Cytophagic histiocytic panniculitis
Synonyms: CHP · Winkelmann cytophagic panniculitis
- Type
- Disease
- Group
- Disorder
- Inheritance
- Unknown
- Age of onset
- Adult
- Status
- active
Cytophagic histiocytic panniculitis (CHP) is a very rare form of panniculitis manifesting as recurrent multiple subcutaneous nodules (which may progressively become ecchymotic and ulcerated), and histologically characterized by lobular panniculitis with lymphocytic and histiocytic infiltration in the subcutaneous adipose tissue.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Cytophagic histiocytic panniculitis | CHP · Winkelmann cytophagic panniculitis |
| fr | Panniculite histiocytaire cytophagique | CHP · Panniculite cytophagique de Winkelmann |
| de | Pannikulitis, histiozytäre zytophagische | CHP · Pannikulitis, zytophagische, Typ Winkelmann |
| es | Paniculitis histiocítica citofágica | CHP · Paniculitis citofágica de Winkelmann |
| it | Panniculite citofagica istiocitaria | CHP · Panniculite citofagica di Winkelmann |
| nl | Cytofagische histiocytische panniculitis | CHP · Cytofagische panniculitis van Winkelmann |
| pt | Paniculite citofágica histiocítica | |
| pl | Cytophagic histiocytic panniculitis | CHP |
| cs | Cytofagická histiocytární panikulitida | CHP · Winkelmannova cytofagická panikulitida |
| uk | Цитофагічний гістіоцитарний панікуліт | CHP · Цитофагічний паннікуліт Вінкельмана |
| zh | 组织细胞吞噬性脂膜炎 | Winkelmann吞噬性脂膜炎 |
| tr | Sitofajik histiositik pannikülit | CHP · Winkelmann sitofajik pannikülit |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | M35.8 | NTBT | attributed | validated |
| ICD-11 | EE8Y | NTBT | index | validated |
| MONDO | 0019789 | E | validated | |
| UMLS | C0406594 | E | validated | |
| MedDRA | 10081137 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:79382Subcutaneous tissue disease
rare skin diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | Validated | ORPHANET |
| Cases/families | 100 cases | Worldwide | Case(s) | Validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/94087
- This record as JSON: /data/d/94087.json