Congenital methaemoglobinaemia in a 61-year-old patient with normal haemoglobin levels.

Neth J Med

Department of Internal Medicine, Academic Medical Center, University of Amsterdam, Amsterdam, the Netherlands.

Published: May 2018

A 61-year-old Ghanaian woman presented with dizziness and low oxygen saturations whereupon a methaemoglobin level of 24.9% was obtained. Initially it was thought to be caused by an unknown toxin. However, failure to normalise spontaneously and a short recurrence following administration of methylene blue suggested a congenital cause. Subsequently a novel variant in the CYB5R3 gene, coding for Cytochrome b5 reductase, was demonstrated. Absence of polycythaemia prompted additional analysis for a concomitant haemoglobinopathy.

Download full-text PDF

Source

Publication Analysis

Top Keywords

congenital methaemoglobinaemia
4
methaemoglobinaemia 61-year-old
4
61-year-old patient
4
patient normal
4
normal haemoglobin
4
haemoglobin levels
4
levels 61-year-old
4
61-year-old ghanaian
4
ghanaian woman
4
woman presented
4

Similar Publications

Methemoglobinemia is a rare but potentially life-threatening condition in which hemoglobin is oxidized, impairing the oxygen-carrying capacity. While congenital forms exist, acquired methemoglobinemia can occur in perioperative settings, especially following exposure to oxidizing agents such as dyes used in sentinel lymph node biopsy (SLNB). Patent Blue V, a synthetic aniline dye commonly used for SLNB, has been associated with rare but serious adverse effects, including methemoglobinemia.

View Article and Find Full Text PDF

Life-Threatening Methaemoglobinaemia Secondary to Cetrimide.

Eur J Case Rep Intern Med

September 2024

Department of Medicine, Division of Pulmonary and Critical Care Medicine, Mount Lebanon Hospital Balamand University Medical Center, Beirut, Lebanon.

Article Synopsis
  • * The condition is characterized by oxidized hemoglobin (ferric state), leading to symptoms like low blood oxygen levels, hypoxia, and distinct chocolate-colored blood.
  • * A case study highlights how cetrimide, used in abdominal surgeries for hydatid cysts, can trigger severe methaemoglobinaemia, which often goes undiagnosed but has a high risk of mortality.
View Article and Find Full Text PDF
Article Synopsis
  • - Methemoglobinemia is a condition where hemoglobin is oxidized, preventing it from binding oxygen, leading to symptoms like cyanosis and potential heart failure; it can be congenital or acquired, with the congenital form being rare.
  • - A case study of a 22-year-old man with congenital methemoglobinemia demonstrated the need for careful perioperative management during dental surgery, including avoiding certain anesthetics and ensuring appropriate oxygenation levels.
  • - Effective management of congenital methemoglobinemia during surgery requires preoperative assessment, multidisciplinary care, avoidance of oxidizing agents, and strategies to maintain the patient's oxygenation and cardiovascular stability.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!