Acute pancreatitis-induced thrombotic thrombocytopenic purpura: A case report

Thrombotic thrombocytopenic purpura (TTP) is a life-threatening but treatable disorder. Acute pancreatitis is a well-described consequence of TTP, but TTP as a consequence of acute pancreatitis is rare. A 32-year-old male developed acute pancreatitis due to a fatty diet and suffered splenectomy 3 ye...

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Veröffentlicht in:World journal of clinical cases 2022-04, Vol.10 (12), p.3808-3813
Hauptverfasser: Wang, Chun-Hua, Jin, Hai-Feng, Liu, Wen-Ge, Guo, Ying, Liu, Zhen
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container_issue 12
container_start_page 3808
container_title World journal of clinical cases
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creator Wang, Chun-Hua
Jin, Hai-Feng
Liu, Wen-Ge
Guo, Ying
Liu, Zhen
description Thrombotic thrombocytopenic purpura (TTP) is a life-threatening but treatable disorder. Acute pancreatitis is a well-described consequence of TTP, but TTP as a consequence of acute pancreatitis is rare. A 32-year-old male developed acute pancreatitis due to a fatty diet and suffered splenectomy 3 years ago due to trauma. From day 4 of his onset of pain the blood examination showed the platelet extremely reduced, bilirubin elevated and creatinine increased. High clinical suspicion of TTP was made and prompt initiation of plasma exchange was given followed intravenous drip methylprednisolone. After 7 sessions of plasm exchange and the laboratory parameters were back to normal and the patient was discharged from the hospital on the 13 day of admission. Patients develop acute pancreatitis with no apparent causes for hemolytic anemia and thrombocytopenia, the possibility of TTP should be considered. Treatments for TTP including plasm exchange should be evaluated as soon as a diagnosis is made.
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Acute pancreatitis is a well-described consequence of TTP, but TTP as a consequence of acute pancreatitis is rare. A 32-year-old male developed acute pancreatitis due to a fatty diet and suffered splenectomy 3 years ago due to trauma. From day 4 of his onset of pain the blood examination showed the platelet extremely reduced, bilirubin elevated and creatinine increased. High clinical suspicion of TTP was made and prompt initiation of plasma exchange was given followed intravenous drip methylprednisolone. After 7 sessions of plasm exchange and the laboratory parameters were back to normal and the patient was discharged from the hospital on the 13 day of admission. Patients develop acute pancreatitis with no apparent causes for hemolytic anemia and thrombocytopenia, the possibility of TTP should be considered. 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title Acute pancreatitis-induced thrombotic thrombocytopenic purpura: A case report
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