Chronic cutaneous candidiasis in children: should we stop there? Report of two cases associated with auto-immune polyendocrinopathy syndrome type I.

Abstract:

BACKGROUND:Auto-immune polyendocrinopathy syndrome type I is a rare genetic disease, usually revealed by chronic superficial candidiasis and autoimmune endocrine dysfunction in childhood. CASES PRESENTATION:We report the cases of 2 children, a 4 years-11 months old boy and 13 years old adolescent, admitted and followed up in the endocrinology unit of the Mother and Child Centre of Chantal Biya's Foundation for auto-immune polyendocrine syndrome type 1. CONCLUSION:The occurrence of chronic cutaneous candidiasis in a child should always imply endocrine screening, to exclude auto-immune polyendocrine syndrome type I.

journal_name

BMC Pediatr

journal_title

BMC pediatrics

authors

Minka BM,Sibetcheu T A,Sap SNU,Bissa MC

doi

10.1186/s12887-020-02030-y

subject

Has Abstract

pub_date

2020-03-18 00:00:00

pages

128

issue

1

issn

1471-2431

pii

10.1186/s12887-020-02030-y

journal_volume

20

pub_type

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