Recognizing and managing hereditary and acquired thrombotic thrombocytopenic purpura in infants and children

We describe how infants and children with hereditary and acquired autoimmune thrombotic thrombocytopenic purpura (TTP) initially present and how they can be promptly diagnosed and effectively managed. These are uncommon disorders that are commonly misdiagnosed and can be rapidly fatal. TTP is caused by a severe deficiency of the plasma protease, A disintegrin and Metalloprotease with a ThromboSpondin type 1 motif, member 13 (ADAMTS13). Measurement of ADAMTS13 activity is becoming easily accessible. A common presentation of hereditary TTP is neonatal severe hemolysis and hyperbilirubinemia. However, the median age of diagnosis is not until 5.5 years. Plasma is effective treatment for exacerbations and for prophylaxis. Plasma may be replaced by recombinant ADAMTS13 when it becomes available. Acquired TTP is more frequent in older children, in whom it is more common in girls and is commonly associated with systemic lupus erythematosus. For acquired TTP, plasma exchange and immunosuppression are the current treatment for acute episodes; caplacizumab is now commonly used in adults and may replace plasma exchange.

Automated summary

This article describes the presentation, diagnosis, and treatment of infants and children with hereditary and acquired autoimmune thrombotic thrombocytopenic purpura (TTP). Plasma and recombinant ADAMTS13 are effective treatments for exacerbations, while plasma exchange and immunosuppression are common for acquired TTP, with caplacizumab emerging as a potential replacement for plasma exchange.