Evidence map›Paper›PMID 40329513›Full record

ArticleThe American journal of case reports2025

A Rare Case of Hypoxia and Cyanosis Secondary to Multifactorial Medication-Induced Sulfhemoglobinemia.

Megan M Mansour, Robert M Seby, Aya Elalfy, Mario El Hayek, Tuhama S Rihani, Edson J Mwakyanjala, Libardo Rueda Prada

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Article in The American journal of case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

7 authors.

Megan M MansourDepartment of Internal Medicine, Mayo Clinic, Jacksonville, FL, USA.
Robert M SebyDepartment of Internal Medicine, Mayo Clinic, Jacksonville, FL, USA.
Aya ElalfyDepartment of Internal Medicine, Mayo Clinic, Jacksonville, FL, USA.
Mario El HayekDepartment of Internal Medicine, Mayo Clinic, Jackssonville, FL, USA.
Tuhama S RihaniMayo Clinic College of Medicine and Science, Rochester, MN, USA.
Edson J MwakyanjalaMayo Clinic College of Medicine and Science, Rochester, MN, USA.
Libardo Rueda PradaMayo Clinic College of Medicine and Science, Rochester, MN, USA.ORCID 0000-0001-6964-5956

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Fatigue and dyspnea, especially with hypoxia, are common in acute care and can indicate various conditions. Sulfhemoglobinemia is a rare but important consideration when a large saturation gap is present, as most blood gas analyzers do not detect it. Medication exposure, particularly to phenazopyridine and other oxidant drugs, is a leading cause. Early recognition of this diagnosis is crucial, as recurrence is likely with re-exposure to the precipitating agent. CASE REPORT A 37-year-old woman presented with acute dyspnea, lethargy, and hypoxia after exposure to severe oxidizing agents, including first-time use of trimethoprim-sulfamethoxazole and phenazopyridine, as well as lidocaine during a recent dental procedure (not her first exposure). Shortly thereafter, she developed tachycardia, tachypnea, and hypoxia, with concurrent hemolytic anemia. Despite oxygen therapy, she had a persistent elevated saturation gap. Arterial blood gas confirmed dyshemoglobinemia, and further testing identified sulfhemoglobinemia (1.3%). She was treated with blood transfusion and discontinuation of oxidizing agents to prevent further hypoxia. CONCLUSIONS Sulfhemoglobinemia is a rare and often missed diagnosis, as most blood gases analyzers do not measure sulfhemoglobin. Despite this, this diagnosis requires great clinical suspicion, as patients are at high risk for repeated exposure to offending agents and recurrence of life-threatening hypoxia.

Indexed as

CyanosisHypoxiaPhenazopyridineAdultFemaleHumansPhenazopyridine

Identifiers

PMID40329513
PMCPMC12067997

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