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糜烂性息肉样增生与孤立性直肠溃疡综合征的临床病理比较

Clinicopathologic comparison of eroded polypoid hyperplasia and solitary rectal ulcer syndrome.

作者信息

Cho N H, Park C I, Ahn H J

机构信息

Department of Pathology, Yonsei University College of Medicine, Seoul, Korea.

出版信息

J Korean Med Sci. 1994 Aug;9(4):319-27. doi: 10.3346/jkms.1994.9.4.319.

Abstract

We experienced two unusual cases of tumor-like polypoid lesions involving the rectosigmoid colon. They could not be readily classified into any well known polypoid tumors of the rectosigmoid colon, but appeared to have some similarities to the previously documented "eroded polypoid hyperplasia (EPH)". A collective review of our seven cases of solitary rectal ulcer syndrome (SRUS), which proved to be due to paradoxically over-reactive muscle tone of the puborectalis, was performed, and clinicopathologic comparisons between EPH and SRUS were carried out. They shared histopathologic characteristics such as vascular congestion, crypt hyperplasia, and eroded surface, but they were different from each other in clinical symptoms, location of lesions and gross features. Furthermore, in one EPH case there was an altered much profile which was similar to that seen in SRUS and complete rectal prolapse. Conceivably, the pathological features of both EPH and SRUS were thought to have a possible connection with mucosal prolapse syndrome (MPS). Considering that MPS is a group of diseases encompassing SRUS and the related disorders of the colorectum and the anus, it is speculated that EPH of the rectosigmoid colon might be the proximal analogue of SRUS, a mucosal prolapse of the more distal colon.

摘要

我们遇到了两例不寻常的肿瘤样息肉样病变,累及直肠乙状结肠。它们难以轻易归类为直肠乙状结肠任何已知的息肉样肿瘤,但似乎与先前记录的“糜烂性息肉样增生(EPH)”有一些相似之处。我们对七例孤立性直肠溃疡综合征(SRUS)进行了汇总回顾,结果证明该综合征是由于耻骨直肠肌肌张力异常亢进所致,并对EPH和SRUS进行了临床病理比较。它们具有共同的组织病理学特征,如血管充血、隐窝增生和表面糜烂,但在临床症状、病变部位和大体特征方面彼此不同。此外,在一例EPH病例中,存在一种改变的形态,类似于SRUS和完全性直肠脱垂中所见的形态。可以想象,EPH和SRUS的病理特征被认为可能与黏膜脱垂综合征(MPS)有关。鉴于MPS是一组包括SRUS以及结直肠和肛门相关疾病的疾病,推测直肠乙状结肠的EPH可能是SRUS(更远端结肠的黏膜脱垂)的近端类似物。

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