Chondromatosis
Classification according to ICD-10 | |
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D48.0 | Chondromatosis |
ICD-10 online (WHO version 2019) |
A Chondromatosis is a disease (of many to very many) which is the formation of multiple Chondromata (as ene or Ekchondrome comes) in the bone or in the joints.
From a osteochondromatosis is used when multiple Chondromata ossify and thus as osteochondroma or (in the case ossified Ekchondrome) as cartilaginous exostosis be called.
Independent clinical pictures are
- the synovial Chondromatosis even Gelenkchondromatose
- the generalized Enchondromatosis , also Enchondromatosis Spranger type VI ; an autosomal - recessive inherited disease
- the Maffucci syndrome , a rare, sporadic Enchondromatosis with hemangiomas and lymphangioma and increased risk of malignancy.
- the Ollier's disease , also Enchondromatosis-Ollier or unilateral multiple Chondromatosis
- the multiple osteochondromatosis , an autosomal dominant inherited disease , usually the metaphyses of the long bones on
Further clinical pictures mentioned in the literature are
- the Metachondromatosis ,
- the Spondyloenchondromatose even Spondyloenchondrodysplasie , Enchondromatosis with spondyloakraler dysplasia
Individual evidence
- ↑ Alphabetical directory for ICD-10-WHO version 2019, volume 3. German Institute for Medical Documentation and Information (DIMDI), Cologne, 2019, p. 154