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妊娠黄体瘤合并子宫平滑肌瘤:诊断挑战及卵巢恶性肿瘤的模仿者——来自印度农村的罕见病例

Luteoma of Pregnancy with Uterine Leiomyoma as a Diagnostic Challenge and Mimicker of Ovarian Malignancy: A Rare Case From Rural India.

作者信息

Dayal Seema

机构信息

Department of Pathology, Uttar Pradesh University of Medical Sciences, Saifai, Etawah, India.

出版信息

J Reprod Infertil. 2022 Jan-Mar;23(1):67-70. doi: 10.18502/jri.v23i1.8455.

Abstract

BACKGROUND

Luteoma of pregnancy is a rare, non-neoplastic lesion of the ovary which mimics ovarian tumor. It develops hirsutism or virilization during pregnancy and regresses in postpartum phase spontaneously. A few number of cases are described in literature. The synchronization of ovarian luteoma with uterine leiomyomas is a rare condition; to the best of my knowledge, the association of both conditions is not reported till date.

CASE PRESENTATION

A 35 year old multiparous woman presented with mass and pain in abdomen came to the gynecology department of Uttar Pradesh University of Medical Sciences in India. On examination, a hard mass in uterus was diagnosed. Ultrasonography revealed a highly vascular uterine adnexal mass possibly arising from ovary with malignant features. Hysterectomy with bilateral salpingo-oophorectomy was done and this specimen with separate mass was sent for histopathology. Right sided ovary was measured 3×3 , well demarcated with solid brown areas. CA -125 (cancer antigen -125) level was raised. A separate tumor was measured 15×12×8 and it was smooth while cut surface was grey/white with whirling and hemorrhagic foci.

RESULTS

The section from ovary revealed luteoma of pregnancy. Endometrium microscopy confirmed pregnancy. Section from another mass/tumor showed leiomyoma with degenerations.

CONCLUSION

Pregnancy luteoma is a pregnancy induced lesion which mimics malignancy so, it is clinically misinterpreted and over diagnosed. Histopathological investigation is mandatory to diagnose and prevent unnecessary surgeries. The synchronous ovarian luteoma with uterine leiomyoma is a rare condition which represents unusual response to altered hormonal effect in pregnancy; therefore, more studies should be done to understand its pathogenesis.

摘要

背景

妊娠黄体瘤是一种罕见的卵巢非肿瘤性病变,可模仿卵巢肿瘤。它在孕期出现多毛症或男性化,并在产后阶段自行消退。文献中描述的病例数量较少。卵巢黄体瘤与子宫平滑肌瘤同时出现是一种罕见情况;据我所知,至今尚未报道过这两种情况的关联。

病例介绍

一名35岁经产妇因腹部肿块和疼痛就诊于印度北方邦医学科学大学妇科。检查时,诊断出子宫有一个硬肿块。超声检查显示子宫附件有一个高度血管化的肿块,可能起源于卵巢,具有恶性特征。进行了子宫切除术及双侧输卵管卵巢切除术,并将带有单独肿块的标本送去做组织病理学检查。右侧卵巢大小为3×3,界限清楚,有实性棕色区域。癌抗原125(CA -125)水平升高。另一个单独的肿瘤大小为15×12×8,表面光滑,切面为灰白色,有漩涡状和出血灶。

结果

卵巢切片显示为妊娠黄体瘤。子宫内膜显微镜检查证实为妊娠。另一个肿块/肿瘤的切片显示为有退变的平滑肌瘤。

结论

妊娠黄体瘤是一种模仿恶性肿瘤的妊娠诱导性病变,因此在临床上容易被误解和过度诊断。组织病理学检查对于诊断和避免不必要的手术是必不可少的。卵巢黄体瘤与子宫平滑肌瘤同时出现是一种罕见情况,代表了对孕期激素变化的异常反应;因此,需要进行更多研究以了解其发病机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3084/9361728/5e79df2bd2cd/JRI-23-67-g001.jpg

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