Enigma of postmenopausal virilisation: bilateral Leydig cell tumours as the culprit

A postmenopausal woman in her 50s presented with progressive hirsutism, virilisation and markedly elevated serum testosterone levels (>1500 ng/dL). Routine laboratory, adrenal and imaging evaluations were largely unremarkable except for a small left adnexal mass on MRI. With normal dehydroepiandrosterone sulphate (DHEAS) and cortisol levels, an ovarian source of androgen excess was suspected. The patient underwent total laparoscopic hysterectomy with bilateral salpingo-oophorectomy. Histopathology revealed bilateral Leydig cell tumours, an exceptionally rare finding. Postoperatively, serum testosterone normalised, and virilisation regressed significantly. This case highlights the importance of considering androgen-secreting ovarian tumours in postmenopausal women with rapidly progressive virilisation, even when imaging is inconclusive. Bilateral Leydig cell tumours are exceedingly uncommon but should be suspected when severe hyperandrogenism is present. Surgical removal remains the definitive diagnostic and therapeutic approach, ensuring hormonal normalisation and symptom resolution while preventing prolonged morbidity associated with delayed diagnosis.

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Publication Details

Journal
BMJ Case Reports
Published
2026-01-01
DOI
https://doi.org/10.1136/bcr-2025-270645
Primary Topic
Ovarian cancer diagnosis and treatment
Type
article
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article

Enigma of postmenopausal virilisation: bilateral Leydig cell tumours as the culprit

Ishita Roy, Sudwita Sinha, Mukta Agarwal, Avinash Singh
BMJ Case Reports
Ovarian cancer diagnosis and treatment
article

Enigma of postmenopausal virilisation: bilateral Leydig cell tumours as the culprit

Ishita Roy, Sudwita Sinha, Mukta Agarwal, Avinash Singh
article en

Abstract

A postmenopausal woman in her 50s presented with progressive hirsutism, virilisation and markedly elevated serum testosterone levels (>1500 ng/dL). Routine laboratory, adrenal and imaging evaluations were largely unremarkable except for a small left adnexal mass on MRI. With normal dehydroepiandrosterone sulphate (DHEAS) and cortisol levels, an ovarian source of androgen excess was suspected. The patient underwent total laparoscopic hysterectomy with bilateral salpingo-oophorectomy. Histopathology revealed bilateral Leydig cell tumours, an exceptionally rare finding. Postoperatively, serum testosterone normalised, and virilisation regressed significantly. This case highlights the importance of considering androgen-secreting ovarian tumours in postmenopausal women with rapidly progressive virilisation, even when imaging is inconclusive. Bilateral Leydig cell tumours are exceedingly uncommon but should be suspected when severe hyperandrogenism is present. Surgical removal remains the definitive diagnostic and therapeutic approach, ensuring hormonal normalisation and symptom resolution while preventing prolonged morbidity associated with delayed diagnosis.

BMJ Case ReportsVol. 19(1)
Patna Medical College and Hospital (IN), Patna University (IN), All India Institute of Medical Sciences (IN)
Gender equality
Openalex Percentile: Top 96%
Ovarian cancer diagnosis and treatment
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Enigma of postmenopausal virilisation: bilateral Leydig cell tumours as the culprit — Ishita Roy, Sudwita Sinha, et al. · BMJ Case Reports (2026) | TGRS Research Map | TGRS