Department of Neurology, Marmara University Hospital, Tophanelioğlu cad. 13/15, Altunizade, Istanbul, Turkey.
Neurol Sci. 2010 Dec;31(6):813-6. doi: 10.1007/s10072-010-0288-3. Epub 2010 May 8.
Pandysautonomia is a severe and rare clinical condition characterized by widespread sympathetic and parasympathetic dysfunction. Consideration of whether symptoms and presentation are acute, subacute, or chronic is often helpful in establishing a differential diagnosis. The underlying mechanisms leading to pure pandysautonomia are unclear; however, there is some evidence suggestive of an immune-mediated pathogenesis. Herein, we report a case with pandysautonomia as a paraneoplastic manifestation of non-small cell lung cancer that had an excellent response to symptomatic and supportive treatments, as well as IVIG therapy.
全自主神经功能衰竭是一种严重且罕见的临床病症,其特征为广泛的交感神经和副交感神经功能障碍。考虑症状和表现是急性、亚急性还是慢性,往往有助于建立鉴别诊断。导致单纯全自主神经功能衰竭的潜在机制尚不清楚;然而,有一些证据表明其发病机制与免疫有关。在此,我们报告了一例全自主神经功能衰竭病例,其为非小细胞肺癌的副瘤表现,对症状和支持治疗以及静脉注射免疫球蛋白治疗有极好的反应。