Osteomalacia complicating renal tubular acidosis in association with sjogren’s syndrome

المؤلفون المشاركون

Bin Maiz, Hedi
Krid, Madihah
al-Ati, Zahrah
Rayyis, Lamya
Zouaghi, Karim
Boulahya, Ghadah
Bin Fatimah, Layla
Beji, Sumayyah
Bin Musa, Fatimah
Samawi, Wided

المصدر

Saudi Journal of Kidney Diseases and Transplantation

العدد

المجلد 25، العدد 5 (31 أكتوبر/تشرين الأول 2014)، ص ص. 1072-1077، 6ص.

الناشر

المركز السعودي لزراعة الأعضاء

تاريخ النشر

2014-10-31

دولة النشر

السعودية

عدد الصفحات

6

التخصصات الرئيسية

الطب البشري

الموضوعات

الملخص EN

Renal involvement in Sjogren’s syndrome (SS) is not uncommon and may precede other complaints.

Tubulointerstitial nephritis is the most common renal disease in SS and may lead to renal tubular acidosis (RTA), which in turn may cause osteomalacia.

Nevertheless, osteomalacia rarely occurs as the first manifestation of a renal tubule disorder due to SS.

We herewith describe a 43-year-old woman who was admitted to our hospital for weakness, lumbago and inability to walk.

X-ray of the long bones showed extensive demineralization of the bones.

Laboratory investigations revealed chronic kidney disease with serum creatinine of 2.3 mg / dL and creatinine clearance of 40 mL / min, hypokalemia (3.2 mmol / L), hypophosphatemia (0.4 mmol / L), hypocalcemia (2.14 mmol / L) and hyperchloremic metabolic acidosis (chlorine : 114 mmol / L ; alkaline reserve : 14 mmol / L).

The serum alkaline phosphatase levels were elevated.

The serum levels of 25-hydroxyvitamin D and 1,25-dihydroxy vitamin D were low and borderline low, respectively, and the parathyroid hormone level was 70 pg / L.

Urinalysis showed inappropriate alkaline urine (urinary PH : 7), glycosuria with normal blood glucose, phosphaturia and uricosuria.

These values indicated the presence of both distal and proximal RTA.

Our patient reported dryness of the mouth and eyes and Schirmer’s test showed xerophthalmia.

An accessory salivary gland biopsy showed changes corresponding to stage IV of Chisholm and Masson score.

Kidney biopsy showed diffuse and severe tubulo-interstitial nephritis with dense lymphoplasmocyte infiltrates.

Sicca syndrome and renal interstitial infiltrates indicated SS as the underlying cause of the RTA and osteomalacia.

The patient received alkalinization, vitamin D (Sterogyl®), calcium supplements and steroids in an initial dose of 1 mg / kg / day, tapered to 10 mg daily.

The prognosis was favorable and the serum creatinine level was 1.7 mg / dL, calcium was 2.2 mmol / L and serum phosphate was 0.9 mmol / L.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

al-Ati, Zahrah& Bin Fatimah, Layla& Boulahya, Ghadah& Rayyis, Lamya& Krid, Madihah& Samawi, Wided…[et al.]. 2014. Osteomalacia complicating renal tubular acidosis in association with sjogren’s syndrome. Saudi Journal of Kidney Diseases and Transplantation،Vol. 25, no. 5, pp.1072-1077.
https://search.emarefa.net/detail/BIM-400459

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

al-Ati, Zahrah…[et al.]. Osteomalacia complicating renal tubular acidosis in association with sjogren’s syndrome. Saudi Journal of Kidney Diseases and Transplantation Vol. 25, no. 5 (2014), pp.1072-1077.
https://search.emarefa.net/detail/BIM-400459

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

al-Ati, Zahrah& Bin Fatimah, Layla& Boulahya, Ghadah& Rayyis, Lamya& Krid, Madihah& Samawi, Wided…[et al.]. Osteomalacia complicating renal tubular acidosis in association with sjogren’s syndrome. Saudi Journal of Kidney Diseases and Transplantation. 2014. Vol. 25, no. 5, pp.1072-1077.
https://search.emarefa.net/detail/BIM-400459

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references : p. 1076-1077

رقم السجل

BIM-400459