Literature DB >> 33593949

Acrodermatitis enteropathica in a 3-month-old boy.

Alexander K C Leung1, Kin Fon Leong2, Joseph M Lam2.   

Abstract

Entities:  

Year:  2021        PMID: 33593949      PMCID: PMC8034336          DOI: 10.1503/cmaj.201181

Source DB:  PubMed          Journal:  CMAJ        ISSN: 0820-3946            Impact factor:   8.262


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A 3-month-old boy who had been exclusively breastfed presented with a 2-week history of diarrhea and diaper rash that had not resolved with barrier cream and frequent changes. The infant was born to a 23-year-old primigravida mother at term on the third centile, which he was growing along. His parents were nonconsanguineous, and there was no known family history of genetic conditions. On physical examination, the infant was irritable and had symmetric, sharply demarcated, erythematous, erosive plaques with scaling and crusting on his toes and genital area (Figure 1A), as well as his cheeks, auricles and neck (Figure 1B). We diagnosed acquired acrodermatitis enteropathica. The diagnosis was supported by a low plasma zinc level (18 [normal 70–120] μg/dL), and low alkaline phosphatase (20 [normal 96–360] U/L). We started zinc supplementation at a dose of 0.5 mg/kg/d. The infant’s symptoms and skin lesions resolved and zinc levels became normal even after zinc supplementation was stopped.
Figure 1:

(A) Multiple well-demarcated erythematous erosive plaques in a 3-month-old boy, involving the toes, genital and perineal areas. (B) Well-defined, crusted erosions on the neck and right auricle. Patchy alopecia of the scalp is also visible.

(A) Multiple well-demarcated erythematous erosive plaques in a 3-month-old boy, involving the toes, genital and perineal areas. (B) Well-defined, crusted erosions on the neck and right auricle. Patchy alopecia of the scalp is also visible. Acrodermatitis enteropathica can be caused by inherited or acquired zinc deficiency.1 When inherited, it is a result of homozygous mutations in the SLC39A4 gene, which lead to impaired zinc transmembrane transport and uptake.2 It occurs in 1 in 500 000 live births, with no predilection for sex or race.3 Typically, bottle-fed infants manifest the symptoms at age 4 to 10 weeks, whereas breastfed infants manifest the symptoms much later because of increased bioavailability of zinc in breast milk, which also contains a zinc transporter protein that facilitates zinc absorption.1 Acquired zinc deficiency most commonly arises from zinc-deficient diets or from breast milk deficient in zinc-binding ligand, and affects 2% of children in the United States and 20% in low- and middle-income countries.1 Physicians should consider measuring serum zinc in infants with irritability, chronic diarrhea, alopecia and typical rash in the periorificial, perineal and acral distribution. Because genetic testing was not available, we made a presumptive diagnosis of acquired acrodermatitis enteropathica based on our patient’s marked response to zinc supplementation. In acquired zinc deficiency, improved maternal diet and maturation of the infant’s gut means zinc levels often remain normal after supplementation is stopped.
  2 in total

1.  Acrodermatitis Enteropathica: A Case Report.

Authors:  Nicolai Nistor; Lavinia Ciontu; Otilia-Elena Frasinariu; Vasile Valeriu Lupu; Ancuta Ignat; Violeta Streanga
Journal:  Medicine (Baltimore)       Date:  2016-05       Impact factor: 1.889

2.  ACRODERMATITIS ENTEROPATHICA: CLINICAL MANIFESTATIONS AND PEDIATRIC DIAGNOSIS.

Authors:  Ieda Regina Lopes Del Ciampo; Regina Sawamura; Luiz Antonio Del Ciampo; Maria Inez Machado Fernandes
Journal:  Rev Paul Pediatr       Date:  2018-01-15
  2 in total

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