Monoclonal Cryoglobulinemia Clinically Mimicking Leukocytoclastic Vasculitis: A Case Report and Literature Review
Monoclonal cryoglobulinemia commonly presents with cutaneous manifestations and develops almost exclusively in the setting of an underlying lymphoproliferative or hematologic disorder of B-cell lineage. Herein, we describe a case of a 48-year-old woman who presented with a recurrent and symmetric hemorrhagic papular eruption. Punch biopsy and direct immunofluorescence were consistent with monoclonal cryoglobulinemia. Systemic workup was notable for elevated kappa free light chains with a monoclonal immunoglobulin M kappa component on serum protein electrophoresis, and bone marrow biopsy was consistent with lymphoplasmacytic lymphoma.
Authors
- Taylor E. Arnoff (ORCID: https://orcid.org/0000-0001-7181-9417)
- Nicholas Gessner
- Dean David George (ORCID: https://orcid.org/0000-0001-6748-5020)
- Leslie Robinson‐Bostom (ORCID: https://orcid.org/0000-0001-6551-7762)
- Fatima N. Mirza (ORCID: https://orcid.org/0000-0003-1299-6258)
Institutions
- Hartford Hospital (US)
- Brown University (US)
- Hartford Financial Services (United States)
Publication Details
- Journal
- American Journal of Dermatopathology
- Published
- 2025-09-23
- DOI
- https://doi.org/10.1097/dad.0000000000003129
- Primary Topic
- Chronic Lymphocytic Leukemia Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00