Peripheral nervous system alterations in small cell lung cancer. Clinico-pathological study.

Neuropatologia polska Pub Date : 1992-01-01
E Kida, M Barcikowska, T Michalska, E Joachimowicz, A Siekierzyńska
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Abstract

Small cell lung cancer (SCLC) is one of the most malignant tumors, especially often associated with nonmetastatic neurological disorders, corresponding to paraneoplastic neurological syndromes. The pathogenesis of which is unknown, however, mostly attributed to autoimmune processes. The aim of the study was to determine the pattern of the peripheral nervous system damage in SCLC. To provide further data contributing to the pathomechanism underlying these syndromes, immunocytochemical studies were initiated. Autopsy material was collected from 47 cases of SCLC. All these patients were examined clinically. The sections from the cervical, thoracic and lumbosacral segments of the spinal cord with spinal roots and dorsal root ganglia were taken. For immunohistochemistry following antisera were used: GFAP, MBP, IgG, IgM, ferritin, ubiquitin, alpha 1-antichymotrypsin, alpha 2-macroglobulin, C3 and C5b9 complement fractions. In 18 patients peripheral nervous system disturbances were diagnosed neurologically, 21 of cases presented neuromuscular disorders by emg. Among the nonmetastatic lesions most often a damage of dorsal root ganglia was observed (in 33 cases). Degeneration of the spinal roots was absent only in 8 cases. In 21 cases degenerative changes of motor neurons within anterior horn were present. In no case ubiquitin-positive inclusion bodies within the motor neurons could be found. In 8 cases extravasation of the IgG with diffuse labeling of the grey matter was observed. IgM immunoreactivity was markedly less frequently present, C5b9 complement fraction immunoreactivity was also confined only to cases with peripheral nervous system disturbances. Therefore, our preliminary data seem to confirm the participation of humoral immunity in paraneoplastic syndrome pathogenesis.

小细胞肺癌的周围神经系统改变。二研究。
小细胞肺癌(SCLC)是最恶性的肿瘤之一,尤其常伴有非转移性神经系统疾病,对应于副肿瘤神经系统综合征。然而,其发病机制尚不清楚,主要归因于自身免疫过程。该研究的目的是确定SCLC周围神经系统损伤的模式。为了进一步了解这些综合征的病理机制,免疫细胞化学研究开始了。收集了47例SCLC的尸检资料。所有患者均进行临床检查。取脊髓颈、胸、腰骶段与脊髓根、背根神经节段切片。免疫组化采用抗血清:GFAP、MBP、IgG、IgM、铁蛋白、泛素、α 1-抗凝乳胰蛋白酶、α 2-巨球蛋白、C3和C5b9补体部分。18例患者经神经学诊断为周围神经系统障碍,21例经肌电图诊断为神经肌肉障碍。在非转移性病变中,最常观察到背根神经节的损害(33例)。仅8例未见脊髓根退变。21例前角运动神经元出现退行性改变。在任何情况下,运动神经元内都找不到泛素阳性包涵体。8例观察到IgG外渗伴灰质弥漫性标记。IgM免疫反应性明显较少,C5b9补体部分免疫反应性也仅局限于周围神经系统紊乱的病例。因此,我们的初步数据似乎证实了体液免疫参与副肿瘤综合征的发病机制。
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