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uterine corpus dissecting leiomyoma - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

uterine corpus dissecting leiomyoma

MONDO:0001842

Also known as:Cotyledonoid dissecting leiomyomaSternberg tumorSternberg tumour

Overview

A rare morphologic variant of uterine corpus leiomyoma. Macroscopically, it is characterized by large, fungating, and multinodular neoplasm masses arising from the uterine corpus, and extending into the broad ligament or the peritoneal cavity. Microscopically, it shows neoplastic smooth muscle cells infiltrating the myometrium. The neoplastic cells are arranged in a micronodular pattern. Hydropic changes and increased vascularity are also present.

Diagnosis

Biomarker and diagnostic research for uterine corpus dissecting leiomyoma 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 uterine corpus dissecting leiomyoma.

125 publications have been identified in PubMed for uterine corpus dissecting leiomyoma. Research spans Review / Meta-Analysis (26%), Basic Science / Preclinical (25%), and Clinical Trial Publication (18%).

Research Type	Count	% of Total
Research summaries	32	26%

Data assembled from 2 of 12 sources · Last updated Sep 20, 2026, 3:08 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

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uterine corpus dissecting leiomyoma

Overview

Diagnosis

Research Landscape

Medical References

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Questions for Your Care Team

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