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Severe immune thrombocytopenia in two patients with systemic sclerosis
Gonçalo Boleto1, Jérôme Avouac2, Bertrand Godeau3
1Department of Rheumatology, université Paris Cité, Cochin Hospital, Paris, France.
Immune thrombocytopenia (ITP) is rare in systemic sclerosis (SSc). This report details two severe ITP cases in SSc patients, highlighting treatment challenges and successful interventions like splenectomy and novel therapies.
Area of Science:
- Hematology
- Rheumatology
- Immunology
Background:
- Thrombocytopenia in systemic sclerosis (SSc) is uncommon and often suggests scleroderma renal crisis.
- Immune thrombocytopenia (ITP), while common in systemic lupus erythematosus, is exceptionally rare in SSc patients.
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