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一例伴有1型肾小管性酸中毒的范科尼综合征病例。

A case of Fanconi syndrome with type 1 renal tubular acidosis.

作者信息

Sakai T, Suzuki J, Marumo F, Kikawada R

出版信息

Jpn Circ J. 1981 Oct;45(10):1164-9. doi: 10.1253/jcj.45.1164.

Abstract

A 32-year-old woman of Fanconi syndrome with disorders of amino acid, glucose, uric acid and phosphate reabsorption system in proximal tubule and of renal acid excretion mechanism in distal tubule was reported. By the ammonium chloride loading test, urinary pH could only be decreased by 5.9, and excretion rates of NH4+ and titratable acids were 18.9 and 31.1 mEq/min, respectively. In the bicarbonate loading test, net renal reabsorption of bicarbonate was 2.86 mEq/100 ml GFR when plasma bicarbonate concentration was 29 mEq/L, and threshold of bicarbonate excretion was 24-26 mEq/L. These results suggest that hydrogen ion excretion disorder in distal tubules exists, while bicarbonate reabsorption ability in proximal tubule is normal.

摘要

报道了一名32岁的范科尼综合征女性患者,其近端肾小管存在氨基酸、葡萄糖、尿酸和磷酸盐重吸收系统紊乱,远端肾小管存在肾酸排泄机制紊乱。通过氯化铵负荷试验,尿pH仅能降低5.9,NH4+和可滴定酸的排泄率分别为18.9和31.1 mEq/min。在碳酸氢盐负荷试验中,当血浆碳酸氢盐浓度为29 mEq/L时,肾脏对碳酸氢盐的净重吸收为2.86 mEq/100 ml GFR,碳酸氢盐排泄阈值为24 - 26 mEq/L。这些结果表明远端肾小管存在氢离子排泄障碍,而近端肾小管的碳酸氢盐重吸收能力正常。

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