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primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma

MONDO:0015811

Also known as:Berti lymphomaprimary cutaneous epidermotropic cytotoxic CD8+ T-cell lymphoma

Overview

Primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma is a rare form of primary cutaneous T-cell lymphoma characterized by rapidly progressing, localized or disseminated nodules, tumors or eczematous skin lesions. It has a particularly aggressive clinical course with a high tendency to spread, in advanced stages, to extracutaneous locations (the central nervous system, lung, testes). Lymph nodes are often spared.

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 primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma.

14 publications have been identified in PubMed for primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma. Research spans Case Report / Case Series (57%), Review / Meta-Analysis (29%), and Other (7%).

Research Type	Count	% of Total
Patient case studies	8	57%

Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 9:41 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:178528

GARD

Genetic and Rare Diseases Info Center

GARD:20157

Questions for Your Care Team

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primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma

Overview

Research Landscape

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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