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病例报告:F-FDG PET/CT在单克隆丙种球蛋白病相关性周围神经病中识别浆细胞瘤的应用

Case Report: Application of F-FDG PET/CT in identifying plasmacytoma in monoclonal gammopathy associated peripheral neuropathy.

作者信息

Weng Jiequn, Lin Jie, Sun Chong

机构信息

Department of Neurology, Yuyao People's Hospital of Zhejiang Province, Yuyao, Zhejiang, China.

Department of Neurology, Huashan Hospital, Fudan University, Shanghai, China.

出版信息

Front Nucl Med. 2024 Aug 14;4:1446780. doi: 10.3389/fnume.2024.1446780. eCollection 2024.

Abstract

Peripheral neuropathy is a prevalent complication in plasma cell disorders, posing significant diagnostic and therapeutic challenges. This study presents three cases initially diagnosed with chronic inflammatory demyelinating polyneuropathy (CIDP). Despite initial symptom regression post-immunomodulatory treatment, the patients exhibited progressive neurological deficits. Advanced laboratory evaluation confirmed monoclonal protein presence, yet traditional diagnostic methods, including bone marrow biopsy and flow cytometry, yielded normal results. Utilizing F-FDG PET/CT, we identified multiple hypermetabolic vertebral lesions, which upon biopsy, confirmed the diagnosis of plasmacytoma. Our findings underscore the utility of PET/CT as a reliable diagnostic tool for monoclonal gammopathy associated neuropathy, advocating for its consideration in cases with equivocal diagnosis. When the diagnosis is in doubt, biopsy of a lesion may facilitate early and accurate diagnosis, potentially influencing treatment strategies and patient outcomes.

摘要

周围神经病变是浆细胞疾病中常见的并发症,带来了重大的诊断和治疗挑战。本研究报告了3例最初被诊断为慢性炎症性脱髓鞘性多发性神经病(CIDP)的病例。尽管免疫调节治疗后初始症状有所缓解,但患者仍出现进行性神经功能缺损。进一步的实验室评估证实存在单克隆蛋白,但包括骨髓活检和流式细胞术在内的传统诊断方法结果均正常。利用F-FDG PET/CT,我们发现了多个代谢增高的椎体病变,经活检确诊为浆细胞瘤。我们的研究结果强调了PET/CT作为单克隆丙种球蛋白病相关性神经病可靠诊断工具的实用性,主张在诊断不明确的病例中考虑使用。当诊断存疑时,对病变进行活检可能有助于早期准确诊断, potentially influencing treatment strategies and patient outcomes.(原文此处有误,正确的翻译应该是“可能会影响治疗策略和患者预后”) 从而可能影响治疗策略和患者预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1ce/11440967/4a2191d8964f/fnume-04-1446780-g001.jpg

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