Case report of congenital methemoglobinemia: an uncommon cause of neonatal cyanosis

Background Methemoglobinemia can be an acquired or congenital condition. The acquired form occurs from exposure to oxidative agents. Congenital methemoglobinemia is a rare and potentially life-threatening cause of cyanosis in newborns that can be caused by either cytochrome $ B_{5} $ reductase or he...
Ausführliche Beschreibung

Background Methemoglobinemia can be an acquired or congenital condition. The acquired form occurs from exposure to oxidative agents. Congenital methemoglobinemia is a rare and potentially life-threatening cause of cyanosis in newborns that can be caused by either cytochrome $ B_{5} $ reductase or hemoglobin variants known as Hemoglobin M. Case presentation A term male infant developed cyanosis and hypoxia shortly after birth after an uncomplicated pregnancy, with oxygen saturations persistently 70–80% despite 1.0 FiO2 and respiratory support of CPAP+ 6 cm H2O. Pre- and post-ductal saturations were equal and remained below 85%. Initial radiographic and echography imaging was normal. Capillary blood gas values were reassuring with normal pH and an elevated pO2. Investigations to rule out hemolysis and end-organ dysfunction were within acceptable range. Given the absence of clear cardiac or pulmonary etiology of persistent cyanosis, hematologic causes such as methemoglobinemia were explored. No family history was available at the time of transfer to our institution. Unconjugated hyperbilirubinemia > 5 mg/dL (442 μmol/L) interfered with laboratory equipment measurement, making accurate methemoglobin levels unattainable despite multiple attempts. Initial treatment with methylene blue or ascorbic acid was considered. However, upon arrival of the presumed biological father, a thorough history revealed an extensive paternal family history of neonatal cyanosis due to a rare mutation resulting in a hemoglobin M variant. Given this new information, hematology recommended supportive care as well as further testing to confirm the diagnosis of congenital methemoglobinopathy. Whole genome sequencing revealed a likely pathogenic variation in hemoglobin. The neonate was discharged home at 2 weeks of age on full oral feeds with 0.25 L/min nasal cannula as respiratory support, with close outpatient follow-up. By 5 weeks of age, he was weaned off respiratory support. Conclusion Congenital methemoglobinemia should be considered in the differential diagnosis for newborns with persistent hypoxemia despite normal imaging and laboratory values. Accurate quantification of methemoglobin concentrations is challenging in neonates due to the presence of other substances that absorb light at similar wavelengths, including HbF, bilirubin, and lipids. Ausführliche Beschreibung

Autor*in:	Lyle, Allison N. J. [verfasserIn] Spurr, Rebecca Kirkey, Danielle Albert, Catherine M. Billimoria, Zeenia Perez, Jose Puia-Dumitrescu, Mihai

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2022

Schlagwörter:	Congenital methemoglobinemia Neonatal Case report Hemoglobin M Fort Ripley

Anmerkung:	© The Author(s) 2022

Übergeordnetes Werk:	Enthalten in: Maternal health, neonatology and perinatology - London : BioMed Central, 2015, 8(2022), 1 vom: 16. Sept.
Übergeordnetes Werk:	volume:8 ; year:2022 ; number:1 ; day:16 ; month:09

Links:	Volltext

DOI / URN:	10.1186/s40748-022-00142-0

Katalog-ID:	SPR050998544