Glucose-6-phosphate dehydrogenase deficiency induced hemolytic anemia and methemoglobinemia: a case report in a 7 -year-old female patient

Abstract Background Patients affected by glucose-6-phosphate dehydrogenase (G6PDH) deficiency are often asymptomatic until an oxidative stress occurs, causing acute hemolytic anemia. The coexistence of hemolytic crisis secondary to G6PDH deficiency and methemoglobinemia is an already known phenomeno...

Full description

Saved in:
Bibliographic Details
Main Authors: Adalgisa Fastuca, Antonio Vergori, Giuseppe Robustelli, Chiara Piccolo, Maria Ragazzo, Maddalena Marinoni, Massimo Agosti
Format: Article
Language:English
Published: BMC 2025-08-01
Series:Italian Journal of Pediatrics
Subjects:
Online Access:https://doi.org/10.1186/s13052-025-02051-2
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1849226054436126720
author Adalgisa Fastuca
Antonio Vergori
Giuseppe Robustelli
Chiara Piccolo
Maria Ragazzo
Maddalena Marinoni
Massimo Agosti
author_facet Adalgisa Fastuca
Antonio Vergori
Giuseppe Robustelli
Chiara Piccolo
Maria Ragazzo
Maddalena Marinoni
Massimo Agosti
author_sort Adalgisa Fastuca
collection DOAJ
description Abstract Background Patients affected by glucose-6-phosphate dehydrogenase (G6PDH) deficiency are often asymptomatic until an oxidative stress occurs, causing acute hemolytic anemia. The coexistence of hemolytic crisis secondary to G6PDH deficiency and methemoglobinemia is an already known phenomenon, especially after the ingestion of fava beans. While past literature described this association primarily in adult patients, it remains an unusual finding in pediatric population. Our patient's age, as long as her gender, and a negative family history represent, indeed, the peculiarity of what we described. Case presentation We present the case of a 7-year-old female patient with a clinical history of hyperpyrexia, several episodes of yellowish vomit, hypercromic urine, loose stools, asthenia with jaundice. At home paracetamol and a single dose of ibuprofen were administered. No recent history of fava bean ingestion or relevant events were reported in physiological and pathological anamnesis. Family history was negative for hematological comorbidities. Blood tests performed at the emergency room showed a picture of severe anemia with negative direct and indirect Coombs tests, mild acute renal failure, increased inflammation markers and a methemoglobin level equal to 13.7% on blood gas analysis. The detection of vital parameters showed O2-Sat equal to 75% without signs of respiratory distress. A broad-spectrum antibiotic therapy with ceftriaxone and oxygen-therapy were administered, hospitalization was then arranged. Immune-mediated anemia and lymphoproliferative diseases were excluded. G6PDH dosage was requested, resulting indicative of deficiency. Fecal virus testing revealed a positivity for Norovirus. Transfusions of red cell concentrates (RCC) were performed, and the methemoglobin value gradually decreased with stabilization of the hemoglobin, so that methylene blue therapy was not administrated. The patient’s clinical conditions improved in almost 5 days. Conclusions When G6PDH deficiency and methemoglobinemia coexist, a prompt diagnosis is essential. The administration of methylene blue, therapy of choice for the treatment of methemoglobinemia, in fact, may cause a worsening of hemolytic crises in patients affected by G6PDH deficiency. Considering our patient’s clinical features, not clearly evocative of G6PDH deficiency, this case represented a challenge for both diagnosis and treatment, reminding to always consider G6PDH deficiency in case of hemolytic anemia associated with methemoglobinemia.
format Article
id doaj-art-3ad8ef51129d4aa6a3e7a06bbbd48688
institution Kabale University
issn 1824-7288
language English
publishDate 2025-08-01
publisher BMC
record_format Article
series Italian Journal of Pediatrics
spelling doaj-art-3ad8ef51129d4aa6a3e7a06bbbd486882025-08-24T11:41:35ZengBMCItalian Journal of Pediatrics1824-72882025-08-015111810.1186/s13052-025-02051-2Glucose-6-phosphate dehydrogenase deficiency induced hemolytic anemia and methemoglobinemia: a case report in a 7 -year-old female patientAdalgisa Fastuca0Antonio Vergori1Giuseppe Robustelli2Chiara Piccolo3Maria Ragazzo4Maddalena Marinoni5Massimo Agosti6University of InsubriaPediatric Unit, Maternal and Child Department, “F. Del Ponte” HospitalPediatric Oncoematology Unit, “F. Del Ponte” HospitalPediatric Oncoematology Unit, “F. Del Ponte” HospitalPediatric Oncoematology Unit, “F. Del Ponte” HospitalPediatric Oncoematology Unit, “F. Del Ponte” HospitalUniversity of InsubriaAbstract Background Patients affected by glucose-6-phosphate dehydrogenase (G6PDH) deficiency are often asymptomatic until an oxidative stress occurs, causing acute hemolytic anemia. The coexistence of hemolytic crisis secondary to G6PDH deficiency and methemoglobinemia is an already known phenomenon, especially after the ingestion of fava beans. While past literature described this association primarily in adult patients, it remains an unusual finding in pediatric population. Our patient's age, as long as her gender, and a negative family history represent, indeed, the peculiarity of what we described. Case presentation We present the case of a 7-year-old female patient with a clinical history of hyperpyrexia, several episodes of yellowish vomit, hypercromic urine, loose stools, asthenia with jaundice. At home paracetamol and a single dose of ibuprofen were administered. No recent history of fava bean ingestion or relevant events were reported in physiological and pathological anamnesis. Family history was negative for hematological comorbidities. Blood tests performed at the emergency room showed a picture of severe anemia with negative direct and indirect Coombs tests, mild acute renal failure, increased inflammation markers and a methemoglobin level equal to 13.7% on blood gas analysis. The detection of vital parameters showed O2-Sat equal to 75% without signs of respiratory distress. A broad-spectrum antibiotic therapy with ceftriaxone and oxygen-therapy were administered, hospitalization was then arranged. Immune-mediated anemia and lymphoproliferative diseases were excluded. G6PDH dosage was requested, resulting indicative of deficiency. Fecal virus testing revealed a positivity for Norovirus. Transfusions of red cell concentrates (RCC) were performed, and the methemoglobin value gradually decreased with stabilization of the hemoglobin, so that methylene blue therapy was not administrated. The patient’s clinical conditions improved in almost 5 days. Conclusions When G6PDH deficiency and methemoglobinemia coexist, a prompt diagnosis is essential. The administration of methylene blue, therapy of choice for the treatment of methemoglobinemia, in fact, may cause a worsening of hemolytic crises in patients affected by G6PDH deficiency. Considering our patient’s clinical features, not clearly evocative of G6PDH deficiency, this case represented a challenge for both diagnosis and treatment, reminding to always consider G6PDH deficiency in case of hemolytic anemia associated with methemoglobinemia.https://doi.org/10.1186/s13052-025-02051-2Case reportHemolytic anemiaGlucose-6-phosphate dehydrogenase (G6PDH) deficiencyMethemoglobinemiaChild
spellingShingle Adalgisa Fastuca
Antonio Vergori
Giuseppe Robustelli
Chiara Piccolo
Maria Ragazzo
Maddalena Marinoni
Massimo Agosti
Glucose-6-phosphate dehydrogenase deficiency induced hemolytic anemia and methemoglobinemia: a case report in a 7 -year-old female patient
Italian Journal of Pediatrics
Case report
Hemolytic anemia
Glucose-6-phosphate dehydrogenase (G6PDH) deficiency
Methemoglobinemia
Child
title Glucose-6-phosphate dehydrogenase deficiency induced hemolytic anemia and methemoglobinemia: a case report in a 7 -year-old female patient
title_full Glucose-6-phosphate dehydrogenase deficiency induced hemolytic anemia and methemoglobinemia: a case report in a 7 -year-old female patient
title_fullStr Glucose-6-phosphate dehydrogenase deficiency induced hemolytic anemia and methemoglobinemia: a case report in a 7 -year-old female patient
title_full_unstemmed Glucose-6-phosphate dehydrogenase deficiency induced hemolytic anemia and methemoglobinemia: a case report in a 7 -year-old female patient
title_short Glucose-6-phosphate dehydrogenase deficiency induced hemolytic anemia and methemoglobinemia: a case report in a 7 -year-old female patient
title_sort glucose 6 phosphate dehydrogenase deficiency induced hemolytic anemia and methemoglobinemia a case report in a 7 year old female patient
topic Case report
Hemolytic anemia
Glucose-6-phosphate dehydrogenase (G6PDH) deficiency
Methemoglobinemia
Child
url https://doi.org/10.1186/s13052-025-02051-2
work_keys_str_mv AT adalgisafastuca glucose6phosphatedehydrogenasedeficiencyinducedhemolyticanemiaandmethemoglobinemiaacasereportina7yearoldfemalepatient
AT antoniovergori glucose6phosphatedehydrogenasedeficiencyinducedhemolyticanemiaandmethemoglobinemiaacasereportina7yearoldfemalepatient
AT giusepperobustelli glucose6phosphatedehydrogenasedeficiencyinducedhemolyticanemiaandmethemoglobinemiaacasereportina7yearoldfemalepatient
AT chiarapiccolo glucose6phosphatedehydrogenasedeficiencyinducedhemolyticanemiaandmethemoglobinemiaacasereportina7yearoldfemalepatient
AT mariaragazzo glucose6phosphatedehydrogenasedeficiencyinducedhemolyticanemiaandmethemoglobinemiaacasereportina7yearoldfemalepatient
AT maddalenamarinoni glucose6phosphatedehydrogenasedeficiencyinducedhemolyticanemiaandmethemoglobinemiaacasereportina7yearoldfemalepatient
AT massimoagosti glucose6phosphatedehydrogenasedeficiencyinducedhemolyticanemiaandmethemoglobinemiaacasereportina7yearoldfemalepatient