Khattak Muhammad Jibran, Ahmed Shahroze, Tahir Muhammad Junaid, Anwar Khadeeja, Ishtiaq Shingruff, Siddique Kashif
Department of Radiology, Shaukat Khanum Memorial Cancer Hospital and Research Center, Lahore, Pakistan.
Department of Pathology, Shaukat Khanum Memorial Cancer Hospital and Research Center, Lahore, Pakistan.
Radiol Case Rep. 2025 Aug 22;20(11):5663-5667. doi: 10.1016/j.radcr.2025.07.055. eCollection 2025 Nov.
Mature cystic teratomas (MCTs) are common ovarian neoplasms that rarely undergo malignant transformation, particularly in pediatric patients. We report a rare case of a 5-year-old girl presenting with abdominal distension and back pain, initially managed with incomplete excision of an ovarian mass without histopathological evaluation. Recurrence led to debulking surgery revealing a mixed germ cell tumor, and subsequent imaging identified a residual abdominopelvic mass with elevated alpha-fetoprotein levels. Magnetic resonance imaging (MRI) findings demonstrated a solid-cystic tumor with hemorrhagic components. Complete surgical resection was performed, and histopathology confirmed mucinous adenocarcinoma arising from an MCT. Postoperative imaging showed no residual disease. This case underscores the importance of thorough histopathological analysis, multidisciplinary management, and long-term follow-up in addressing rare and aggressive ovarian tumors in pediatric patients.
成熟囊性畸胎瘤(MCTs)是常见的卵巢肿瘤,很少发生恶性转化,尤其是在儿科患者中。我们报告了一例罕见病例,一名5岁女孩出现腹胀和背痛,最初对卵巢肿块进行了不完全切除,未进行组织病理学评估。复发导致减瘤手术,结果显示为混合性生殖细胞肿瘤,随后的影像学检查发现残留的腹盆腔肿块,甲胎蛋白水平升高。磁共振成像(MRI)结果显示为一个有出血成分的实性囊性肿瘤。进行了完整的手术切除,组织病理学证实为起源于MCT的黏液腺癌。术后影像学检查显示无残留疾病。该病例强调了在处理儿科患者罕见且侵袭性卵巢肿瘤时,进行全面组织病理学分析、多学科管理和长期随访的重要性。