Milia-like calcinosis cutis in Down syndrome: a new case with a review of the literature.


Journal

Dermatology online journal
ISSN: 1087-2108
Titre abrégé: Dermatol Online J
Pays: United States
ID NLM: 9610776

Informations de publication

Date de publication:
15 Aug 2021
Historique:
received: 13 09 2021
accepted: 13 09 2021
entrez: 10 11 2021
pubmed: 11 11 2021
medline: 3 2 2022
Statut: epublish

Résumé

We report an 11-year-old girl who presented with white papules on the dorsal and palmar region of the hands bilaterally. The parents reported that the lesions had appeared four months before and some had resolved spontaneously. The girl was suffering from celiac disease, Down syndrome, and alopecia areata treated with topical corticosteroids. At the first visit, the girl presented with alopecia areata, corticosteroid acne, and a dozen white papules located on the hands. On dermoscopy, a whitish structureless area was seen. Histological examination showed the presence of calcium deposits without tissue damage, thus confirming the diagnosis of milia-like idiopathic calcinosis cutis. At 6-month follow up, the lesions had completely disappeared. Milia-like idiopathic calcinosis cutis is a benign cutaneous disorder consisting of calcium deposits in an apparently undamaged dermis and is typically associated with Down syndrome. Up to a quarter of patients have coexisting syringomas. The milia-like papules tend to self-resolve as patients reach adulthood, so a wait-and-see approach is recommended.

Identifiants

pubmed: 34755960
doi: 10.5070/D327854695
doi:

Types de publication

Case Reports Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Agata Moar (A)

Section of Dermatology and Venereology, Department of Medicine, University of Verona, Verona. agata.moar@hotmail.it.

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Classifications MeSH