Short answer · Medically reviewed summary · Last updated: 2026-05-08
Elastofibroma dorsi is a rare, benign, slow-growing soft tissue tumor most commonly found in the subscapular region. While it is officially recognized as elastofibroma dorsi in modern medical literature, it has historically been referred to as a subscapular elastofibroma or simply elastofibroma. What are the historical and alternative names for Elastofibroma dorsi? Because elastofibroma dorsi was first described in 1959 by Jarvi and Saxen, early medical literature often utilized descriptive terms based on the tumor's location or its histological appearance.
Elastofibroma Dorsi synonyms
Other names for Elastofibroma Dorsi: synonyms, acronyms and related terms used by doctors and patients.
Elastofibroma dorsi is a rare, benign, slow-growing soft tissue tumor most commonly found in the subscapular region. While it is officially recognized as elastofibroma dorsi in modern medical literature, it has historically been referred to as a subscapular elastofibroma or simply elastofibroma.
What are the historical and alternative names for Elastofibroma dorsi?
Because elastofibroma dorsi was first described in 1959 by Jarvi and Saxen, early medical literature often utilized descriptive terms based on the tumor's location or its histological appearance. You may encounter the following synonyms in older medical records or research papers:
- Subscapular elastofibroma: A descriptive term highlighting the anatomical location.
- Elastofibroma: The shortened, generic term often used before the "dorsi" (back) specification became standard.
- Pseudo-tumor of the scapula: An older term reflecting its non-neoplastic, reactive nature.
- Fibroelastoma: An archaic term sometimes used interchangeably in very old texts, though this is medically distinct from modern terminology.
Why does Elastofibroma dorsi have multiple names?
The variation in naming for elastofibroma dorsi stems from the evolution of pathology and imaging. Initially, researchers debated whether the condition was a true neoplasm (tumor) or a reactive hyperplastic process caused by repetitive mechanical friction. As our understanding of the elastic fibers in elastofibroma dorsi improved, the scientific community settled on the current nomenclature to accurately reflect both its histological composition and its primary anatomical site.
What is the official classification of this condition?
In contemporary clinical practice, elastofibroma dorsi is the universally accepted term. It is indexed in major medical databases under the following identifiers:
- ICD-10/11: Classified under benign neoplasms of connective and other soft tissue.
- Orphanet: Recognized under the classification of rare soft tissue tumors.
- OMIM: While elastofibroma dorsi is not assigned a single gene-linked OMIM number, it is documented as a distinct clinical entity in pathology registries.
Next steps
- Consult an orthopedic oncologist or a radiologist to confirm your diagnosis via MRI or CT imaging.
- Connect with the 7 members of our community on DiseaseMaps.org who have shared their experiences with elastofibroma dorsi.
- Discuss with your physician whether observation or surgical excision is appropriate based on your specific symptoms.
Medical disclaimer: This content is for informational purposes only and does not constitute professional medical advice, diagnosis, or treatment.
References
- NIH Genetic and Rare Diseases Information Center (GARD): Elastofibroma dorsi
- Orphanet: Rare soft tissue tumors database
- National Library of Medicine (PubMed): Systematic reviews on elastofibroma dorsi clinical presentation
