Cytophagic histiocytic panniculitis in a 74-year-old man

Age Ageing. 2013 May;42(3):409-10. doi: 10.1093/ageing/aft034. Epub 2013 Mar 18.

Abstract

Cytophagic histiocytic panniculitis is a chronic histiocytic disease of the subcutaneous adipose tissue characterised by lobular panniculitis with histiocytes containing blood cell fragments. It is also associated with marked systemic features such as fever, pancytopenia, hepatosplenomegaly, liver abnormalities and coagulopathy. We report a case of cytophagic histiocytic panniculitis in a 74-year-old man successfully treated using combination therapy with prednisolone and cyclosporine A.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Cyclosporine / therapeutic use
  • Cytophagocytosis*
  • Drug Therapy, Combination
  • Gallium Radioisotopes
  • Glucocorticoids / therapeutic use
  • Histiocytosis / classification*
  • Histiocytosis / diagnosis
  • Histiocytosis / drug therapy
  • Humans
  • Immunosuppressive Agents / therapeutic use
  • Male
  • Methylprednisolone / therapeutic use
  • Panniculitis / classification*
  • Panniculitis / diagnosis
  • Panniculitis / drug therapy
  • Prednisolone / therapeutic use
  • Treatment Outcome
  • Whole Body Imaging

Substances

  • Gallium Radioisotopes
  • Glucocorticoids
  • Immunosuppressive Agents
  • Cyclosporine
  • Prednisolone
  • Methylprednisolone