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代谢性骨病中的肾脏超声检查。

Renal ultrasound in metabolic bone disease.

作者信息

Jequier S, Cramer B, Goodyer P, Kronick J, Reade T

出版信息

Pediatr Radiol. 1986;16(2):135-9. doi: 10.1007/BF02386638.

DOI:10.1007/BF02386638
PMID:3513110
Abstract

Fifty-one patients aged 1 year to 56 years with metabolic bone disease underwent renal ultrasound. Medullary nephrocalcinosis was found in nine of 24 patients with X-linked hypophosphatemic rickets and is considered to be iatrogenic, related to vitamin D therapy. Another three in this group of 24 with both medullary and cortical increased renal echogenicity had suffered from repeated episodes of vitamin D intoxication and had secondary hyperparathyroidism. Nephrocalcinosis was less frequent in patients with treated vitamin D-dependent rickets or hypophosphatemic bone disease where generally smaller doses of vitamin D are given. Patients with pseudohypoparathyroidism, on small doses of vitamin D, had a normal renal ultrasound. In cystinosis and Fanconi's syndrome, the kidneys are small, echodense (both the cortex and medulla) with a tendency to cyst formation.

摘要

51例年龄在1岁至56岁之间患有代谢性骨病的患者接受了肾脏超声检查。在24例X连锁低磷性佝偻病患者中,有9例发现了髓质肾钙质沉着症,被认为是医源性的,与维生素D治疗有关。在这24例同时存在髓质和皮质肾回声增强的患者中,另外3例曾反复发生维生素D中毒并患有继发性甲状旁腺功能亢进。在接受治疗的维生素D依赖性佝偻病或低磷性骨病患者中,肾钙质沉着症的发生率较低,这些患者通常给予较小剂量的维生素D。接受小剂量维生素D治疗的假性甲状旁腺功能减退患者肾脏超声检查结果正常。在胱氨酸病和范科尼综合征中,肾脏较小,回声增强(皮质和髓质均如此),并有形成囊肿的倾向。

相似文献

1
Renal ultrasound in metabolic bone disease.代谢性骨病中的肾脏超声检查。
Pediatr Radiol. 1986;16(2):135-9. doi: 10.1007/BF02386638.
2
Nephrocalcinosis and its relationship to treatment of hereditary rickets.
J Pediatr. 1987 Nov;111(5):700-4. doi: 10.1016/s0022-3476(87)80245-7.
3
Effects of therapy in X-linked hypophosphatemic rickets.X连锁低磷血症性佝偻病的治疗效果
N Engl J Med. 1991 Dec 26;325(26):1843-8. doi: 10.1056/NEJM199112263252604.
4
[Iliac crest biopsies in various forms of rickets].[不同类型佝偻病的髂嵴活检]
Monatsschr Kinderheilkd (1902). 1974 Jul;122(7):586-7.
5
Healing of bone disease in X-linked hypophosphatemic rickets/osteomalacia. Induction and maintenance with phosphorus and calcitriol.X连锁低磷性佝偻病/骨软化症中骨病的治疗。磷和骨化三醇的诱导与维持治疗。
J Clin Invest. 1985 Jun;75(6):1858-68. doi: 10.1172/JCI111900.
6
Nephrocalcinosis.肾钙质沉着症
Curr Opin Pediatr. 1997 Apr;9(2):160-5.
7
Hyperoxaluria is not a cause of nephrocalcinosis in phosphate-treated patients with hereditary hypophosphatemic rickets.高草酸尿症并非接受磷酸盐治疗的遗传性低磷性佝偻病患者肾钙质沉着症的病因。
Nephron. 1993;64(4):526-31. doi: 10.1159/000187395.
8
[Hypophosphatemia of a genetic origin].[遗传性低磷血症]
Nephrologie. 1992;13(3):115-21.
9
[Vitamin D in the prevention of growth disorders].[维生素D在预防生长障碍中的作用]
Acta Vitaminol Enzymol. 1980;2(3-4):87-94.
10
Hereditary hypophosphatemic rickets with hypercalciuria: case report.遗传性低血磷性佝偻病伴高钙尿症:病例报告。
Nefrologia. 2012 Jul 17;32(4):529-34. doi: 10.3265/Nefrologia.pre2012.Apr.11321.

引用本文的文献

1
Nephrocalcinosis in X-linked hypophosphatemia: effect of treatment versus disease.
Pediatr Nephrol. 1995 Apr;9(2):173-5. doi: 10.1007/BF00860736.
2
Hypercalciuria and ultrasound abnormalities in children with cystinosis.胱氨酸病患儿的高钙尿症和超声异常
Pediatr Nephrol. 1995 Feb;9(1):45-7. doi: 10.1007/BF00858968.
3
Update on nephropathic cystinosis.肾性胱氨酸病的最新进展。
Pediatr Nephrol. 1990 Nov;4(6):645-53. doi: 10.1007/BF00858644.

本文引用的文献

1
Nephrocalcinosis in radiographs, computed tomography, sonography and histology.
Pediatr Radiol. 1980;9(1):19-26. doi: 10.1007/BF00973964.
2
X-linked hypophosphatemia: effect of calcitriol on renal handling of phosphate, serum phosphate, and bone mineralization.X连锁低磷血症:骨化三醇对肾脏磷处理、血清磷及骨矿化的影响。
J Clin Endocrinol Metab. 1981 Mar;52(3):463-72. doi: 10.1210/jcem-52-3-463.
3
Sonographic diagnosis of furosemide-induced nephrocalcinosis in newborn infants.
J Ultrasound Med. 1984 Dec;3(12):553-6. doi: 10.7863/jum.1984.3.12.553.
4
Response to crystalline 1alpha-hydroxyvitamin D3 in vitamin D dependency.
Pediatr Res. 1975 Jul;9(7):593-9. doi: 10.1203/00006450-197507000-00008.
5
Hypophosphatemic nonrachitic bone disease: an entity distinct from X-linked hypophosphatemia in the renal defect, bone involvement, and inheritance.低磷性非佝偻病性骨病:一种在肾脏缺陷、骨骼受累及遗传方面与X连锁低磷血症不同的疾病实体。
Am J Med Genet. 1977;1(1):101-17. doi: 10.1002/ajmg.1320010111.