伴多巴胺能功能障碍的迟发性口腔淋巴结病:普拉克索治疗一例疑似前驱路易体病。

IF 1.7
Hitomi Matsui, Takehiro Tamura, Masashi Kameyama, Yuki Omori, Genichi Sugihara, Takashi Takeuchi, Hidehiko Takahashi, Ko Furuta
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引用次数: 0

摘要

一名85岁的迟发性抑郁症妇女随后发展为持续性口腔淋巴结病。作为抗抑郁药的增强剂,低剂量阿立哌唑改善了情绪和口腔症状,但过度镇静和帕金森病需要逐渐减少和停药。停药后,口腔前列腺病复发,无明显抑郁恶化。多巴胺转运体单光子发射计算机断层扫描显示双侧纹状体摄取减少,123i -偏氧苄基胍心脏扫描显示摄取减少,认知功能保留。鉴于临床和影像学结果提示多巴胺能功能障碍,并在对标签外使用进行知情讨论后,开始使用每日0.25 mg的普拉克索。口腔不适在1周内减轻,2周后口服摄入量恢复正常,无不良反应;口腔症状和情绪持续缓解6个月。总体而言,该报告在概念上与前驱路易体病研究框架中描述的精神发病表型相一致,但这仍然是一种解释性考虑,而不是诊断。评估类似病例中可能涉及的多巴胺能可能有助于个体化治疗;然而,多巴胺激动剂的治疗作用需要在前瞻性研究中得到证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Late-Onset Oral Cenesthopathy With Dopaminergic Dysfunction: Therapeutic Response to Pramipexole in a Case With Suspected Prodromal Lewy Body Disease.

Late-Onset Oral Cenesthopathy With Dopaminergic Dysfunction: Therapeutic Response to Pramipexole in a Case With Suspected Prodromal Lewy Body Disease.

Late-Onset Oral Cenesthopathy With Dopaminergic Dysfunction: Therapeutic Response to Pramipexole in a Case With Suspected Prodromal Lewy Body Disease.

An 85-year-old woman with late-onset depression subsequently developed persistent oral cenesthopathy. As antidepressant augmentation, low-dose aripiprazole improved both mood and oral symptoms, but oversedation and parkinsonism necessitated tapering and discontinuation. After discontinuation, oral cenesthopathy recurred without clear depressive worsening. Dopamine transporter single-photon emission computed tomography showed reduced bilateral striatal uptake and 123I-metaiodobenzylguanidine cardiac scintigraphy showed decreased uptake, with preserved cognition. In light of the clinical and imaging findings suggestive of dopaminergic dysfunction, and after an informed discussion of off-label use, pramipexole 0.25 mg daily was initiated. Oral discomfort lessened within 1 week and oral intake normalised by 2 weeks, without adverse effects; remission of oral symptoms and mood persisted for 6 months. Overall, the presentation was conceptually compatible with the psychiatric-onset phenotype described in the prodromal Lewy body disease research framework, but this remains an interpretive consideration rather than a diagnosis. Assessing possible dopaminergic involvement in similar cases of oral cenesthopathy may aid individualised management; however, the therapeutic role of dopamine agonists requires confirmation in prospective studies.

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