SciELO - Scientific Electronic Library Online

vol.58 número3Severe cutaneous adverse reactions (SCAR) syndromesEndometrial carcinoma: treatment índice de autoresíndice de materiabúsqueda de artículos
Home Pagelista alfabética de revistas  

Servicios Personalizados




Links relacionados


Revista da Associação Médica Brasileira

versión impresa ISSN 0104-4230

Rev. Assoc. Med. Bras. vol.58 no.3 São Paulo mayo/un. 2012 



Nephrocalcinosis in a patient with Sjögren's syndrome/systemic lupus erythematosus



Amanda Carolina Damasceno ZanutoI; Tatiara BuenoI; Vinicius Daher Alvares DelfinoII; Altair Jacob MocelinII

INephrology Residents, Hospital Evangélico de Londrina, Londrina, PR, Brazil
IINephrology Department, Hospital Evangélico de Londrina, Londrina, PR, Brazil

Correspondence to



A 46-year-old white woman has been followed in this nephrology clinic since 1995 due to recurrent nephrolithiasis and medullary nephrocalcinosis resulting from renal tubular acidosis (urinary pH of 8 in the context of systemic normal anion gap acidosis; serum potassium at lower limit, and 24-hour urine with normocalciuria but no detectable citrate) due to Sjögren's syndrome (SS). During follow-up, her adherence to alkali therapy had been suboptimal due to gastric intolerance to Shohl's solution, potassium citrate, and sodium bicarbonate. As consequence, she had progression in her nephrocalcinosis and passed several urinary calculi (biochemical analysis showed them to be composed of calcium phosphate and calcium oxalate). Currently, she presents normal estimated GFR (MDRD, 82 mL/min/1.73 m2) and no significant proteinuria, despite having presented, ten years after the diagnosis of SS, onset of systemic lupus erythematosus (SLE) with severe diffuse proliferative class IV lupus nephritis, treated successfully with corticosteroids and intravenous ciclophosphamide. Figure 1 shows the radiological appearance and Figure 2 depicts the ultrasonographic aspect of the patient's nephrocalcinosis.





Nephrocalcinosis is characterized by the presence of calcium deposits in the renal parenchyma; nephrolithiasis represents calcification within the lumen of the collecting system, ureter, and bladder1. Recent observation suggests that nephrocalcinosis and calcium nephrolithiasis are to be considered independent pathologies, and that nephrocalcinosis may cause calcium nephrolithiasis only in certain conditions2. Both types of renal calcification may be present in patients with SS. Nephrocalcinosis may be classified as cortical or medullary, according to the anatomic area involved3. When associated with SS, it is typically medullary and secondary to distal renal tubular acidosis (RTA). It is believed that the renal acidification problem seen in patients with SS is due to immunemediated loss of proton regulation4. In addition to RTA, other disorders such as hyperparathyroidism, medullary sponge kidney, renal papillary necrosis, renal tuberculosis, hyperoxaluria, milk-alkali syndrome, sarcoidosis, immobilization, and other conditions associated with hypercalcemia and hypercalciuria, may cause medullary nephrocalcinosis.

Nephrocalcinosis is usually identifiable by X-ray, but both ultrasonography (US) and computed tomography (CT) can detect it earlier than ordinary abdominal X-ray1. US is considered to be an excellent diagnostic method for detection and monitoring of nephrocalcinosis3. The finding of hyperchogenic pyramids with a normally echogenic cortex is believed to be specific to medullary nephrocalcinosis3,5. Despite being an excellent diagnostic method as well, CT (usually performed without radiocontrast) involves a considerable dose of radiation, which may limit its use for the follow-up of patients with nephrocalcinosis. Indeed, CT was found to be unnecessary for the clinical management of the patient.

Finally, the importance of investigating SS in patients with medullary nephrocalcinosis or nephrolithiasis associated with renal tubular acidosis, especially women, regardless of the presence of keratitis sicca or systemic symptoms, is emphasized, because it may be the first manifestation of the syndrome. Therapy for correction of acidosis is intended to control the nephrocalcinosis and preserve renal function6. This case corroborates that although RTA is a treatable urologic condition, incomplete treatment can lead to progression of nephrocalcinosis.



1. Vanrenterghem Y, Kuypres D, Verswijvel G, Schepens D. Renal cortical nephrocalcinosis. Nephrol Dial Transplant. 2000;15:1080-2.         [ Links ]

2. Vervaet BA, Verhulst A, D'Haese PC, De Broe ME. Nephrocalcinosis: new insights into mechanisms and consequences. Nephrol Dial Transplant. 2009;24: 2030-5.         [ Links ]

3. Hoppe B, Kemper MJ. Diagnostic examination of the child with urolithiais or nephrocalcinosis. Pediatr Nephrol. 2010;25:403-13.         [ Links ]

4. Evan AP, Lingeman J, Coe F, Shao Y, Miller N, Matlaga B, et al. Renal histopathology of stone-forming patients with distal renal tubular acidosis. Kidney Int. 2007;71:795-801.         [ Links ]

5. Simões A, Domingos F, Prata MM. Nephrocalcinosis induced by furosemide in an adult patient with incomplete renal tubular acidosis. Nephrol Dial Transplant. 2001;16:1073-4.         [ Links ]

6. Soriano JR. Renal tubular acidosis: the clinical entity. J Am Soc Nephrol. 2002;13:2160-70.         [ Links ]



Correspondence to:
Vinicius D. A. Delfino
Departamento de Nefrologia, Centro de Ciências da Saúde, Universidade Estadual de Londrina
Av. Robert Koch, 60 Vila Operária
86038-440, Londrina - PR, Brazil



Study conducted at Universidade Estadual de Londrina, Londrina, PR, Brazil

Creative Commons License Todo el contenido de esta revista, excepto dónde está identificado, está bajo una Licencia Creative Commons