nephrocalcinosis/náusea

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[Nephrocalcinosis associated with the use of anabolic steroid].

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The anabolic steroid have been used as a therapeutic tool in various clinical conditions. However, indiscriminate use associated with other nutritional supplements has generated serious adverse effects. METHODS Male, 21 years old, admitted with nausea, fatigue, appetite loss, headache and

A case of primary hyperparathyroidism with hypercalcemic nephropathy in children.

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Primary hyperparathyroidism is a rare disease in children and is characterized by conspicuous skeletal and renal changes. A 12 year old male patient presented with symptoms of polydipsia, polyuria, general weakness, nausea, and vomiting which had begun 3 months earlier, and showed typical laboratory

Renal failure due to acute phosphate nephropathy.

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Case report of a 62-year-old woman who developed acute renal failure due to nephrocalcinosis, also called acute phosphate nephropathy, after large bowel cleansing in preparation for colonoscopy using oral sodium phosphate solution (Phosphoral, de Witt, Cheshire, UK). Subsequently her renal

Successful Management of Refractory Type 1 Renal Tubular Acidosis with Amiloride.

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A 28-year-old female with history of hypothyroidism, Sjögren's Syndrome, and Systemic Lupus Erythematosus (SLE) presented with complaints of severe generalized weakness, muscle pain, nausea, vomiting, and anorexia. Physical examination was unremarkable. Laboratory test showed hypokalemia at 1.6

Conservative Management of a Gestational Hypercalcemia Due to Primary Hyperparathyroidism with Lack of Complications

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Introduction: Primary hyperparathyroidism (PHPT) is rare in pregnancy. PHPT and hypercalcemia are associated with negative maternofetal outcomes. Therefore, an early diagnosis and an adequate treatment are essential.

Immobilization hypercalcemia in spinal cord injury.

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Four patients having high-level quadriplegia developed elevated serum calcium concentrations (11 to 15.8 mg/100 ml) within three months of injury. All were young males (ages 15 to 19 years) and quadriplegic (C4-C7). Presenting symptoms were nausea, vomiting, polydipsia, polyuria and lethargy. In two

Treatment of acute lymphoblastic leukemia-induced extreme hypercalcemia with pamidronate and calcitonin.

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OBJECTIVE To describe extreme hypercalcemia as the presenting feature of acute lymphoblastic leukemia in an 8-yr-old girl and the combined use of pamidronate and calcitonin for its treatment. METHODS Case report. METHODS Pediatric intensive care unit. METHODS An 8-yr-old girl with 20.0 mg/dL serum

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