Panniculitis in Children.
autoinflammatory diseases
histopathology
panniculitis
Journal
Dermatopathology (Basel, Switzerland)
ISSN: 2296-3529
Titre abrégé: Dermatopathology (Basel)
Pays: Switzerland
ID NLM: 101651125
Informations de publication
Date de publication:
01 Aug 2021
01 Aug 2021
Historique:
received:
11
06
2021
revised:
08
07
2021
accepted:
11
07
2021
entrez:
27
8
2021
pubmed:
28
8
2021
medline:
28
8
2021
Statut:
epublish
Résumé
Panniculitides form a heterogenous group of inflammatory diseases that involve the subcutaneous adipose tissue. These disorders are rare in children and have many aetiologies. As in adults, the panniculitis can be the primary process in a systemic disorder or a secondary process that results from infection, trauma or exposure to medication. Some types of panniculitis are seen more commonly or exclusively in children, and several new entities have been described in recent years. Most types of panniculitis have the same clinical presentation (regardless of the aetiology), with tender, erythematous subcutaneous nodules. Although the patient's age and the lesion site provide information, a histopathological assessment is sometimes required for a definitive diagnosis and classification of the disorder. In children, most panniculitides are lobular. At present, autoimmune inflammatory diseases and primary immunodeficiencies have been better characterised; panniculitis can be the presenting symptom in some of these settings. Unexplained panniculitis in a young child should prompt a detailed screen for monogenic immune disorders because the latter usually manifest themselves early in life. Here, we review forms of panniculitis that occur primarily in children, with a focus on newly described entities.
Identifiants
pubmed: 34449587
pii: dermatopathology8030037
doi: 10.3390/dermatopathology8030037
pmc: PMC8395775
doi:
Types de publication
Journal Article
Review
Langues
eng
Pagination
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