Ovarian Leydig Cell Tumor Associated with Recurrent Torsion and Virilization in an Adolescent Patient
Document Type
Article
Publication Title
Journal of pediatric and adolescent gynecology
Abstract
Ovarian tumors are rare in children; however, their incidence increases with age. Of these ovarian tumors, Leydig cell tumors are some of the rarest, accounting for less than 0.1% of all ovarian tumors across all ages. Leydig cell tumors predominantly occur in postmenopausal women and are characterized by nodular proliferation of Leydig cells in the ovarian hilum with intracytoplasmic Reinke crystals. These tumors secrete androgens, which can disrupt ovarian function, clinically presenting with abnormal uterine bleeding and virilization. Although they are generally benign, current recommendations are for treatment with a unilateral salpingo-oophorectomy. In adolescents, hyperandrogenism is most commonly caused by polycystic ovarian syndrome (PCOS); however, the differential for hyperandrogenism is broad. We present a case of a 15-year-old girl with a history of primary amenorrhea who presented with a Leydig cell tumor associated with recurrent ovarian torsion and virilization. This case reviews the challenges with diagnosis, management, and future implications of a rare androgen-secreting tumor in young patients.
First Page
217
Last Page
219
DOI
10.1016/j.jpag.2023.11.014
Publication Date
4-1-2024
Recommended Citation
Roth, Lauren; Smith, Anne K.; Buza, Natalia; Coons, Barbara; Stitelman, David; and Vash-Margita, Alla, "Ovarian Leydig Cell Tumor Associated with Recurrent Torsion and Virilization in an Adolescent Patient" (2024). All Research. 12.
https://scholar.bridgeporthospital.org/all_research/12
Identifier
38110028 (pubmed); 10.1016/j.jpag.2023.11.014 (doi); S1083-3188(23)00452-7 (pii)