Kovács Tibor, Papp Mátyás I, Cairns Nigel J, Khan M Nadeem, Lantos Peter L
Department of Neurology, Semmelweis University, Faculty of General Medicine, Budapest, Hungary.
Mov Disord. 2003 Aug;18(8):938-42. doi: 10.1002/mds.10466.
Olfactory dysfunction is a characteristic clinical sign in Parkinson's disease (PD); it is also present in multiple system atrophy (MSA). The pathological basis of hyposmia or anosmia in PD is well known: the olfactory bulb (OB) contains numerous Lewy bodies and severe neuronal loss is present in the anterior olfactory nucleus (AON). We established that glial cytoplasmic inclusions (GCIs) are present in all the OBs from MSA cases. Their presence in the OB is diagnostic for MSA. Additionally, neuronal loss is present in the AON in MSA. These pathological changes might be responsible for the olfactory dysfunction seen in MSA.
嗅觉功能障碍是帕金森病(PD)的一个典型临床体征;在多系统萎缩(MSA)中也存在。PD 患者嗅觉减退或嗅觉丧失的病理基础已为人所知:嗅球(OB)含有大量路易小体,前嗅核(AON)存在严重的神经元丢失。我们发现多系统萎缩(MSA)病例的所有嗅球中均存在胶质细胞胞质内包涵体(GCI)。它们在嗅球中的存在是多系统萎缩(MSA)的诊断依据。此外,多系统萎缩(MSA)的前嗅核中也存在神经元丢失。这些病理变化可能是多系统萎缩(MSA)中嗅觉功能障碍的原因。