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SAPHO syndrome

variety of inflammatory bone disorders that may be associated with skin changes

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General referenceInterpretive dossier study · Crown Archives visual atlas
Record originEnglish Wikipedia
Text licenseCC BY-SA 4.0
Source revisionFeb 5, 2025
Entity authorityQ1515163 ↗
Source-derived summary

SAPHO syndrome includes a variety of inflammatory bone disorders that may be associated with skin changes. These diseases share some clinical, radiologic, and pathologic characteristics.

An entity initially known as chronic recurrent multifocal osteomyelitis was first described in 1972. Subsequently, in 1978, several cases of were associated with blisters on the palms and soles (palmoplantar pustulosis). Since then, a number of associations between skin conditions and osteoarticular disorders have been reported under a variety of names, including sternocostoclavicular hyperostosis, pustulotic arthro-osteitis, and acne-associated spondyloarthropathy. The term SAPHO (an acronym for synovitis, arthritis, pustulosis, hyperostosis, osteitis) was coined in 1987 to represent this spectrum of inflammatory bone disorders that may or may not be associated with dermatologic pathology.

Diagnosis

Radiologic findings

Anterior chest wall (most common site, 65–90% of patients): Hyperostosis, sclerosis and bone hypertrophy especially involving the sternoclavicular joint, often with a soft tissue component.

Spine (33% of patients): Segmental, usually involving the thoracic spine. The four main presentations include spondylodiscitis, osteosclerosis, paravertebral ossifications, and sacroiliac joint involvement.

Long bones (30% of patients): usually metadiaphyseal and located in the distal femur and proximal tibia.

Editorial summary

“SAPHO syndrome” enters the record as variety of inflammatory bone disorders that may be associated with skin changes. Crown Archives preserves that source wording while asking what SAPHO, syndrome and variety can confirm, complicate or overturn.

Editorial reviewA dependable orientation record for establishing vocabulary, names and a first evidence trail. The current lead gives the account dated anchors—1972, 1978, 1987—that can be checked directly. The selected authority fields contribute no independent date. Its strongest next move is a source search built around SAPHO, syndrome and variety.
Editorial analysis

Why this record matters

“SAPHO syndrome” is worth following because a concise public description often conceals a longer documentary argument. Here, SAPHO, syndrome and variety provides the most credible route into that argument.

Evidence profile

The citation trail is more important than the brevity of the summary: it shows where individual claims can be examined in context. The source revision retrieved here is dated Feb 5, 2025. The linked authority identifier is Q1515163. None of the 0 selected statements returned an explicit reference. The first chronological checks are 1972, 1978 and 1987.

Critical limits

A concise general-reference account can conceal disagreements about scope, terminology or the weight assigned to individual sources. The source lead contains qualifying language; that uncertainty should survive quotation, summary and reuse. Authority statements aid reconciliation but still require their own references, qualifiers and ranks to be checked.

How to read it

Use the entry as an orientation point, then follow its citations and revision history. Names, dates and institutional relationships should be checked against the original record.

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Questions for further research

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Source & attribution

This entry incorporates text from “SAPHO syndrome” on English Wikipedia. Contributors are listed in the page history. Text is available under the Creative Commons Attribution-ShareAlike 4.0 License. Selected authority identifiers and statements are retrieved from Wikidata under CC0; their references and qualifiers remain part of the verification path.