Aden Durre, Saeed Noora, Hassan Mahboob, Haiyat Sadaf
Department of Pathology, Jawaharlal Nehru Medical College and Hospital, AligarhMuslimUniversity, Aligarh, Uttar Pradesh India.
Department of Pathology, HIMSR, Jamia Hamdard, Delhi, India.
Indian J Surg Oncol. 2024 Sep;15(3):531-535. doi: 10.1007/s13193-024-01945-7. Epub 2024 May 1.
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.
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.
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.
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。
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。
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。