A Rare Case of Recurrent Spontaneous Soft Tissue Hematomas in Chronic Myeloid Leukemia (CML) – Case Report

Chronic myeloid leukemia (CML) is a myeloproliferative neoplasm characterized by the Philadelphia chromosome, BCR–ABL1 fusion gene. Although bleeding manifestations are recognized, spontaneous soft-tissue hematomas are rare. We report a 21-year-old male with chronic-phase CML who developed recurrent spontaneous intramuscular hematomas in the absence of trauma. He presented with hyperleukocytosis and a gluteal hematoma complicated by compartment syndrome requiring surgical decompression. In the absence of identifiable coagulation abnormalities, a multifactorial mechanism, including hyperleukocytosis-associated microvascular dysfunction and possible qualitative platelet abnormalities, may have contributed. This case highlights an uncommon but serious complication of uncontrolled CML.

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Journal
SN Comprehensive Clinical Medicine
Published
2026-11-06
DOI
https://doi.org/10.1007/s42399-026-02548-9
Primary Topic
Case Reports on Hematomas
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article
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A Rare Case of Recurrent Spontaneous Soft Tissue Hematomas in Chronic Myeloid Leukemia (CML) – Case Report

Amit Keith Correa, Hila Shaim, Monitha Pinnamaneni, Hardik Zinzala et al.
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SN Comprehensive Clinical Medicine
Case Reports on Hematomas
article

A Rare Case of Recurrent Spontaneous Soft Tissue Hematomas in Chronic Myeloid Leukemia (CML) – Case Report

Amit Keith Correa, Hila Shaim, Monitha Pinnamaneni, Hardik Zinzala, Lily Chen, Amitesh Krishna Srinivasan
article en

Abstract

Chronic myeloid leukemia (CML) is a myeloproliferative neoplasm characterized by the Philadelphia chromosome, BCR–ABL1 fusion gene. Although bleeding manifestations are recognized, spontaneous soft-tissue hematomas are rare. We report a 21-year-old male with chronic-phase CML who developed recurrent spontaneous intramuscular hematomas in the absence of trauma. He presented with hyperleukocytosis and a gluteal hematoma complicated by compartment syndrome requiring surgical decompression. In the absence of identifiable coagulation abnormalities, a multifactorial mechanism, including hyperleukocytosis-associated microvascular dysfunction and possible qualitative platelet abnormalities, may have contributed. This case highlights an uncommon but serious complication of uncontrolled CML.

SN Comprehensive Clinical MedicineVol. 8(1)
Lyndon Baines Johnson Hospital (US)
Good health and well-being
Openalex Percentile: Top 12%
Case Reports on Hematomas
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