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[Cutaneous hyperpigmentation secondary to vitamin B12 deficiency in an infant].

作者信息

Viada Pelaez María C, Buján María M, Cervini Andrea B

机构信息

Servicio de Dermatología, Hospital Nacional de Pediatría "Prof. Dr. Juan P. Garrahan", Ciudad de Buenos Aires, Argentina.

出版信息

Arch Argent Pediatr. 2020 Feb;118(1):e63-e66. doi: 10.5546/aap.2020.e63.

DOI:10.5546/aap.2020.e63
PMID:31984713
Abstract

Cutaneous hyperpigmentation is a rare clinical feature of vitamin B12 (cobalamin) deficiency. The cause is unknown and there are different hypothesis about the pathogenesis of the hyperpigmentation. We report the case of an 8-month-old girl, with history of neuromadurative delay, hypotonia, anemia and neutropenia, who was referred to our Service by brownish hyperpigmentation on her hands and feet of 3 months of evolution. Based on the clinical suspicion of vitamin B12 deficiency, we performed a laboratory dosage that showed decreased levels of cobalamin, reason for which replacement therapy was indicated. It highlights the importance of the presumption of vitamin B12 deficiency as a cause of cutaneous hyperpigmentation and its rapid resolution after the establishment of the appropriate treatment.

摘要

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Arch Argent Pediatr. 2020 Feb;118(1):e63-e66. doi: 10.5546/aap.2020.e63.
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