Hamarsheh Maysam Jehad Yousef, Melhem Layan, Nazzal Raed, Ghannam Asmaa
Obstetrics and Gynaecology Residency Program, Department of Obstetrics and Gynaecology, Ibn Sina Hospital, Jenin, West Bank, Palestine.
Department of Pathology, Ibn Sina Hospital, Jenin, West Bank, Palestine.
Int J Surg Case Rep. 2025 Sep 18;136:111947. doi: 10.1016/j.ijscr.2025.111947.
Mucinous cystadenoma of the ovary is a benign epithelial tumor. Its coexistence with stromal Leydig cell hyperplasia during pregnancy is extremely rare. Hormonal shifts during gestation may contribute to stromal changes, yet the clinical significance of such findings remains unclear.
A 21-year-old gravida 2, para 1 woman at 38 + 4 weeks' gestation underwent elective cesarean section. Intraoperatively, a 7 × 5 cm left ovarian cyst was identified and excised. The contralateral ovary appeared normal. Histopathology confirmed mucinous cystadenoma with stromal Leydig cell hyperplasia. The patient was asymptomatic, with no signs of virilization. No serum androgen testing was performed, and she recovered uneventfully postpartum.
Mucinous cystadenomas are common benign ovarian tumors, while stromal Leydig cell hyperplasia is rare and often hormonally active. Their coexistence in a pregnant patient without androgenic symptoms is highly unusual. Human chorionic gonadotropin (hCG), known for its LH-like activity, may stimulate Leydig cell proliferation. The absence of clinical virilization could be attributed to low androgen output or increased sex hormone-binding globulin levels in pregnancy.
This case emphasizes the need for vigilance during cesarean sections, the value of histopathological evaluation in incidental adnexal findings, and raises questions about hormonal influences on rare ovarian stromal pathologies in pregnancy.
卵巢黏液性囊腺瘤是一种良性上皮性肿瘤。其在妊娠期间与间质Leydig细胞增生并存极为罕见。妊娠期间的激素变化可能导致间质改变,然而这些发现的临床意义仍不明确。
一名21岁、孕2产1的女性,妊娠38 + 4周时接受择期剖宫产。术中发现并切除了一个7×5 cm的左侧卵巢囊肿。对侧卵巢外观正常。组织病理学证实为黏液性囊腺瘤伴间质Leydig细胞增生。患者无症状,无男性化体征。未进行血清雄激素检测,产后恢复顺利。
黏液性囊腺瘤是常见的良性卵巢肿瘤,而间质Leydig细胞增生罕见且通常具有激素活性。它们在一名无雄激素症状的妊娠患者中共存非常罕见。人绒毛膜促性腺激素(hCG)具有类似LH的活性,可能刺激Leydig细胞增殖。无临床男性化表现可能归因于妊娠期间雄激素分泌量低或性激素结合球蛋白水平升高。
该病例强调了剖宫产时保持警惕的必要性、对偶然附件发现进行组织病理学评估的价值,并引发了关于激素对妊娠期间罕见卵巢间质病变影响的疑问。