Sato T, Ito H, Miyazaki S, Komine S, Hayashida Y
Department of Pediatrics, Saga Medical School, Japan.
Acta Paediatr Jpn. 1993 Aug;35(4):358-60. doi: 10.1111/j.1442-200x.1993.tb03071.x.
We report a 14 month old male infant with Ehlers-Danlos syndrome who became 'anuric' due to an acutely dilated urinary bladder. Although the patient was also found to have megacolon, no diverticulum was seen in his gastrointestinal tract or urinary bladder. In order to decompress the urinary bladder and colonic wall, we put an indwelling urinary catheter in place for 2 months, and carried out daily glycerin enema for 3 months. All urological and gastrointestinal symptoms subsided with this intensive medical treatment. The diagnosis of megacystis and megacolon was made very early in life for this patient. This may indicate that the striking extension of gastrointestinal and bladder wall may lead to the development of diverticula of gastrointestinal and urinary tracts in later life.
我们报告一名患有埃勒斯-当洛综合征的14个月大男婴,其因急性扩张的膀胱而出现“无尿”。尽管该患者还被发现患有巨结肠,但在其胃肠道或膀胱中未发现憩室。为了使膀胱和结肠壁减压,我们留置导尿管2个月,并进行了3个月的每日甘油灌肠。经过这种强化治疗,所有泌尿系统和胃肠道症状均消退。该患者在生命早期就被诊断出患有巨膀胱和巨结肠。这可能表明胃肠道和膀胱壁的显著扩张可能会导致日后胃肠道和泌尿道憩室的形成。