Sex Cord-Stromal Tumours in Children: A Case Series

Sex cord-stromal tumours (SCSTs) in children are rare gonadal neoplasms exhibiting differentiation towards sex cord stromal elements. This case series explores paediatric SCSTs, presenting clinical, gross, histologic, and immunohistochemical findings, with a focus on limited information available about these tumours in African children. This retrospective study includes 9 cases of ovarian and testicular SCSTs (8 female and 1 male) in patients below 16 years of age. Female patients presented with various SCST subtypes, including juvenile granulosa cell tumours (JGCTs), fibroma, and mixed tumours. Precocious puberty was a common presentation. The male patient had a Leydig cell tumour. Tumour sizes varied, with the smallest in the testis and the largest in a 3-year-old girl. Histologically, most cases exhibited characteristic features of their respective subtypes. Paediatric SCSTs are rare but important considerations in children with gonadal masses. Their incidence in African children is largely unknown. JGCTs are the most prevalent ovarian subtype. Leydig cell tumours are rare in children and can present with virilisation. Mixed SCST-germ cell tumours, though extremely rare, warrant careful consideration and immunohistochemistry for accurate diagnosis.

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Publication Details

Journal
Pediatric and Developmental Pathology
Published
2026-01-30
DOI
https://doi.org/10.1177/10935266251414780
Primary Topic
Testicular diseases and treatments
Type
article
Field-Weighted Citation Impact
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article

Sex Cord-Stromal Tumours in Children: A Case Series

Patricia Okiro, Marc Hendricks, Komala Pillay
Pediatric and Developmental Pathology
Testicular diseases and treatments
article

Sex Cord-Stromal Tumours in Children: A Case Series

Patricia Okiro, Marc Hendricks, Komala Pillay
article en

Abstract

Sex cord-stromal tumours (SCSTs) in children are rare gonadal neoplasms exhibiting differentiation towards sex cord stromal elements. This case series explores paediatric SCSTs, presenting clinical, gross, histologic, and immunohistochemical findings, with a focus on limited information available about these tumours in African children. This retrospective study includes 9 cases of ovarian and testicular SCSTs (8 female and 1 male) in patients below 16 years of age. Female patients presented with various SCST subtypes, including juvenile granulosa cell tumours (JGCTs), fibroma, and mixed tumours. Precocious puberty was a common presentation. The male patient had a Leydig cell tumour. Tumour sizes varied, with the smallest in the testis and the largest in a 3-year-old girl. Histologically, most cases exhibited characteristic features of their respective subtypes. Paediatric SCSTs are rare but important considerations in children with gonadal masses. Their incidence in African children is largely unknown. JGCTs are the most prevalent ovarian subtype. Leydig cell tumours are rare in children and can present with virilisation. Mixed SCST-germ cell tumours, though extremely rare, warrant careful consideration and immunohistochemistry for accurate diagnosis.

Pediatric and Developmental Pathology
National Health Laboratory Service (ZA), Western Cape Department of Health (ZA), University of Cape Town (ZA), Aga Khan University Hospital Nairobi (KE), Aga Khan University Nairobi (KE)
Gender equality
Openalex Percentile: Top 73%
Testicular diseases and treatments
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