Gattuso J M, Kamm M A, Talbot J C
St Mark's Hospital, London, UK.
Gut. 1997 Aug;41(2):252-7. doi: 10.1136/gut.41.2.252.
The aetiology and pathology of both idiopathic megarectum and idiopathic megacolon are unknown. In particular, it is unknown whether there are abnormalities involving enteric nerves or smooth muscle.
Resected tissue was examined from 24 patients who underwent surgery for idiopathic megarectum, from six patients who had tissue resected for idiopathic megacolon, and 17 control patients who had surgery for non-obstructing large bowel cancer. Qualitative and quantitative histological examination was performed after staining with haematoxylin and eosin, periodic acid Schiff (PAS), Martius scarlet blue (MSB), and phosphotungstic acid haematoxylin (PTAH). Neural and glial tissue were examined after immuno-staining with S100 and PGP9.5.
Compared with controls, patients with idiopathic megarectum had significant thickening of their muscularis mucosae (median 78 v 33 microns, p < 0.005), circular muscle (1000 v 633 microns, p < 0.005), and longitudinal muscle (1083 v 303 microns, p < 0.005), despite rectal dilatation. This thickening was relatively greater in the longitudinal than in the circular muscle. Fibrosis of the longitudinal muscle was seen, using MSB staining, in 58%, of circular muscle in 38%, and of muscularis mucosae in 29% of patients. The relation between muscle thickening and fibrosis was variable. The density of neural tissue in the longitudinal muscle seemed to be reduced in patients with idiopathic megarectum. There was no thickening of enteric muscle or alteration in the density of innervation in patients with idiopathic megacolon.
There is notable thickening of the enteric smooth muscle in patients with idiopathic megarectum, but the architecture of the enteric innervation seems to be intact. Functional abnormalities of the latter remain a possible cause of the smooth muscle hypertrophy.
特发性巨直肠和特发性巨结肠的病因及病理均不明。尤其是,目前尚不清楚是否存在涉及肠神经或平滑肌的异常情况。
对24例行特发性巨直肠手术的患者、6例行特发性巨结肠组织切除的患者以及17例行非梗阻性大肠癌手术的对照患者的切除组织进行检查。用苏木精-伊红染色、过碘酸希夫(PAS)染色、马休黄猩红蓝(MSB)染色和磷钨酸苏木精(PTAH)染色后进行定性和定量组织学检查。用S100和PGP9.5免疫染色后检查神经和神经胶质组织。
与对照组相比,尽管直肠扩张,但特发性巨直肠患者的黏膜肌层(中位数78对33微米,p<0.005)、环行肌(1000对633微米,p<0.005)和纵行肌(1083对303微米,p<0.005)明显增厚。纵行肌的增厚相对大于环行肌。使用MSB染色,58%的患者纵行肌出现纤维化,38%的患者环行肌出现纤维化,29%的患者黏膜肌层出现纤维化。肌肉增厚与纤维化之间的关系各不相同。特发性巨直肠患者纵行肌中的神经组织密度似乎降低。特发性巨结肠患者的肠肌层没有增厚,神经支配密度也没有改变。
特发性巨直肠患者的肠平滑肌有明显增厚,但肠神经支配结构似乎完整。后者的功能异常仍是平滑肌肥大的可能原因。