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未另行指定的恶性卵巢类固醇细胞瘤致一名4岁女童男性化:病例报告及文献综述

Malignant Ovarian Steroid Cell Tumor, Not Otherwise Specified, Causes Virilization in a 4-Year-Old Girl: A Case Report and Literature Review.

作者信息

Yoshimatsu Takaharu, Nagai Kozo, Miyawaki Reiji, Moritani Kyoko, Ohkubo Kazuhiro, Kuwabara Jun, Tatsuta Kyosuke, Kurata Mie, Fukushima Mana, Kitazawa Riko, Hamada Junpei, Ochi Fumihiro, Eguchi-Ishimae Minenori, Tauchi Hisamichi, Eguchi Mariko

机构信息

Department of Pediatrics, Ehime University Graduate School of Medicine, Toon, Japan.

Department of Community and Emergency Medicine, Ehime University Graduate School of Medicine, Toon, Japan.

出版信息

Case Rep Oncol. 2020 Apr 2;13(1):358-364. doi: 10.1159/000506044. eCollection 2020 Jan-Apr.

Abstract

We report a case of a 4-year-old girl with an ovarian steroid cell tumor, not otherwise specified (SCT-NOS). She was admitted to the hospital with progressing virilization and Cushing's syndrome, which included abnormality of the perineum, hirsutism, hypertrichosis, flushing of face, hoarseness, and weight gain. Blood testing showed a significantly increased testosterone level and slightly increased cortisol level. Computed tomography scan revealed an 8.0 × 5.0 × 5.0 cm tumor of the right ovary. The patient underwent right salpingo-oophorectomy, and pathological examination showed malignant potential. Three courses of bleomycin, etoposide, and cisplatin were administered as postoperative chemotherapy. After tumor resection, her testosterone decreased to undetectable levels. However, during the course of the treatment, the patient suffered from adrenal insufficiency resulting in the need for hydrocortisone replacement therapy. Although SCT-NOS in childhood are typically benign, pathological findings should be carefully observed for potential malignancy. In cases of cortisol-producing SCT-NOS, serum levels should be monitored, and hydrocortisone replacement therapy should be considered before resection.

摘要

我们报告一例4岁女童患有未另行指定的卵巢类固醇细胞瘤(SCT-NOS)。她因进行性男性化和库欣综合征入院,表现为会阴异常、多毛症、全身多毛、面部潮红、声音嘶哑和体重增加。血液检测显示睾酮水平显著升高,皮质醇水平略有升高。计算机断层扫描显示右卵巢有一个8.0×5.0×5.0 cm的肿瘤。患者接受了右侧输卵管卵巢切除术,病理检查显示有恶变潜能。术后给予了三个疗程的博来霉素、依托泊苷和顺铂化疗。肿瘤切除后,她的睾酮水平降至检测不到。然而,在治疗过程中,患者出现肾上腺功能不全,需要氢化可的松替代治疗。虽然儿童期的SCT-NOS通常为良性,但应仔细观察病理结果以发现潜在恶变。对于产生皮质醇的SCT-NOS病例,应监测血清水平,并且在切除前应考虑氢化可的松替代治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe6c/7184839/d5f6c5faafab/cro-0013-0358-g01.jpg

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