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DOI 10.1177/120347540100500108

Медицинская библиотека · Journal of cutaneous medicine and surgery · 2001

Eosinophilic fasciitis occurring four weeks after the onset of dialysis in a renal failure patient.

Florell S R, Egan C A, Gregory M C, Zone J J, Petersen M J

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Аннотация

BACKGROUND

Eosinophilic fasciitis is a rare, scleroderma-like disease that usually affects the extremities of young to middle-aged males. The disease may cause flexion contractures and limit joint mobility and is associated with peripheral eosinophilia. The fascia, by definition, is infiltrated with mononuclear cells and typically with eosinophils. Eosinophilic fasciitis may be separated from another sclerodermatous disorder, linear scleroderma, by its response to systemic corticosteroids. The etiology is unclear but eosinophilic fasciitis has numerous disease associations. However, it has not previously been associated with renal failure and hemodialysis.

OBJECTIVE

This article reports a case of eosinophilic fasciitis occurring four weeks following the onset of hemodialysis.

METHODS

The clinical and histologic features confirmed the diagnosis of eosinophilic fasciitis. He was treated with systemic corticosteroids with good response.

CONCLUSION

This is the first reported patient who developed eosinophilic fasciitis in close temporal relationship with the start of hemodialysis. While eosinophilic fasciitis may be coincidental with a common disorder, namely, renal failure, it is interesting to note that hemodialysis patients often have immune-regulation abnormalities and peripheral eosinophilia.

Для цитирования: Florell S R, Egan C A, Gregory M C, Zone J J, Petersen M J. Eosinophilic fasciitis occurring four weeks after the onset of dialysis in a renal failure patient.. Journal of cutaneous medicine and surgery. 2001. DOI: 10.1177/120347540100500108.

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