Cucchiara S, Annese V, Minella R, Franco M T, Iervolino C, Emiliano M, Auricchio S
Department of Paediatrics, Second School of Medicine, University of Naples, Italy.
J Pediatr Gastroenterol Nutr. 1994 Apr;18(3):294-305. doi: 10.1097/00005176-199404000-00008.
We analyzed the antroduodenojejunal (ADJ) manometric patterns in a group of 19 consecutive children (mean age, 53 months; range, 5 months to 14 years) referred for suspected chronic idiopathic intestinal pseudoobstruction. Diagnosis was based on typical symptoms, absence of extraintestinal diseases, and structural lesions of the gut at endoscopy and radiology. Surgical full-thickness intestinal biopsies were evaluated in nine patients. Manometry of the stomach and small bowel was performed in the fasting and fed state with a multilumen perfused probe. All patients showed severe abnormalities of ADJ motor activity that were not seen in the eight controls (mean age, 38.2 months; range, 1-9 years). In 12 patients, manometric patterns suggesting neuropathic disease were detected with fasting and/or fed sustained and incoordinated duodenojejunal phasic waves, aberrant propagation and/or configuration of phase III of the inter-digestive motility complex, inability of a meal to convert a fasting into a fed pattern, and prolonged groups of fasting and fed nonpropagated phasic waves. In seven of these patients, histology revealed marked changes of the intrinsic neurons. In four cases, manometry disclosed features suggestive of a myogenic disease, including severe fasting and fed infrequent low-amplitude contractions, sometimes with some degree of propagation; in two of these cases, histology showed morphological abnormalities of smooth muscle cells of the gut wall. In three patients, manometry revealed signs suggestive of mechanical obstruction of the gut, such as repetitive post-feeding clusters and simultaneous repeated broad-based waves; in these patients, more detailed x-ray studies showed organic obstructive causes (ileal lymphoma, Hirschsprung's disease, and intestinal malrotation).(ABSTRACT TRUNCATED AT 250 WORDS)
我们分析了一组连续19例疑似慢性特发性肠道假性梗阻儿童(平均年龄53个月;范围5个月至14岁)的胃十二指肠空肠(ADJ)测压模式。诊断基于典型症状、无肠道外疾病以及内镜和放射学检查时肠道无结构病变。对9例患者进行了手术全层肠活检。使用多腔灌注探头在禁食和进食状态下对胃和小肠进行测压。所有患者均显示ADJ运动活动严重异常,而8名对照组患者(平均年龄38.2个月;范围1 - 9岁)未出现这种情况。12例患者中,通过禁食和/或进食时持续且不协调的十二指肠空肠相波、消化间期运动复合波III期的异常传播和/或形态、进食未能将禁食模式转变为进食模式以及禁食和进食时延长的非传播性相波群,检测到提示神经病变的测压模式。其中7例患者的组织学检查显示内在神经元有明显变化。4例患者的测压结果显示提示肌源性疾病的特征,包括严重的禁食和进食时低频低幅收缩,有时伴有一定程度的传播;其中2例患者的组织学检查显示肠壁平滑肌细胞形态异常。3例患者的测压结果显示提示肠道机械性梗阻的迹象,如进食后重复性簇状波和同时出现的重复宽基波;在这些患者中,更详细的X线检查显示存在器质性梗阻原因(回肠淋巴瘤、先天性巨结肠和肠旋转不良)。(摘要截断于250字)