Basilisco G, Velio P, Bianchi P A
Cattedra di Gastroenterologia, Università degli Studi di Milano, IRCCS-Ospedale Maggiore di Milano, Italy.
Gut. 1997 Feb;40(2):188-91. doi: 10.1136/gut.40.2.188.
Oesophageal motility is often impaired in patients with megaduodenum and other forms of intestinal pseudo-obstruction in which a visceral myopathy or neuropathy may be present. Idiopathic longstanding megacolon with onset in adult life is still a poorly defined entity, which may also be part of a more widespread motility disorder but in which oesophageal motility has not been yet systematically studied.
To assess oesophageal motility in patients with longstanding idiopathic megacolon with onset in adult life.
14 consecutive subjects with idiopathic megacolon whose symptoms began after the age of 10 and a clinical history of 2-22 years.
Standard barium enema, water perfused oesophageal manometry, and also anorectal manometry.
Oesophageal motility was impaired in five patients (36%; 95% confidence intervals 16 to 61%). Normal peristalsis was substituted by low amplitude multiple peaked simultaneous contractions in four subjects and by undetectable contractions in one. In three of them the lower oesophageal sphincter did not relax after swallows; in the same patients anal relaxation after rectal distension was also undetectable. All five patients with impaired oesophageal motility had a colonic dilatation sparing the rectum. Three of them reported constipation and a history of pesudo-obstruction and the other two only abdominal distension.
Oesophageal manometry should be performed in patients with longstanding idiopathic megacolon with onset in adult life, in particular if the rectum is not dilated and even in absence of pseudo-obstruction. This simple test may disclose a more widespread visceral neuropathy or myopathy. Such a diagnosis helps to better understand the cause of the colonic dilatation and may be clinically relevant for treatment of the patients.
巨十二指肠患者以及其他形式的肠道假性梗阻患者常存在食管动力障碍,这些患者可能存在内脏肌病或神经病变。成人期发病的特发性长期巨结肠仍是一个定义不清的实体,它也可能是更广泛的动力障碍的一部分,但食管动力尚未得到系统研究。
评估成人期发病的长期特发性巨结肠患者的食管动力。
14例连续的特发性巨结肠患者,其症状始于10岁以后,临床病史为2至22年。
标准钡灌肠、水灌注食管测压以及肛门直肠测压。
5例患者(36%;95%置信区间为16%至61%)存在食管动力障碍。4例患者正常蠕动被低振幅多峰同步收缩所替代,1例患者未检测到收缩。其中3例患者吞咽后食管下括约肌不松弛;同样这3例患者直肠扩张后肛门也无松弛。所有5例食管动力障碍患者的结肠扩张均不累及直肠。其中3例患者有便秘及假性梗阻病史,另外2例仅有腹胀。
对于成人期发病的长期特发性巨结肠患者,尤其是直肠未扩张甚至无假性梗阻的患者,应进行食管测压。这项简单的检查可能揭示更广泛的内脏神经病变或肌病。这样的诊断有助于更好地理解结肠扩张的原因,并且可能对患者的治疗具有临床意义。