An Exceptional Case of Cobalamin Deficiency that Presented with Extremely High Indirect Bilirubin Levels

Authors

  • Hamza Kaya Abant Izzet Baysal University Hospital, Department of Internal Medicine, Bolu, Turkey.
  • Tuba Taslamacioglu Duman Abant Izzet Baysal University Hospital, Department of Internal Medicine, Bolu, Turkey.
  • Gizem Kahveci Abant Izzet Baysal University Hospital, Department of Internal Medicine, Bolu, Turkey.
  • Elif Basaran Abant Izzet Baysal University Hospital, Department of Internal Medicine, Bolu, Turkey.
  • Gulali Aktas Abant Izzet Baysal University Hospital, Department of Internal Medicine, Bolu, Turkey.

Abstract

Cobalamin deficiency anemia is a type of anemia that present with weakness, fatigue, icteric sclera and neuropathy. Main causes of
cobalamin deficiency are low intake or decreased absorption (gastric and intestinal causes). In present case, we report a 65-year-old male who
presented to the emergency department with signs and symptoms of cobalamin deficiency including bilateral peripheral neuropathy, icteric skin
and sclera, and abdominal pain in right upper quadrant. He had low cobalamin and extremely high bilirubin levels (8mg/dL) in serum. After
the diagnosis of cobalamin deficiency established, 1mg daily cobalamin treatment initiated for five days which would follow weekly and
monthly intramuscular injections consequently. Hemolysis and other causes of elevated indirect bilirubin levels were excluded in differential
diagnosis. Clinical and laboratory improvements were achieved after the treatment. In conclusion, physicians should kept in mind cobalamin
deficiency even in subjects with unusual high levels of indirect bilirubin.

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Published

2022-06-30

How to Cite

1.
Kaya H, Duman TT, Kahveci G, Basaran E, Aktas G. An Exceptional Case of Cobalamin Deficiency that Presented with Extremely High Indirect Bilirubin Levels. Nat J Health Sci [Internet]. 2022Jun.30 [cited 2024Apr.26];7(2):96-7. Available from: https://ojs.njhsciences.com/index.php/njhs/article/view/316

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Section

Case Report

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