Acrodermatitis dysmetabolica secondary to isoleucine deficiency in infant with maple syrup urine disease


Submitted: 17 May 2023
Accepted: 1 July 2023
Published: 9 August 2023
Abstract Views: 509
PDF: 294
HTML: 232
Publisher's note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

Authors

Acrodermatitis dysmetabolica (AD) describes eruptions characterized by the clinical triad of acral dermatitis, diarrhea, and alopecia. AD can be caused by various metabolic disorders, one of which is maple syrup urine disease (MSUD). We present a 2- month-old boy diagnosed with MSUD by the age of 5 days and treated with branched-chain amino acid (BCAA) restricted diet, BCAAs formula, and thiamine supplementation. He was referred to dermatology with a 3-week history of diarrhea, progressive acrodermatitis enteropathica like cutaneous eruption and hair loss over the scalp treated with topical mometasone ointment, isoleucine supplementation and leucine restriction. Complete resolution of skin eruption was achieved by 4 weeks, which correlates with normalization of BCAA levels based on close monitoring of biochemical lab values and growth. This case emphasizes the dangers of limiting BCAA intake when treating MSUD, as well as the importance of close monitoring during the amino acid depleting period of growth.


​Flores K, Chikowski R, Morrell DS. Acrodermatitis dysmetabolica in an infant with maple syrup urine disease. Clin Exp Dermatol 2016;41:651-4.

​Rosa J, Fraga AB, de Carvalho R, et al. Acrodermatitis dysmetabolica as a sign of methylmalonic aciduria decompensation. Clin Case Rep 2018;6:1048-50.

​Blackburn PR, Gass JM, Pinto e Vairo F, et al. Maple syrup urine disease: mechanisms and management. Vol. 10. Application of clinical genetics. Dove Medical Press Ltd.; 2017. p. 57–66.

​Burrage LC, Nagamani SC, Campeau PM, Lee BH. Branched-chain amino acid metabolism: from rare mendelian diseases to more common disorders. 2014. Available from: http://hmg.oxfordjournals.org/

​Tabanliog̀lu D, Ersoy-Evans S, Karaduman A. Acrodermatitis enteropathica-like eruption in metabolic disorders: Acrodermatitis dysmetabolica is proposed as a better term. Pediatr Dermatol 2009;26:150-4.

​Gupta N, Jain P, Kabra M, et al. Acrodermatitis dysmetabolica - report of two cases. Vol. 82. Indian J Pediatr 2015:869-70.

​Abad RMR, Pauline J, Lazo-Dizon H. A 1-year-old female with maple syrup urine disease presenting with acrodermatitis-enteropathica-like lesions. Acta Med Philipp 2023;52.

Alkhayal, F. A., Al Haddad , S., Bakraa , R. M., & Alqahtani , A. (2023). Acrodermatitis dysmetabolica secondary to isoleucine deficiency in infant with maple syrup urine disease. Dermatology Reports, 15(4). https://doi.org/10.4081/dr.2023.9750

Downloads

Download data is not yet available.

Citations