Calì A, Berni Canani M, De Luca L, Terracciano L, Berni Canani R, Chiummariello S
Istituto di Anatomia Patologia, IIa Facoltà di Medicina e Chirurgia, Napoli, Italia.
Pediatr Med Chir. 1991 Jul-Aug;13(4):351-4.
For the frequent remark in childhood of relapsing bronchitis and/or broncho-pneumonic sickness we resolved to use for the differential diagnosis the nasal brushing method according to Rutland (for samples of ciliated epithelium from the deep surface of the inferior nasal turbinate using a 2 mm diameter nasal brush. The samples were used for ultrastructural study of cilia.
Children studied 22:14 (6-14) y.old with relapsing bronchitis, 4 with relapsing broncho-pneumonitis, 1 Nemaline myopathy (n.m.) with heavy respiratory insufficiency; 3 Werdnig Hoffmann syndromes (W.H.). Control group of 4 normal children. In the control group and 14 relapsing bronchitis normal tubular pattern (9 + 2) and ciliary conformation were present; in the relapsing broncho-pneumonic syndrome group, 2 children presented deficiency of some brace dynein arms = chronic inflammation; in the Nemaline myopathy we noted total lack of interior dynein arms with random cilia orientation; in the 3 W.H. = normal cilia conformation. The authors noted for the heavy respiratory insufficiency of the Nemaline myopathy the presence of immotile cilia and discuss possibility that in all Nemaline myopathy syndromes this association may be present (a new syndrome?). The W.H. myopathy is characterized by normal cilia aspects and the respiratory insufficiency is caused by muscular respiratory insufficiency secondary to anterior spinal corn horn. In the Nemaline myopathy the same genetic defect can act in muscular fibres and on dynain arms (cytoskeleton). The technique described is suitable for processing epithelial brushings from other parts of the respiratory tract.(ABSTRACT TRUNCATED AT 250 WORDS)
针对儿童期频繁复发的支气管炎和/或支气管肺炎,我们决定采用鲁特兰的鼻刷法进行鉴别诊断(使用直径2毫米的鼻刷从下鼻甲深部表面获取纤毛上皮样本,样本用于纤毛的超微结构研究)。
研究对象为22名年龄在6至14岁的复发性支气管炎患儿、4名复发性支气管肺炎患儿、1名患有严重呼吸功能不全的线状体肌病患儿以及3名韦尔尼克-霍夫曼综合征患儿。对照组为4名正常儿童。对照组和14名复发性支气管炎患儿的纤毛呈现正常的管状模式(9 + 2)和形态;在复发性支气管肺炎综合征组中,2名患儿存在部分支撑动力蛋白臂缺失,即慢性炎症;在线状体肌病患儿中,我们发现内部动力蛋白臂完全缺失且纤毛随机排列;在3名韦尔尼克-霍夫曼综合征患儿中,纤毛形态正常。作者指出,线状体肌病患儿严重呼吸功能不全伴有纤毛运动障碍,并探讨了所有线状体肌病综合征中可能存在这种关联(一种新综合征?)的可能性。韦尔尼克-霍夫曼肌病的特征是纤毛外观正常,呼吸功能不全是由脊髓前角继发的肌肉呼吸功能不全引起的。在线状体肌病中,相同的基因缺陷可作用于肌纤维和动力蛋白臂(细胞骨架)。所描述的技术适用于处理呼吸道其他部位的上皮刷检样本。(摘要截断于250字)