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家族性淀粉样变性伴多发性神经病:胃肠道受累的X线及胃镜表现

Familial amyloidosis with polyneuropathy: roentgenological and gastroscopic appearance of gastrointestinal involvement.

作者信息

Steen L E, Oberg L

出版信息

Am J Gastroenterol. 1983 Jul;78(7):417-20.

PMID:6307041
Abstract

Forty-three patients suffering from familial amyloidosis with polyneuropathy were examined by means of barium meal, barium follow through, barium enema, cholecystogram, and gastroscopy. The findings were reviewed with respect to the presence of steatorrhea and impaired d-xylose absorption. Seven patients had gastric stasis (without gross anatomical changes) on barium meal examination and seven others on the gastroscopy. Gastroscopy revealed that another five patients had inactive peristalsis of the antrum-pylorus. Only one patient had slow transit of barium on follow through. The transit time of barium did not correlate with increased fecal fat output or decreased d-xylose absorption. Barium enema and cholecystogram were normal. The main radiological and gastroscopic finding in familial amyloidosis with polyneuropathy was reduced gastric motility.

摘要

对43例患有家族性淀粉样变性伴多发性神经病的患者进行了钡餐、钡剂通过检查、钡灌肠、胆囊造影和胃镜检查。根据脂肪泻和d-木糖吸收受损的情况对检查结果进行了复查。钡餐检查发现7例患者有胃潴留(无明显解剖学改变),胃镜检查又发现7例。胃镜检查显示另有5例患者胃窦-幽门蠕动减弱。钡剂通过检查仅1例患者钡剂通过缓慢。钡剂通过时间与粪便脂肪排出量增加或d-木糖吸收减少无关。钡灌肠和胆囊造影均正常。家族性淀粉样变性伴多发性神经病的主要放射学和胃镜检查结果是胃动力减弱。

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