Successful Resolution of Compartment Syndrome in a Pediatric Patient With B-cell Acute Lymphoblastic Leukemia

We report a case of a 17-year-old male presenting with acute compartment syndrome (CS) of the lower extremity as the initial manifestation of CRLF2-positive, Ph-like B-cell acute lymphoblastic leukemia (B-ALL), without evidence of leukemic infiltration or hematoma. Emergent fasciotomy was performed, followed by cytoreduction with hydroxyurea to allow wound healing before induction chemotherapy. The patient fully recovered and completed induction without complications. This case highlights the importance of recognizing CS as a rare presenting feature of leukemia, and supports hydroxyurea bridging as a viable strategy when immediate chemotherapy is contraindicated to support surgical recovery.

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Publication Details

Journal
Journal of Pediatric Hematology/Oncology
Published
2025-12-12
DOI
https://doi.org/10.1097/mph.0000000000003149
Primary Topic
Muscle and Compartmental Disorders
Type
article
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article

Successful Resolution of Compartment Syndrome in a Pediatric Patient With B-cell Acute Lymphoblastic Leukemia

Dell McLaughlin, Dana Olszewski, Bailey J. Ross, Daniel S. Wechsler et al.
Journal of Pediatric Hematology/Oncology
Muscle and Compartmental Disorders
article

Successful Resolution of Compartment Syndrome in a Pediatric Patient With B-cell Acute Lymphoblastic Leukemia

Dell McLaughlin, Dana Olszewski, Bailey J. Ross, Daniel S. Wechsler, Tyler Vajdic, Peter M. Carlson, Michael Busch
article en

Abstract

We report a case of a 17-year-old male presenting with acute compartment syndrome (CS) of the lower extremity as the initial manifestation of CRLF2-positive, Ph-like B-cell acute lymphoblastic leukemia (B-ALL), without evidence of leukemic infiltration or hematoma. Emergent fasciotomy was performed, followed by cytoreduction with hydroxyurea to allow wound healing before induction chemotherapy. The patient fully recovered and completed induction without complications. This case highlights the importance of recognizing CS as a rare presenting feature of leukemia, and supports hydroxyurea bridging as a viable strategy when immediate chemotherapy is contraindicated to support surgical recovery.

Journal of Pediatric Hematology/OncologyVol. 48(1)
Emory University (US), Aflac (United States) (US), Children's Healthcare of Atlanta (US)
Good health and well-being
Openalex Percentile: Top 25%
Muscle and Compartmental Disorders
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