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特发性少经:一种临床病理实体——发病机制与治疗

Idiopathic oligofecorrhea: a clinicopathologic entity--pathogenesis and treatment.

作者信息

Shafik A

机构信息

Department of Surgery, Faculty of Medicine, Cairo University, Egypt.

出版信息

Digestion. 1991;48(1):51-8. doi: 10.1159/000200663.

Abstract

Oligofecorrhea is the term applied for infrequent defecation (2 or less stools per week). 146 patients with oligofecorrhea were studied. Investigations comprised radiologic, endoscopic, intestinal transit and rectal pressure studies. EMG for levator and sphincteric muscles as well as internal sphincter biopsy were done. The 146 patients could be categorized into 3 stages according to clinical and investigative results. However, the 3 stages share major abnormal findings which comprise high resting rectal neck pressure, reduced or absent recto-inhibitory reflex, internal sphincter hypertrophy and degeneration of the nerve plexus of the internal sphincter. A new theory of pathogenesis of oligofecorrhea is put forward. It is believed that innervation abnormalities of the internal sphincter interferes with the recto-inhibitory reflex action with a resulting failure of the internal sphincter to relax upon rectal distension. It seems that the degenerative changes of the nerve plexus affect mainly the parasympathetic supply leading to sympathetic overactivity. The latter leads to abnormal internal sphincter contraction which eventually results in muscle hypertrophy. Internal sphincter myotomy showed a mean improvement of 90.4% in all the cases. The stool frequency and rectal neck pressure were normalized.

摘要

少粪便是用于描述排便不频繁(每周排便2次或更少)的术语。对146例少粪便患者进行了研究。检查包括放射学、内镜检查、肠道转运和直肠压力研究。对提肌和括约肌进行了肌电图检查,并进行了内括约肌活检。根据临床和检查结果,146例患者可分为3个阶段。然而,这3个阶段有共同的主要异常表现,包括直肠颈部静息压力高、直肠抑制反射减弱或消失、内括约肌肥大以及内括约肌神经丛变性。提出了少粪便发病机制的新理论。据信,内括约肌的神经支配异常会干扰直肠抑制反射作用,导致直肠扩张时内括约肌无法松弛。神经丛的退行性改变似乎主要影响副交感神经供应,导致交感神经活动过度。后者导致内括约肌异常收缩,最终导致肌肉肥大。内括约肌切开术在所有病例中平均改善率为90.4%。排便频率和直肠颈部压力恢复正常。

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