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NDT Advance Access originally published online on June 30, 2007
Nephrology Dialysis Transplantation 2007 22(10):3094; doi:10.1093/ndt/gfm435
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© The Author [2007]. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org



Treatment with corticosteroids does not seem to benefit nephrogenic systemic fibrosis

Email: herwigpi{at}yahoo.com

Sir,

Nephrogenic systemic fibrosis (NSF) is a formerly unknown disease, which has become more and more recognized. It affects patients with kidney failure and, to a great extent, mimics systemic sclerosis [1]. An association between NSF and magnetic resonance image with gadolinium-based contrast agents has been suggested [2]. Herein, we report a case of NSF, in which corticosteroids were administered at the very beginning of the disease.

A 62-year-old male haemodialysis patient abruptly developed symmetrical painful, oedematous swelling of the skin on his fingers and palms. In addition, the swollen tissue around the palmar flexor tendons resembled tendovaginitis. The range of motion of the fingers was severely limited and painful. The patient received NSAIDs, but the symptoms persisted. Therefore, and because the disease was believed to be an inflammatory condition, the patient was treated with 50 mg prednisolone daily. However, swelling and pain did not improve. In the following weeks, the dosage of prednisolone was slowly tapered and finally discontinued after 2 months. As time passed, the oedematous swelling gradually resolved, but in parallel, the tissue became more and more fibrotic. After 1 year, the patient had contractions of his fingers, toes, elbows and knees (Figure 1). Given the course of the disease, we retrospectively recognized this condition to be NSF. Notably, 7 days before the start of symptoms, the patient had an MR angiography. The diagnosis was finally verified with a skin biopsy. The histological examination revealed large amounts of fibroblastic tissue, containing numerous CD34-positive fibroblasts [3].


Figure 1
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Fig. 1. Contractions of the fingers in nephrogenic systemic fibrosis.

 
NSF is a debilitating and sometimes fatal disease, affecting the skin, muscle, and internal organs [1,2]. These days, no consistently successful treatment exists. Because of their anti-oedematous and anti-fibrotic properties, corticosteroids may theoretically be helpful in the treatment of NSF. Given the ineffectiveness of prednisolone in our patient with regard to swelling, pain and progression of the disease, we believe that corticosteroids neither ameliorate the symptoms nor are they of benefit in the evolution of NSF.

Conflict of interest statement. None declared.

Herwig Pieringer, Bernhard Schmekal, Othmar Janko and Georg Biesenbach

Section of Rheumatology
and Section of Nephrology,
2nd Department of Medicine,
General Hospital Linz,
Krankenhausstr. 9, A-4020 Linz,
Austria

Notes

See http://www.oxfordjournals.org/our_journals/ndtplus/

References

  1. Galan A, Cowper SE, Bucala R. Nephrogenic systemic fibrosis (nephrogenic fibrosing dermopathy). Curr Opin Rheumatol (2006) 18:614–617.[Web of Science][Medline]
  2. http://www.fda.gov/cder/drug/InfoSheets/HCP/gcca_200705.htm.
  3. Cowper SE, Su LD, Bhawan J, Robin HS, LeBoit PE. Nephrogenic fibrosing dermopathy. Am J Dermatopathol (2001) 23:383–393.[CrossRef][Web of Science][Medline]

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