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Progressive osseous heteroplasia in Child
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Progressive osseous heteroplasia in Child

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Contributors: David Sullo MD
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Synopsis

A rare autosomal dominant disorder. Initial manifestation is primary osteoma cutis, a condition of true bone formation within the skin, usually beginning in infancy. Lesions are tender and may ulcerate. Progresses to involve bone formation in deep connective tissue and skeletal muscle. May result in restricted movement and abnormal growth.

For more information, see OMIM.

Codes

ICD10CM:
M61.50 – Other ossification of muscle, unspecified site

SNOMEDCT:
404074003 – Osteoma cutis

Differential Diagnosis & Pitfalls

Best Tests

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References

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Last Updated: 03/29/2017
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Progressive osseous heteroplasia in Child
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Progressive osseous heteroplasia : Subcutaneous nodules
Imaging Studies image of Progressive osseous heteroplasia
Axial CT of the chest demonstrating multiple areas of heterotopic bone formation within the chest wall musculature and ligaments, compatible with myositis ossificans progressiva.
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