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Patient with clinical celiac disease mimicking triple-negative essential thrombocythemia. | LitMetric

Patient with clinical celiac disease mimicking triple-negative essential thrombocythemia.

Clin Case Rep

Department of Hematology and Oncology Hamad Medical Corporation Doha Qatar.

Published: April 2022

AI Article Synopsis

  • * Essential thrombocythemia patients often have mutations affecting blood cell production, but around 10%-15% are considered “triple-negative,” meaning no mutations are detected.
  • * A case is presented of a young patient diagnosed as triple-negative ET who was found to have celiac disease, highlighting the importance of screening for celiac disease in such patients before moving on to pricier tests.

Article Abstract

Platelets are acute-phase reactants, which can be elevated due to a secondary cause or less commonly because of a primary mechanism. Primary disorders include hematological conditions such as myelodysplastic syndrome, acute myeloid leukemia, chronic myeloid leukemia, polycythemia vera, and essential thrombocythemia (ET). Most ET patients have a mutation in the genes regulating thrombopoiesis, , , or genes. But 10%-15% of ET patients are triple-negative, where patients have no detectable mutation. We report a young patient with no significant past medical history evaluated for persistent thrombocytosis. She was initially diagnosed as triple-negative ET based on a bone marrow biopsy. She had positive antibodies for celiac disease, and the diagnosis was confirmed by a small bowel biopsy, which is confirmatory for diagnosing celiac disease in adults. We recommend screening triple-negative ET patients for celiac disease before going to more expensive tests.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8989016PMC
http://dx.doi.org/10.1002/ccr3.5197DOI Listing

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