• Title of article

    Cutaneous amyloidosis as the first presentation of Waldenstrom macroglobulinemia

  • Author/Authors

    Rafiei, Rana Skin Research Center, Department of Dermatology - Razi Hospital - School of Medicine - Guilan University of Medical Sciences, Rasht, Iran , Eftekhari, Hojat Skin Research Center - Department of Dermatology, Razi Hospital - School of Medicine - Guilan University of Medical Sciences, Rasht, Iran , Rafiee, Behnam Department of Pathology - NYU Winthrop Hospital, USA

  • Pages
    3
  • From page
    340
  • To page
    342
  • Abstract
    Waldenstrom macroglobulinemia is a lymphoplasmacytic lymphoma with elevated serum immunoglobulin M and multi-organ involvement. Primary systemic amyloidosis usually develops due to immunoglobulin light chains depositions in different organs due to an underlying gammopathy. Case presentation: Our patient was an 86-year-old man with macroglossia, ecchymotic patches and bullous lesions associated with a skin laxity on the periorbital, palmar, and glans penis areas. Skin biopsy confirmed dermal amyloid depositions. In serum immunofixation electrophoresis, prominent monoclonal immunoglobulin-M lambda light chains were detected associated with prominent lymphoplasmacytic infiltration in bone marrow biopsy which was diagnosed as Waldenstrom macroglobulinemia. Conclusion: Skin involvement presenting as cutaneous amyloidosis could be the first manifestation of Waldenstrom macroglobulinemia. We should think about an underlying gammopathy in an old patient with skin laxity and ecchymosis.
  • Keywords
    Primary systemic , amyloidosis , Waldenstrom macroglobulinemia
  • Journal title
    Caspian Journal of Internal Medicine (CJIM)
  • Serial Year
    2020
  • Record number

    2631605