Rare case of ovarian Sertoli–Leydig cell tumor in an adolescent: a case report
SLCT is a rare but treatable ovarian tumor. Early detection of androgen excess is crucial. Surgery is effective, and fertility can be preserved. Larger registries are needed to enhance disease understanding and management strategies.
Authors
- Abidemi Junaid (ORCID: https://orcid.org/0000-0001-8562-7942)
- Rabia Zafar (ORCID: https://orcid.org/0000-0002-3515-7441)
- Javeria Taj (ORCID: https://orcid.org/0009-0005-4007-9213)
- Fizza Yousuf
- Hermann Yokolo
Institutions
- Civil Hospital Karachi (PK)
- Dow University of Health Sciences (PK)
- University of Goma (CD)
Publication Details
- Journal
- Annals of Medicine and Surgery
- Published
- 2025-09-01
- DOI
- https://doi.org/10.1097/ms9.0000000000003792
- Citations
- 1
- Primary Topic
- Ovarian cancer diagnosis and treatment
- Type
- article
- Field-Weighted Citation Impact
- 1.70