Refractory Thrombotic Thrombocytopenic Purpura: A Case ReportCorrespondence Address :
Dr. Prabu Pandurangan,
Greams Road, Apollo Hospital, Chennai-600001, Tamil Nadu, India.
Thrombotic thrombocytopenic purpura is a thrombotic microangiopathy. Clinical manifestations occur due to decreased perfusion to the internal organs. Usually it responds to pulse steroids and plasma exchange. Various therapies are available for refractory cases which respond to N-Acetyl cysteine, cyclosporin, rituximab, bortezomib and caplacizumab. We report a case of refractory Thrombotic Thrombocytopenic Purpura (TTP) in a 29-years-old female showed improvement with the use of rituximab (anti-CD 20 monoclonal antibody), who presented with history of fever and one episode of seizure.
N-Acetyl cysteine, Rituximab, Splenectomy
Mohammed Shafi Abdulsalam, Venkateshwaran Radhakrishnan, Prabu Pandurangan. REFRACTORY THROMBOTIC THROMBOCYTOPENIC PURPURA: A CASE REPORT. Journal of Clinical and Diagnostic Research [serial online] 2018 March [cited: 2019 Jan 19 ]; 12:OD01-OD02. Available from
Date of Submission: Mar 18, 2017
Date of Peer Review: May 17, 2017
Date of Acceptance: Jan 16, 2018
Date of Publishing: Mar 01, 2018
FINANCIAL OR OTHER COMPETING INTERESTS: None.
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