Improvement of Erdheim-Chester disease-related renal failure after treatment with anakinra

Abstract Erdheim-Chester disease (ECD) is a rare non-Langerhans cell histiocytosis characterized by infiltrates of lipid-laden CD68+ /CD1a− histiocytes, affecting heart, lungs, central nervous system, and bones. Kidney and adjacent structures can also be affected, leading to renal failure in about 3...

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Veröffentlicht in:Kidney research and clinical practice 2014, 33(3), , pp.165-167
Hauptverfasser: Podestà, Manuel Alfredo, Graziani, Giorgio, Reggiani, Francesco, Buemi, Michele, Badalamenti, Salvatore, Ponticelli, Claudio
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Sprache:eng
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Zusammenfassung:Abstract Erdheim-Chester disease (ECD) is a rare non-Langerhans cell histiocytosis characterized by infiltrates of lipid-laden CD68+ /CD1a− histiocytes, affecting heart, lungs, central nervous system, and bones. Kidney and adjacent structures can also be affected, leading to renal failure in about 30% of cases. The diagnosis is challenging, and treatment is generally based on administration of interferon-alpha (IFNα), but preliminary results also showed the therapeutic efficacy of anakinra, an antagonist of the receptor of interleukin-1 (IL-1). We report the case of an elderly patient with ECD and severe involvement of the heart and kidneys who was successfully treated with anakinra.
ISSN:2211-9132
2211-9140
DOI:10.1016/j.krcp.2014.07.007