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Published on: October 12, 2012
Cryoglobulinaemic leg ulcers associated with transient ischaemic attack
1Sisli Etfal Training and Research Hospital, Istanbul, Turkey. ialtunay@gmail.com
Insights
This case study highlights a patient with non-healing leg ulcers and transient ischemic attack, diagnosed with cryoglobulinemia type I. Treatment with steroids and anticoagulants successfully healed the ulcers.
Area of Science:
- Dermatology
- Rheumatology
- Hematology
Background:
- Cryoglobulinemia type I is a rare condition characterized by monoclonal immunoglobulins causing hyperviscosity.
- It can manifest with diverse clinical symptoms, including skin lesions and vascular events.
Observation:
- An 87-year-old male presented with non-healing leg ulcers and transient ischemic attack.
- Positive serum cryoglobulins and monoclonal IgG-kappa were detected.
- Histopathology revealed leukocytoclastic vasculitis with fibrinoid deposition.
Findings:
- Direct immunofluorescence confirmed vasculitis with immunoglobulin and complement deposition.
- The patient was diagnosed with cryoglobulinemia type I without an underlying disease.
- Successful treatment of leg ulcers was achieved with high-dose steroids and anticoagulants.
Implications:
- This case underscores the importance of considering cryoglobulinemia type I in patients with unexplained leg ulcers and vascular symptoms.
- Early diagnosis and appropriate management, including immunosuppression and anticoagulation, can lead to favorable outcomes.
- Further research into the pathogenesis and treatment of cryoglobulinemia type I is warranted.
Abstract:
This study report an 87-year-old male patient with multiple, superficial non-healing leg ulcers and transient ischaemic attack. Testing for serum cryoglobulins returned positive and for serum immunofixation electrophoresis displayed increased monoclonal IgG-kappa. Histological examination revealed epidermis ulceration, accumulations of neutrophils with nuclear dust or debris (leukocytoclasia) and PAS positive homogen eosinophilic fibrin deposition in the vessel wall. Leucocytoclastic vasculitis was diagnosed pathologically. Direct immunofluorescence testing was performed for confirmation of the diagnosis of cutaneous vasculitis, with intravascular deposition of IgA, IgG, IgM and C3 in the walls of vessels of papillary and reticular dermis. There was no underlying disease and the patient was diagnosed with cryoglobulinaemia type I. Leg ulcers responded successfully to treatment with high dose steroids and anticoagulant agents and healed within 2 months.
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