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三例原发性梗阻性巨输尿管合并输尿管异位开口患者的膀胱输尿管连接部

The vesico-ureteric junction in three cases of primary obstructive megaureter associated with ectopic ureteric insertion.

作者信息

Dixon J S, Jen P Y, Yeung C K, Gosling J A

机构信息

Department of Anatomy, Chinese University of Hong Kong, Shatin, New Territories.

出版信息

Br J Urol. 1998 Apr;81(4):580-4. doi: 10.1046/j.1464-410x.1998.00610.x.

Abstract

OBJECTIVE

To examine the histological structure and autonomic innervation of the vesico-ureteric junction (VUJ) in three cases of primary obstructive megaureter occurring in association with ectopic ureteric insertion.

PATIENTS AND METHODS

Specimens of VUJ were obtained from one male and two females with primary obstructive megaureter and ectopic ureteric insertions. Serial frozen sections were cut and stained with either Masson's trichrome or immunostained for protein gene product (PGP 9.5; a general nerve marker) or dopamine beta-hydroxylase (DbetaH), a marker for noradrenergic nerves.

RESULTS

In each case examined the terminal ureter was encircled by a thick collar of smooth muscle on the inside of which lay normal narrow-diameter longitudinally orientated ureteric muscle bundles. Loose connective tissue separated the surrounding detrusor muscle from this abnormal muscle collar, which was formed of distinctive smooth muscle cells arranged in a meshwork. The autonomic innervation of the ureteric and detrusor muscle bundles was similar to that previously reported for the normal VUJ while the thick muscle collar was richly innervated by DbetaH-immunoreactive noradrenergic nerves.

CONCLUSION

The presence of an additional smooth muscle collar surrounding the terminal ureter may impede the normal flow of urine from ureter to bladder and be the cause of megaureter in these patients. We propose that the presence of this muscular collar arises from the developmental anomaly and suggest that these cases represent a subgroup that requires early surgical treatment.

摘要

目的

研究3例原发性梗阻性巨输尿管合并输尿管异位开口患者的膀胱输尿管连接部(VUJ)的组织结构和自主神经支配情况。

患者与方法

VUJ标本取自1例男性和2例女性原发性梗阻性巨输尿管合并输尿管异位开口患者。制作连续冰冻切片,分别进行Masson三色染色、蛋白质基因产物(PGP 9.5;一种通用神经标志物)免疫染色或多巴胺β-羟化酶(DbetaH,去甲肾上腺素能神经标志物)免疫染色。

结果

在每例患者中,输尿管末端被一层厚厚的平滑肌环包围,其内侧为正常的窄径纵向排列的输尿管肌束。疏松结缔组织将周围的逼尿肌与这个异常的肌环分隔开,该肌环由排列成网状的独特平滑肌细胞构成。输尿管和逼尿肌束的自主神经支配与先前报道的正常VUJ相似,而厚厚的肌环富含DbetaH免疫反应性去甲肾上腺素能神经。

结论

输尿管末端周围额外平滑肌环的存在可能会阻碍尿液从输尿管正常流入膀胱,是这些患者巨输尿管的病因。我们认为这种肌环的存在源于发育异常,并提示这些病例代表了一个需要早期手术治疗的亚组。

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