18F-FDG PET/CT as a molecular biomarker in the diagnosis of amyotrophic lateral sclerosis associated with prostate cancer and progressive supranuclear palsy: A case report.

Emilly A Cortés Mancera, Fabio A Sinisterra Solis, Francisco R Romero-Castellanos, Ivan E Diaz-Meneses, Nora E Kerik-Rotenberg
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Abstract

Introduction: Amyotrophic lateral sclerosis (ALS) is a neurodegenerative, multisystem disorder. Its clinical presentation typically consists of progressive focal muscle atrophy and weakness. In addition to motor disorders, the association between ALS and cancer has been researched, such as frontotemporal dementia and progressive supranuclear palsy. The diagnosis is based primarily on the clinical history, physical examination, electrodiagnostic tests (with an EMG needle), and neuroimaging, such as MRI and 18F-FDG PET/CT.

Presentation of the case: A 67-year-old male patient was diagnosed with prostate adenocarcinoma with a clinical picture of muscle weakness in the lower limbs that caused falls and was associated with fasciculations in the thighs and arms, alterations in the tone of voice, poor memory, and difficulty articulating words. In the neurological assessment, he described walking supported by a walker with decreased strength in both lower limbs and sensitivity without alterations. The diagnoses of upper and lower motor neuron disease and probable ALS were integrated. Furthermore, the probable coexistence of frontotemporal dementia/disorder (FDD) with ALS was considered. The main findings in the 18F-FDG PET/CT study was hypometabolism in the cortex of the bilateral motor and premotor areas, the anterior cingulate, both caudate and putamen, a metabolic pattern compatible with ALS, and progressive supranuclear palsy.

Conclusion: Through the PET/CT studies, we demonstrated a case in which ALS, prostate cancer and progressive supranuclear palsy coexisted molecularly; it was clinically difficult to diagnose. Molecular imaging has potential in the diagnostic and prognostic evaluation of ALS. It is crucial to identify the disease early and reliably through metabolic patterns that allow us to confirm the disease or differentiate it from other pathologies.

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18F-FDG PET/CT作为分子生物标志物诊断肌萎缩性脊髓侧索硬化症伴前列腺癌症和进行性核上性麻痹的病例报告
肌萎缩侧索硬化症(ALS)是一种神经退行性多系统疾病。其临床表现通常包括进行性局灶性肌肉萎缩和无力。除了运动障碍外,还研究了ALS与癌症之间的关系,如额颞叶痴呆和进行性核上性麻痹。诊断主要基于临床病史、体格检查、电诊断测试(使用EMG针)和神经成像,如MRI和18F-FDG PET/CT。病例介绍一名67岁的男性患者被诊断为前列腺癌,临床表现为下肢肌肉无力,导致跌倒,并与大腿和手臂的神经束、语调改变、记忆力差和发音困难有关。在神经系统评估中,他描述了由助行器支撑的行走,双下肢力量下降,灵敏度没有改变。对上下运动神经元疾病和可能的ALS的诊断进行了整合。此外,还考虑了额颞叶痴呆/障碍(FDD)与ALS的可能共存。18F-FDG PET/CT研究的主要发现是双侧运动和前运动区皮质、前扣带、尾状核和壳核的代谢低下,这是一种与ALS兼容的代谢模式,以及进行性核上性麻痹。结论通过PET/CT研究,我们证实了一例ALS、前列腺癌症和进行性核上性麻痹分子共存的病例;临床上很难诊断。分子成像在ALS的诊断和预后评估中具有潜力。至关重要的是,通过代谢模式早期可靠地识别疾病,使我们能够确认疾病或将其与其他病理区分开来。
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