1. Anti-Cholinergic Derangement of Cortical Metabolism on 18F-FDG PET in a Patient with Frontotemporal Lobar Degeneration Dementia: A Case of the TREDEM Registry
- Author
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Daniela Perra, Laura Bonanni, Maurizio Gallucci, Maria Elena Di Battista, Daniela Galimberti, Chiara Fenoglio, Claudia Pallucca, Cristina Bergamelli, Maria Serpente, Franco Boccaletto, Gianluigi Zanusso, Michele Fiorini, and Vittorio Fiore
- Subjects
Male ,0301 basic medicine ,Neuroimaging ,Muscarinic Antagonists ,Biperiden ,03 medical and health sciences ,0302 clinical medicine ,Fluorodeoxyglucose F18 ,medicine ,Humans ,Dementia ,Anti-cholinergics ,PET scan ,TREDEM ,cerebral cortex ,frontotemporal dementia ,Aged ,Cerebral Cortex ,Temporal cortex ,business.industry ,Dementia with Lewy bodies ,General Neuroscience ,Neuropsychology ,General Medicine ,Frontotemporal lobar degeneration ,Mental Status and Dementia Tests ,medicine.disease ,Psychiatry and Mental health ,Clinical Psychology ,030104 developmental biology ,Frontal lobe ,Frontotemporal Dementia ,Positron-Emission Tomography ,Anesthesia ,Geriatrics and Gerontology ,business ,030217 neurology & neurosurgery ,medicine.drug ,Frontotemporal dementia - Abstract
We present the case of a patient with an atypical course of frontotemporal lobar degeneration (FTLD) complicated by the use of an anticholinergic drug. A 70-year-old patient, followed by psychiatrists for depression and behavioral disorders, received a diagnosis of dementia with Lewy bodies (DLB) at another Center due to auditory hallucinations, gait impairment, and tendency to fall. He was then admitted to our Memory Clinic Unit for behavioral disturbances, such as delusional thinking, auditory hallucinations, and memory complaints. At that time, the patient's therapy included Lorazepam, Quetiapine, Promazine, and Biperiden. The latter was immediately suspended for the absence of extrapyramidal signs and to avoid the anticholinergic cognitive side effects. A 18F-FDG PET showed a derangement of cortical metabolism with diffusely reduced activity, and limited areas of hyperactivity involving lateral frontal and lateral temporal inferior regions bilaterally. The patient underwent a series of exams, including neuropsychological tests, 123I-MIBG scintigraphy, cerebrospinal fluid examination, and genetic analysis. A second 18F-FDG PET showed an extensive remodulation of metabolic activity: relative higher concentration of the tracer in the prefrontal and inferior temporal cortex was no more detectable. Similarly, the diffuse reduced metabolic activity could not be traced anymore. Nonetheless, the metabolic activity still appeared reduced in the frontal lobe, in the anterior cingulate bilaterally, and in the anterior part of the hemispheric fissure. Taken together, clinical and neuroimaging features would point to a FTLD-like form. Furthermore, the diagnostic work-up was likely confounded by the anticholinergic drug on 18F-FDG PET, highlighting the importance of carefully checking the patient's pharmacology during the diagnostic process.
- Published
- 2020