Abstract
Methemoglobin is an oxidized form of hemoglobin. NADH methemoglobin reductase deficiency or inactivity is the cause of methemoglobin. Excessive production, resulting in accumulation, causes methemoglobinemia. It can be congenital or acquired. We present a case of dormant congenital methemoglobinemia detected accidentally on preoperative assessment, due to low oxygen saturation even at F1O2-1.0 associated with central cyanosis. The patient had 27.7 % methemoglobin, living his life without any complications. The patient was operated upon successfully for tympanoplasty and mastoidectomy under local anesthesia by taking proper precautions.
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Acknowledgments
We owe thanks and due acknowledgments to Dr. Pryanka for her help in collection of sample and photographs and Mr. Guruswami P, for his technical help in Biochemistry.
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This study is purely a self funded study, approved by the institutional ethical committee.
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The sample used for the study was blood, which was collected from patient after explaining and taking consent.
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Trivedi, D.J., Joshiraj, B., Bidkar, V. et al. Methemoglobinemia: Living with Dormant Devil. Ind J Clin Biochem 32, 248–250 (2017). https://doi.org/10.1007/s12291-016-0586-5
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DOI: https://doi.org/10.1007/s12291-016-0586-5