Clinically suspected central nervous system Richter transformation presenting with progressive psychiatric symptoms: A case report

Abstract Background Central nervous system (CNS) involvement associated with Richter transformation (RT) is a rare complication of chronic lymphocytic leukemia (CLL). Neurological manifestations are heterogeneous. To our knowledge, no previous reports have described CNS RT presenting predominantly with psychiatric and behavioral symptoms. We report a clinically suspected case of CNS RT presenting predominantly with progressive psychiatric symptoms in the presence of extensive CNS lesions but without apparent focal neurological deficits. Case Presentation A 71‐year‐old man with no psychiatric history developed progressive personality change, irritability, emotional lability, behavioral disinhibition, and sleep–wake cycle disturbance. Gadolinium‐enhanced fluid‐attenuated inversion recovery magnetic resonance imaging demonstrated newly developed multifocal lesions predominantly involving the bilateral temporal lobes. Hematological evaluation established previously unrecognized CLL. Although histopathological confirmation was not obtained, the overall clinical, radiological, and laboratory findings supported CNS involvement associated with clinically suspected RT as the most likely diagnosis. Progressive neuropsychiatric deterioration limited invasive diagnostic procedures and disease‐directed treatment. Supportive and palliative management was provided, and the patient died of aspiration pneumonia 114 days after surgery. Conclusion This case demonstrates that clinically suspected CNS RT may present predominantly with progressive psychiatric and behavioral symptoms in the absence of focal neurological deficits. Severe neuropsychiatric symptoms may themselves impede diagnostic confirmation and disease‐directed treatment. When pathological confirmation is not feasible, multidisciplinary discussion and shared decision‐making with the patient and family, together with explicit acknowledgment of diagnostic uncertainty and careful balancing of the benefits and burdens of further investigation and treatment, may support patient‐centered care.

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Journal
Psychiatry and Clinical Neurosciences Reports
Published
2026-10-19
DOI
https://doi.org/10.1002/pcn5.70421
Primary Topic
Chronic Lymphocytic Leukemia Research
Type
article
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article

Clinically suspected central nervous system Richter transformation presenting with progressive psychiatric symptoms: A case report

Yusuke Sugama, 哲朗 石田
Psychiatry and Clinical Neurosciences Reports
Chronic Lymphocytic Leukemia Research
article

Clinically suspected central nervous system Richter transformation presenting with progressive psychiatric symptoms: A case report

Yusuke Sugama, 哲朗 石田
article en

Abstract

Abstract Background Central nervous system (CNS) involvement associated with Richter transformation (RT) is a rare complication of chronic lymphocytic leukemia (CLL). Neurological manifestations are heterogeneous. To our knowledge, no previous reports have described CNS RT presenting predominantly with psychiatric and behavioral symptoms. We report a clinically suspected case of CNS RT presenting predominantly with progressive psychiatric symptoms in the presence of extensive CNS lesions but without apparent focal neurological deficits. Case Presentation A 71‐year‐old man with no psychiatric history developed progressive personality change, irritability, emotional lability, behavioral disinhibition, and sleep–wake cycle disturbance. Gadolinium‐enhanced fluid‐attenuated inversion recovery magnetic resonance imaging demonstrated newly developed multifocal lesions predominantly involving the bilateral temporal lobes. Hematological evaluation established previously unrecognized CLL. Although histopathological confirmation was not obtained, the overall clinical, radiological, and laboratory findings supported CNS involvement associated with clinically suspected RT as the most likely diagnosis. Progressive neuropsychiatric deterioration limited invasive diagnostic procedures and disease‐directed treatment. Supportive and palliative management was provided, and the patient died of aspiration pneumonia 114 days after surgery. Conclusion This case demonstrates that clinically suspected CNS RT may present predominantly with progressive psychiatric and behavioral symptoms in the absence of focal neurological deficits. Severe neuropsychiatric symptoms may themselves impede diagnostic confirmation and disease‐directed treatment. When pathological confirmation is not feasible, multidisciplinary discussion and shared decision‐making with the patient and family, together with explicit acknowledgment of diagnostic uncertainty and careful balancing of the benefits and burdens of further investigation and treatment, may support patient‐centered care.

Psychiatry and Clinical Neurosciences ReportsVol. 5(4)
Sapporo Higashi Tokushukai Hospital (JP), Sapporo Science Center (JP)
Openalex Percentile: Top 13%
Chronic Lymphocytic Leukemia Research
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