub 2019 Jan 30.
4
Kidney teratoma: A case report and literature review.肾畸胎瘤:一例病例报告及文献综述
Urol Case Rep. 2018 Jul 12;20:83-84. doi: 10.1016/j.eucr.2018.07.012. eCollection 2018 Sep.
5
Teratoid Wilms Tumor: Report of Three Cases and Review of the Literature.畸胎样肾母细胞瘤:三例报告并文献复习
Turk Patoloji Derg. 2019;35(1):61-68. doi: 10.5146/tjpath.2016.01363.
6
Wilms' tumor of the ovary.卵巢威尔姆斯瘤
Gynecol Oncol Rep. 2016 Dec 14;19:18-21. doi: 10.1016/j.gore.2016.12.004. eCollection 2017 Feb.
7
Alveolar rhabdomyosarcoma of maxilla.上颌骨肺泡状横纹肌肉瘤
J Oral Maxillofac Pathol. 2016 Jan-Apr;20(1):164. doi: 10.4103/0973-029X.180987.
8
Sacrococcygeal teratoma with nephroblastic elements: a case report and review of literature.伴有肾母细胞瘤成分的骶尾部畸胎瘤:一例报告并文献复习
Int J Clin Exp Pathol. 2014 Oct 15;7(11):8211-6. eCollection 2014.
9
Teratoid Wilms' tumor exhibiting extensive squamous differentiation.呈现广泛鳞状分化的畸胎样肾母细胞瘤。
Fetal Pediatr Pathol. 2015 Feb;34(1):70-2. doi: 10.3109/15513815.2014.925019. Epub 2014 Jun 19.
10
Teratoid Wilms' tumor in a child: A report of a rare case.儿童畸胎样肾母细胞瘤:1例罕见病例报告
Int J Appl Basic Med Res. 2013 Jan;3(1):72-4. doi: 10.4103/2229-516X.112248.