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juvenile type testicular granulosa cell tumor - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

juvenile type testicular granulosa cell tumor

MONDO:0003741

Also known as:juvenile granulosa cell tumorjuvenile granulosa cell tumor (morphologic abnormality)juvenile granulosa cell tumour

Overview

A rare sex cord-stromal tumor that arises from the testis. It is the most frequent congenital testicular neoplasm and is usually diagnosed during the perinatal period. It usually presents as an asymptomatic scrotal or abdominal mass. Morphologically it is characterized by the presence of cysts that are lined by cells resembling granulosa and theca cells.

Diagnosis

Biomarker and diagnostic research for juvenile type testicular granulosa cell tumor has been reported in the published literature.

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for juvenile type testicular granulosa cell tumor.

36 publications have been identified in PubMed for juvenile type testicular granulosa cell tumor. Research spans Case Report / Case Series (81%), Review / Meta-Analysis (11%), and Diagnostic / Biomarker (6%).

Research Type	Count	% of Total
Patient case studies	29	81%

Data assembled from 2 of 12 sources · Last updated Sep 20, 2026, 5:34 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

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juvenile type testicular granulosa cell tumor

Overview

Diagnosis

Research Landscape

Medical References

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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