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Case 371 |
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The patient is a 33-year-old male, with a previous history of multiple renal calculi since childhood, with spontaneous and surgical passing. He was admitted for a new surgical procedure, when medical evaluation was requested, revealing hypocalcemia, hypophosphatemia and metabolic acidosis. He denied having used prescription or recreational drugs. A plain abdominal radiograph was performed, in supine position, anteroposterior projection (images 1 and 2). |
Given the medical history and images presented, what is the most prominent abnormality in this patient’s renal parenchyma? |
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a) Nephrolithiasis 25% |
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b) Renal scar 25% |
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c) Nephrocalcinosis 25% |
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d) Polycystic kidneys 25% |
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Image 1 – Plain abdominal radiograph, in supine position, anteroposterior projection. Multiple calcifications (highlighted by the green line) are seen grouped in the renal topography; the kidneys measure approximately 10 x 4 cm in the longitudinal and transverse axes, respectively.
Image 2 – Plain abdominal radiograph, in supine position, anteroposterior projection (negative image). Multiple calcifications (highlighted by the green line) are seen grouped in the renal topography.
-RTA is a result of malfunctioning of the renal tubules responsible for HCO³- reabsorption (proximal RTA) or H+ excretion (distal RTA);
-RTA should be suspected in the presence of a hyperchloremic metabolic acidosis, with a normal anion gap;
-Urinary pH greater than 5.5 in patients with a normal anion gap is characteristic of distal RTA;
-When treating distal RTA, the goal is not only to correct biochemical abnormalities, but also to prevent progression of nephrocalcinosis and prevent chronic renal failure;
-In RTA, the prognosis is directly related to early diagnosis.
- Cheidde L, Ajzen SA, Tamer Langen CH, et al. A critical appraisal of the radiological evaluation of nephrocalcinosis. Nephron Clin Pract 2007; 106:c119.
- Piccoli GB, De Pascale A, Randone O, et al. Revisiting nephrocalcinosis: A single-centre perspective. A northern Italian experience. Nephrology (Carlton) 2016; 21:97.
- Blanchard A, Bockenhauer D, Bolignano D, et al. Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference. Kidney Int 2017; 91:24.
- Schepens D, Verswijvel G, Kuypers D, Vanrenterghem Y. Images in Nephrology. Renal cortical nephrocalcinosis. Nephrol Dial Transplant 2000; 15:1080.
- Wrong O. Nephrocalcinosis. In: Oxford Textbook of Clinical Nephrology, Davison AM, Cameron JS, Grünfeld J, et al (Eds), Oxford University Press, Oxford 2005. p.1375.
- Soriano, JR. Renal Tubular Acidosis: The Clinical Entity. JASN Aug 2002, 13 (8) 2160-2170;
Luiz Gustavo de Faria Ferreira, 5th year medical student at UFMG.
Mail: gustavoff96[at]gmail.com
Dr. Lilian Pires de Freitas do Carmo, nephrologist and assistant professor at the Faculdade de Medicina at UFMG.
Mail: lilianpfreitas[at]yahoo.com.br
Dr. Cécil Bruno Buldrini Filogônio, professor at the Department of Anatomy and Imaging at UFMG.
Mail: cecilbruno[at]gmail.com
Gabriella Shiomatsu, Felipe Eduardo Fagundes Lopes, Larissa Rezende, Maria Cecília Nassif, professor José Nelson Mendes Vieira.
Rafael Antonio Teixeira Malta, 6th year medical student at UFMG
Mail: rafaelmalta148[at]gmail.com
(Municipal Health Secretary – Piracicaba, São Paulo) Metabolic acidosis is the excess of acidity in the blood, characterized by an abnormally low bicarbonate concentration. In the clinical evaluation of acid-base disorders, the differential diagnosis can be obtained by calculating the anion gap. Which of the disorders below can cause a normal anion gap metabolic acidosis? |
a) Distal (type 1) renal tubular acidosis 25% |
b) Ethylene glycol poisoning 25% |
c) Typical diabetic ketoacidosis 25% |
d) Salicylate poisoning 25% |
e) 25% |
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