Ischemic stroke as the initial presentation in acute myeloid leukemia vs. myelodysplastic syndrome: a case report and literature review with pathophysiological and clinical exploration

被引:1
作者
Elshony, Hosna [1 ]
Alzahrani, Meshari [2 ]
Khafaji, Salah [2 ]
Almuhanna, Rakan [2 ]
Khalil, Khalid [3 ]
Mudassir, Rabia [2 ]
机构
[1] Menoufiya Univ, Fac Med, Dept Neuropsychiat, Shibin Al Kawm, Egypt
[2] Secur Forces Hosp, Dept Neurol Internal Med, Almashaer St,Altaif Rd, Mecca, Saudi Arabia
[3] Secur Forces Hosp, Dept Internal Med Hematol, Mecca, Saudi Arabia
关键词
Ischemic stroke; Acute myeloid leukemia (AML); Myelodysplastic syndrome (MDS); THROMBOSIS; RISK; INFARCTION; CANCER;
D O I
10.1007/s10072-024-07367-1
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BackgroundMyelodysplastic syndromes (MDS) and acute myeloid leukemia (AML) present intricate challenges due to their diverse clinical manifestations and thrombotic complications. Thromboembolism (TE) incidence in newly diagnosed AML patients is noteworthy, with arterial TE linked to poorer overall survival. Ischemic strokes, although relatively low in prevalence, carry significant clinical implications.Case descriptionWe report the case of an 84-year-old male with Type 2 Diabetes, Hypertension, and Chronic Kidney Disease, presenting with seizures, focal neurological deficits, and pancytopenia. An unexpected diagnosis of AML or MDS emerged during the investigation. Despite interventions, the patient's condition deteriorated, leading to a fatal outcome weeks later.ConclusionThis case underscores the intricate relationship between hematologic malignancies and ischemic stroke. The rarity of this complication emphasizes the importance of understanding the multifaceted mechanisms at play, including hyperleukocytosis, pro-inflammatory cytokine release, coagulation cascade activation, and direct interactions with endothelial cells. In our literature review, analysis of 15 cases, including ours, revealed a wide age range (3-87 years) and a gender bias towards females. AML diagnosis was predominant, with uniformly low platelet counts. Cortical infarctions, especially in the anterior circulation, were common. Hyperleukocytosis, disseminated intravascular coagulation (DIC), and fatal outcomes were observed in a subset of cases. Despite the grim statistics and often poor prognosis, the identification of specific risk factors, such as thrombocytopenia and cytogenetic abnormalities, offers avenues for targeted prevention and management.
引用
收藏
页码:3297 / 3304
页数:8
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