A Rare Case of CML Presenting with Isolated Thrombocytosis

Chronic myeloid leukemia (CML) is a hematological malignancy characterized by uncontrolled granulocyte proliferation driven by the BCR-ABL mutation. Typically, CML presents with leukocytosis, anemia, and splenomegaly. 1 Thrombocytopenia or thrombocytosis may also occur, although isolated platelet abnormalities are uncommon as an initial presentation. In this case report, we present a rare case of a woman in her 50s who initially presented with metabolic encephalopathy and isolated thrombocytosis. Despite thorough investigation for essential thrombocytosis, looking for the most common mutations in ET, such as JAK2 or calreticulin 2, the etiology of her thrombocytosis remained unexplained. It was only upon the subsequent development of leukocytosis and anemia that further investigation led to the diagnosis of CML.

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Publication Details

Journal
Advances in Clinical Medical Research and Healthcare Delivery
Published
2024-11-04
DOI
https://doi.org/10.53785/2769-2779.1250
Primary Topic
Chronic Myeloid Leukemia Treatments
Type
article
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article

A Rare Case of CML Presenting with Isolated Thrombocytosis

Himal Kharel, Aditya Sanjeevi, Daniel Idoate Jose Domench, Aniket Rao et al.
Advances in Clinical Medical Research and Healthcare Delivery
Chronic Myeloid Leukemia Treatments
article

A Rare Case of CML Presenting with Isolated Thrombocytosis

Himal Kharel, Aditya Sanjeevi, Daniel Idoate Jose Domench, Aniket Rao, Gaby Razzouk
article en

Abstract

Chronic myeloid leukemia (CML) is a hematological malignancy characterized by uncontrolled granulocyte proliferation driven by the BCR-ABL mutation. Typically, CML presents with leukocytosis, anemia, and splenomegaly. 1 Thrombocytopenia or thrombocytosis may also occur, although isolated platelet abnormalities are uncommon as an initial presentation. In this case report, we present a rare case of a woman in her 50s who initially presented with metabolic encephalopathy and isolated thrombocytosis. Despite thorough investigation for essential thrombocytosis, looking for the most common mutations in ET, such as JAK2 or calreticulin 2, the etiology of her thrombocytosis remained unexplained. It was only upon the subsequent development of leukocytosis and anemia that further investigation led to the diagnosis of CML.

Advances in Clinical Medical Research and Healthcare DeliveryVol. 4(4)
Openalex Percentile: Top 67%
Chronic Myeloid Leukemia Treatments
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