Mucinous adenocarcinoma arising from a mature cystic teratoma of the ovary in a pediatric patient: A rare case report

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.

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Publication Details

Journal
Radiology Case Reports
Published
2025-08-22
DOI
https://doi.org/10.1016/j.radcr.2025.07.055
Primary Topic
Ovarian cancer diagnosis and treatment
Type
article
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article

Mucinous adenocarcinoma arising from a mature cystic teratoma of the ovary in a pediatric patient: A rare case report

Saniya Ishtiaq, Shahroze Ahmed, Malak Nawaz Khan Khattak, Muhammad Junaid Tahir et al.
Radiology Case Reports
Ovarian cancer diagnosis and treatment
article

Mucinous adenocarcinoma arising from a mature cystic teratoma of the ovary in a pediatric patient: A rare case report

Saniya Ishtiaq, Shahroze Ahmed, Malak Nawaz Khan Khattak, Muhammad Junaid Tahir, Khadeeja Anwar, Kashif Siddique
article en

Abstract

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.

Radiology Case ReportsVol. 20(11)
Shaukat Khanum Memorial Cancer Hospital and Research Center (PK)
Zero hunger
Openalex Percentile: Top 71%
Ovarian cancer diagnosis and treatment
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