Concurrent intracranial hemorrhage and spontaneous tumor Lysis syndrome as the initial presentation of KMT2A::AFF1-rearranged adult ALL: a case report

Background: -rearranged ALL is a high-risk subtype with an aggressive course. However, the simultaneous occurrence of catastrophic intracranial hemorrhage (ICH) and spontaneous tumor lysis syndrome (TLS) as the initial presentation is rare in adult patients and remains poorly characterized in the literature. Case Presentation: fusion gene. Conclusion: -rearranged ALL, characterized by the concurrent development of ICH and spontaneous TLS prior to the initiation of any leukemia-specific therapy. It underscores the critical importance of promptly recognizing this hyperacute syndrome in young patients presenting with unexplained neurological symptoms and profound hematologic abnormalities. Early multidisciplinary management and awareness of high-risk genetic profiles are essential, although the prognosis in such scenarios remains exceedingly poor.

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Publication Details

Journal
Frontiers in Oncology
Published
2026-04-21
DOI
https://doi.org/10.3389/fonc.2026.1716717
Primary Topic
Methemoglobinemia and Tumor Lysis Syndrome
Type
article
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article

Concurrent intracranial hemorrhage and spontaneous tumor Lysis syndrome as the initial presentation of KMT2A::AFF1-rearranged adult ALL: a case report

Rongguo Wei, Min Wei, 賴妤宜, Ligang Zhao
Frontiers in Oncology
Methemoglobinemia and Tumor Lysis Syndrome
article

Concurrent intracranial hemorrhage and spontaneous tumor Lysis syndrome as the initial presentation of KMT2A::AFF1-rearranged adult ALL: a case report

Rongguo Wei, Min Wei, 賴妤宜, Ligang Zhao
article en

Abstract

Background: -rearranged ALL is a high-risk subtype with an aggressive course. However, the simultaneous occurrence of catastrophic intracranial hemorrhage (ICH) and spontaneous tumor lysis syndrome (TLS) as the initial presentation is rare in adult patients and remains poorly characterized in the literature. Case Presentation: fusion gene. Conclusion: -rearranged ALL, characterized by the concurrent development of ICH and spontaneous TLS prior to the initiation of any leukemia-specific therapy. It underscores the critical importance of promptly recognizing this hyperacute syndrome in young patients presenting with unexplained neurological symptoms and profound hematologic abnormalities. Early multidisciplinary management and awareness of high-risk genetic profiles are essential, although the prognosis in such scenarios remains exceedingly poor.

Frontiers in OncologyVol. 16
Xinjiang Medical University (CN), Fifth Affiliated Hospital of Xinjiang Medical University (CN), First People's Hospital of Nanning (CN)
Good health and well-being
Openalex Percentile: Top 20%
Methemoglobinemia and Tumor Lysis Syndrome
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