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J Pediatr Hematol Oncol. 2018 Oct;40(7):e458-e460. doi: 10.1097/MPH.0000000000001073.

A Case With Pyruvate Kinase Deficiency Remarkably Sensitive to Heat.

Author information

1
Department of Pediatric Hematology and Oncology, University of Health Sciences, Ankara Child Health and Diseases Hematology Oncology Training and Research Hospital, Ankara, Turkey.
2
Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Oncoematology Unit, Physiopathology of Anemia Unit, Milan, Italy.

Abstract

Pyruvate kinase (PK) deficiency is the most common defect of the glycolytic pathway leading to congenital hemolytic anemia. We present the case of an 18-year-old boy with chronic nonspherocytic hemolytic anemia, who had remarkable sensitivity to heat. Moreover, the patient showed clinical impairment in the last year. For this reason, we excluded the immunologic or infectious nature (malaria, babesia), which may play a role in the worsening of anemia. Red blood cell enzyme assay showed the presence of a significant increase in other enzyme activities, except for PK, suggesting a PK deficiency in the patient. The molecular analysis of the PK-LR gene revealed the presence of a novel homozygote missense mutation (c.581G>C, p.Arg194Pro). The mutant enzyme displayed heat instability. In addition, we analyzed bilirubin uridine diphosphate (UDP)-glucuronosyltransferase 1A1 gene that revealed a heterozygous state ([TA]6/[TA]7). After a clear diagnosis of PK deficiency, the patient underwent splenectomy.

PMID:
29309376
DOI:
10.1097/MPH.0000000000001073
[Indexed for MEDLINE]

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