A Diagnostic Dilemma: What Not to Miss in Methaemoglobinaemia

Methaemoglobinaemia is a rare disorder in which haemoglobin loses its ability to deliver oxygen to tissues due to oxidation of haem iron. It may be congenital or acquired, most commonly secondary to medication. Patients present with apparent hypoxia unresponsive to oxygen therapy, which can be life-threatening at higher levels. Here we describe a case of dapsone-induced methaemoglobinaemia, which was initially overlooked due to possible sinister pathologies, leading to extensive investigations and repeated admissions, underscoring the importance of careful ABG interpretation and medication review.

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Publication Details

Journal
Cureus
Published
2025-11-16
DOI
https://doi.org/10.7759/cureus.96966
Citations
1
Primary Topic
Methemoglobinemia and Tumor Lysis Syndrome
Type
article
Field-Weighted Citation Impact
1.52
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article

A Diagnostic Dilemma: What Not to Miss in Methaemoglobinaemia

Adil Javed, Muhammad Masood Hassan, Monowara Rahman Shipi, Muhammad Mohsin Isar et al.
1 citations
Cureus
Methemoglobinemia and Tumor Lysis Syndrome
1.52
article

A Diagnostic Dilemma: What Not to Miss in Methaemoglobinaemia

Adil Javed, Muhammad Masood Hassan, Monowara Rahman Shipi, Muhammad Mohsin Isar, Harshvardhan P Thakar
article en
1 citations

Abstract

Methaemoglobinaemia is a rare disorder in which haemoglobin loses its ability to deliver oxygen to tissues due to oxidation of haem iron. It may be congenital or acquired, most commonly secondary to medication. Patients present with apparent hypoxia unresponsive to oxygen therapy, which can be life-threatening at higher levels. Here we describe a case of dapsone-induced methaemoglobinaemia, which was initially overlooked due to possible sinister pathologies, leading to extensive investigations and repeated admissions, underscoring the importance of careful ABG interpretation and medication review.

CureusVol. 17(11)
United Lincolnshire Hospitals NHS Trust (GB)
Openalex Percentile: Top 13%
Methemoglobinemia and Tumor Lysis Syndrome
1.52
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