Meeting Abstracts

Published: Aug 04, 2026 | DOI: 10.24911/SJEMed.12-2558

 KID THAT DO METH CASE REPORT ON PEDIATRIC METHHEMOGLOBINEMIA


Authors: DR. SIFRAH ISAAC COTTADIYEL , DR. NITIN JAGASIA


Abstract

Methemoglobinemia is a rare but life-threatening hematologic condition where hemoglobin is oxidized from the ferrous (Fe2+) to the ferric (Fe3+) state, impairing oxygen delivery to tissues. While congenital forms exist, acquired methemoglobinemia often triggered by medications or chemical exposures is more common. Prevalence in pediatric populations is estimated at approximately 0.0015%. ​

Case Presentation: A 6-year-old male presented to the Apollo Hospitals Emergency Department with fever, abdominal pain, vomiting, epistaxis, and acute breathlessness. Physical examination revealed central and peripheral cyanosis with an SpO2 of 88% on room air, which only improved to 92% despite high-flow oxygen (10L). Notably, the patient had a history of exposure to a watch repair solution and prior consumption of "outside food." ​

Diagnostic Workup: Venous Blood Gas (VBG) analysis confirmed methemoglobinemia with a level (FMetHb) of 31.0% and respiratory alkalosis. Laboratory results showed mild thrombocytopenia (Platelets: 89,000) and a normal hemoglobin (15.5 g/dL). G6PD deficiency was ruled out. Despite initial chest X-ray findings suggesting cardiomegaly, 2D echocardiography with contrast confirmed normal cardiac function and no pulmonary arteriovenous malformations.

 ​Management and Outcome: The primary objective was to restore oxygen-carrying capacity. The patient received a 1 mg/kg IV bolus of Methylene Blue (20 mg diluted in 0.9% NS) over 15 minutes, alongside Vitamin C (500 mg BD) and supportive oxygen. Following the antidote, SpO2 improved to 100%, and cyanosis resolved. Post-treatment VBG showed FMetHb reduced to 6.1%. The patient remained hemodynamically stable and was successfully weaned from oxygen.

 ​Discussion: This case highlights the "saturation gap" low SpO2 unresponsive to supplemental oxygen as a clinical hallmark of methemoglobinemia. Prompt administration of Methylene Blue is the gold standard for levels >20% or symptomatic patients. ​

Conclusion: Early recognition of environmental toxins is critical for diagnosis. Management must focus on rapid reversal with Methylene Blue and comprehensive patient counseling to prevent re-exposure to oxidizing agents. In refractory cases, escalation to exchange transfusion or hyperbaric oxygen may be necessary.


Keywords: METHHEMOGLOBINEMIA



Pubmed Style

DR. SIFRAH ISAAC COTTADIYEL, DR. NITIN JAGASIA.  KID THAT DO METH CASE REPORT ON PEDIATRIC METHHEMOGLOBINEMIA. SJE Med. 2026; 04 (August 2026): -. doi:10.24911/SJEMed.12-2558

Publication History

Received: January 29, 2026

Accepted: April 13, 2026

Published: August 04, 2026


Authors

DR. SIFRAH ISAAC COTTADIYEL

APOLLO HOSPITAL, NAVI MUMBAI

DR. NITIN JAGASIA

APOLLO HOSPITALS, NAVI MUMBAI