Laboratory of Neuropathology, Department of Neurology, Peking University First Hospital, Beijing 100034, China.
Pediatr Neurol. 2010 Aug;43(2):103-9. doi: 10.1016/j.pediatrneurol.2010.04.001.
Nonuniform pathologic changes in chronic inflammatory demyelinating polyneuropathy were previously reported only in adult humans. We analyzed the pathologic features of 12 children, aged 2-17 years, with chronic inflammatory demyelinating polyneuropathy. Six patients manifested a preceding illness. Five patients presented a chronic, monophasic course, and seven presented a relapsing-remitting course. Three patients exhibited multiple cranial-nerve involvement. Five of 12 (41.7%) patients presented nonuniform features. Two subtypes of nonuniform lesions were revealed. One exhibited varying myelinated fiber content between nerve fascicles, and one exhibited onion bulbs involving a variable number of fascicles. Macrophages were evident in 11 patients, and the number of CD3-positive T cells in the nonuniform group was greater compared with the uniform group (P = 0.045). Our results demonstrate that childhood chronic inflammatory demyelinating polyneuropathy exhibits pathologically nonuniform features, thus providing more evidence to assist in differential diagnoses of pediatric patients. However, clinical and electrophysiologic features, as well as responses to treatment, were similar in the nonuniform and uniform groups.
先前仅在成人慢性炎症性脱髓鞘性多发性神经病中报道过非均质性病理改变。我们分析了 12 名年龄在 2-17 岁的慢性炎症性脱髓鞘性多发性神经病患儿的病理特征。6 名患者有前驱疾病。5 名患者表现为慢性单相病程,7 名患者表现为复发缓解病程。3 名患者表现为多颅神经受累。12 例中有 5 例(41.7%)表现为非均质性特征。显示出两种类型的非均质性病变。一种表现为神经束之间有不同的有髓纤维含量,另一种表现为洋葱球样结构,涉及数量不等的束。11 例中均有巨噬细胞浸润,非均质性组的 CD3 阳性 T 细胞数量多于均质性组(P=0.045)。我们的结果表明,儿童慢性炎症性脱髓鞘性多发性神经病在病理上表现出非均质性特征,从而为协助儿科患者的鉴别诊断提供了更多证据。然而,非均质性组和均质性组的临床和电生理特征以及对治疗的反应相似。