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DOI 10.1136/bcr-2025-266921

Медицинская библиотека · BMJ case reports · 2026

The blue dilemma: a rare presentation of dual hemoglobinopathy in a pregnant patient.

Thakur Krishma, Satodiya Mohit, Pandher Dilpreet Kaur, Takkar Navneet

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Аннотация

Methaemoglobinaemia is a rare disorder due to an increase in the amount of a variant of haemoglobin known as methaemoglobin (MetHb), which decreases the oxygen-carrying capacity of blood. It is usually caused by enzyme deficiency. Hb Q India is another rare alpha-chain variant haemoglobinopathy. A young primigravida was referred due to low oxygen saturation. She was otherwise asymptomatic. Patient was received with peripheral cyanosis and in a tachypneic state due to advanced labour. On the pulse oximeter, oxygen saturation was found to be 40%; hence, the patient was immediately intubated, and instrumental delivery was conducted. A detailed workup showed high MetHb levels, and the Hb Q India variant was detected on HPLC. We present this case report of dual haemoglobinopathy, which can pose a great diagnostic dilemma.Methaemoglobinaemia is usually an asymptomatic disease and is managed conservatively, but if symptomatic, it requires intensive management to avoid fatality.

Для цитирования: Thakur Krishma, Satodiya Mohit, Pandher Dilpreet Kaur, Takkar Navneet. The blue dilemma: a rare presentation of dual hemoglobinopathy in a pregnant patient.. BMJ case reports. 2026. DOI: 10.1136/bcr-2025-266921.

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