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本文引用的文献

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Ovarian Dysgerminoma in Pregnant Women with Viable Fetus: A Rare Case Report.怀有存活胎儿的孕妇发生卵巢无性细胞瘤:一例罕见病例报告
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2
Pregnancy with giant ovarian dysgerminoma: A case report and literature review.妊娠合并巨大卵巢无性细胞瘤:1例报告及文献复习
Medicine (Baltimore). 2020 Oct 9;99(41):e21214. doi: 10.1097/MD.0000000000021214.
3
Ovarian dysgerminoma in pregnancy: A case report and literature review.妊娠性卵巢未成熟畸胎瘤:病例报告及文献复习。
Cancer Biol Ther. 2018 Aug 3;19(8):649-658. doi: 10.1080/15384047.2018.1450118. Epub 2018 Apr 25.
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Pure gonadal dysgenesis (46 XX type) with a familial pattern.具有家族性模式的单纯性腺发育不全(46 XX型)。
Adv Biomed Res. 2015 Aug 10;4:162. doi: 10.4103/2277-9175.162536. eCollection 2015.
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Feto-maternal outcomes of pregnancy complicated by ovarian malignant germ cell tumor: a systematic review of literature.妊娠合并卵巢恶性生殖细胞肿瘤的母胎结局:文献系统综述
Eur J Obstet Gynecol Reprod Biol. 2014 Oct;181:145-56. doi: 10.1016/j.ejogrb.2014.07.047. Epub 2014 Aug 7.
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A pelvic mass on ultrasonography and high human chorionic gonadotropin level: not always an ectopic pregnancy.超声检查发现盆腔肿块且人绒毛膜促性腺激素水平升高:不一定是异位妊娠。
BMJ Case Rep. 2012 Jun 1;2012:bcr0120125577. doi: 10.1136/bcr.01.2012.5577.
8
Fine needle aspiration diagnosis of bilateral dysgerminoma with syncytiotrophoblastic giant cells.细针穿刺诊断双侧无性细胞瘤伴合体滋养层巨细胞。
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SALL4 is a novel sensitive and specific marker of ovarian primitive germ cell tumors and is particularly useful in distinguishing yolk sac tumor from clear cell carcinoma.SALL4是卵巢原始生殖细胞肿瘤一种新的敏感且特异的标志物,在鉴别卵黄囊瘤和透明细胞癌方面尤为有用。
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10
Dysgerminoma of the ovary with precocious puberty: a case report.卵巢无性细胞瘤伴性早熟:一例报告
Gynecol Endocrinol. 2007 Jan;23(1):34-7. doi: 10.1080/09513590601095111.

伴合体滋养层巨细胞的无性细胞瘤合并同期异位妊娠

Dysgerminoma with Syncytiotrophoblastic Giant Cells Associated with a Concurrent Ectopic Pregnancy.

作者信息

Aden Durre, Saeed Noora, Hassan Mahboob, Haiyat Sadaf

机构信息

Department of Pathology, Jawaharlal Nehru Medical College and Hospital, AligarhMuslimUniversity, Aligarh, Uttar Pradesh India.

Department of Pathology, HIMSR, Jamia Hamdard, Delhi, India.

出版信息

Indian J Surg Oncol. 2024 Sep;15(3):531-535. doi: 10.1007/s13193-024-01945-7. Epub 2024 May 1.

DOI:10.1007/s13193-024-01945-7
PMID:39239441
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11371978/
Abstract

BACKGROUND

Dysgerminomas constitute around 1-2% of all germ cell tumours. It is very very rare to have dysgerminoma with concurrent pregnancy with an incidence of 0.2-1 per 100,000 pregnancies. It is extremely difficult to conceive with no assisted reproductive interventions and carry it till completion with no complications in a concurrent dysgerminoma. Dysgerminoma has a characteristic specific histomorphology and is easy to diagnose. However, occasionally, syncytiotrophoblastic differentiation can be seen in dysgerminoma although it is a rare histopathological finding. Also, the raised serum B-HCG levels due to the syncytiotrophoblast giant cells seen can lead to a diagnostic dilemma.

CLINICAL PRESENTATION

Here we report a case of a 27-year-old 8-week pregnant female who came to the hospital with chief complaints of left-sided abdominal pain and a lump abdomen. Clinical and radiological examination revealed a left ovarian tumour of malignant aetiology with the presence of right ectopic pregnancy. A staging laparotomy with left salpingoophorectomy was performed and sent for histopathological examination. It was reported as dysgerminoma with syncytiotrophoblastic giant cells. The right fallopian tube showed products of conception. Finally, she was planned for adjuvant chemotherapy and serial B-HCG levels.

SUMMARY

This case is reported not only just for its rare histopathological finding but also for the diagnostic dilemma it causes both to the surgeon as well as the pathologist. There are various factors which can act as prognosticators such as early suspicion of a tumor, radiological findings, surgery, histopathological examination, and oncology team.

摘要

背景

无性细胞瘤约占所有生殖细胞肿瘤的1%-2%。无性细胞瘤合并妊娠极为罕见,发生率为每10万次妊娠中有0.2-1例。在没有辅助生殖干预的情况下,无性细胞瘤患者很难受孕,并且在合并无性细胞瘤的情况下顺利妊娠至足月且无并发症极为困难。无性细胞瘤具有特征性的组织形态学表现,易于诊断。然而,尽管合体滋养层分化在无性细胞瘤中是一种罕见的组织病理学发现,但偶尔也可见到。此外,由于可见合体滋养层巨细胞导致血清β-HCG水平升高,可引起诊断困境。

临床表现

在此,我们报告一例27岁、孕8周的女性患者,她因左侧腹痛和腹部肿块为主诉前来医院就诊。临床和影像学检查发现左侧卵巢有恶性肿瘤,同时存在右侧异位妊娠。进行了分期剖腹手术及左侧输卵管卵巢切除术,并送去做组织病理学检查。报告为伴有合体滋养层巨细胞的无性细胞瘤。右侧输卵管可见妊娠产物。最后,她被安排进行辅助化疗并监测血清β-HCG水平。

总结

报告该病例不仅是因其罕见的组织病理学发现,还因其给外科医生和病理学家带来的诊断困境。有多种因素可作为预后指标,如对肿瘤的早期怀疑、影像学检查结果、手术、组织病理学检查以及肿瘤学团队。