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慢性原发性肠道假性梗阻

Chronic primary intestinal pseudo-obstruction.

作者信息

Hanks J B, Meyers W C, Andersen D K, Woodard B H, Peete W P, Garbutt J T, Jones R S

出版信息

Surgery. 1981 Feb;89(2):175-82.

PMID:6893876
Abstract

Chronic primary intestinal pseudo-obstruction (CPIP) has received attention despite of its unclear etiology and infrequent occurrence. Recently a patient with this disorder had evidence of a primary visceral neuropathy. Reviewing the literature, we found 30 case reports of CPIP and evaluated their clinicopathologic findings. Presenting symptoms and radiologic findings were nonspecific. Esophageal motility was abnormal in 12 of 14 reports. Intestinal histopathology revealed normal muscle wall, mucosa, and ganglion cells in over 50% of reports. Only 48% of cases demonstrated clinical improvement. Thirty percent (8 of 30) ultimately died. We conclude that CPIP is a perplexing, often fatal entity that can mimic mechanical obstruction in the absence of definite etiology. Primary neurologic or muscular disease may be a possible explanation, but, as yet, definite documentation does not exist.

摘要

尽管慢性原发性肠假性梗阻(CPIP)病因不明且发病率较低,但仍受到了关注。最近,一名患有这种疾病的患者有原发性内脏神经病变的证据。通过回顾文献,我们发现了30例CPIP病例报告,并评估了它们的临床病理特征。呈现出的症状和放射学表现并无特异性。在14份报告中有12份显示食管动力异常。超过50%的报告中肠道组织病理学显示肌壁、黏膜和神经节细胞正常。只有48%的病例显示临床症状有所改善。30%(30例中的8例)最终死亡。我们得出结论,CPIP是一种令人困惑的、通常致命的疾病,在没有明确病因的情况下可模拟机械性梗阻。原发性神经或肌肉疾病可能是一种解释,但目前尚无确切证据。

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