Refractor y thrombotic thrombocytopenic pur pura following acute pancreatitis

Thrombotic thrombocytopenic purpura (TTP) is a rare blood disorder with an estimated incidence of 4–5 cases per million people per year. It is characterized by small-vessel platelet-rich thrombi that cause thrombocytopenia, microangiopathic hemolytic anemia and organ damage. There are reports in...

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Main Authors: Ebisa Bekele, Bethel Shiferaw, Alexandra Sokolova, Arpan Shah, Phillip Saunders, Alida Podrumar, Javed Iqbal
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2016-09-01
Series:Journal of Acute Disease
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2221618916301196
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spelling doaj-4dbc880e0f3f4911ae164f84e38d6aff2020-11-25T00:16:24ZengWolters Kluwer Medknow PublicationsJournal of Acute Disease2221-61892016-09-015543443610.1016/j.joad.2016.08.013Refractor y thrombotic thrombocytopenic pur pura following acute pancreatitisEbisa Bekele0Bethel Shiferaw1Alexandra Sokolova2Arpan Shah3Phillip Saunders4Alida Podrumar5Javed Iqbal6Department of Medicine, Nassau University Medical Center, East Meadow, New York, USADepartment of Medicine, Nassau University Medical Center, East Meadow, New York, USADepartment of Medicine, Nassau University Medical Center, East Meadow, New York, USADepartment of Medicine, Nassau University Medical Center, East Meadow, New York, USADepartment of Medicine, Nassau University Medical Center, East Meadow, New York, USADepartment of Medicine, Division of Hematology and Oncology, Nassau University Medical Center, East Meadow, New York, USADepartment of Medicine, Division of Pulmonary and Critical Care, Nassau University Medical Center, East Meadow, New York, USAThrombotic thrombocytopenic purpura (TTP) is a rare blood disorder with an estimated incidence of 4–5 cases per million people per year. It is characterized by small-vessel platelet-rich thrombi that cause thrombocytopenia, microangiopathic hemolytic anemia and organ damage. There are reports in literature that TTP and acute pancreatitis are associated, indicating each can be the cause of the other. However, acute pancreatitis triggering TTP is very rare. A 71 years old female presented with abdominal pain of 3 days, followed by dark urine. She had icteric sclera, petechial rash and mild epigastric tenderness. Lab findings were significant for hemolytic anemia, thrombocytopenia and elevated lipase. CT of abdomen showed evidence of pancreatitis and cholelithiasis. After admission, patient developed symptoms of stroke. Further investigation showed elevated lactate dehydrogenase and normal coagulation studied with peripheral blood smear showed 5–6 schistocytes/high power field. Disintegrin and metalloproteinase with thrombospondin motifs-13 (ADAMTS13) activity showed less than 3% with high ADAMTS13 inhibitor 2.2. Patient required 6–7 weeks of daily plasmapheresis until she showed complete response. Our patient presented with clinical features of pancreatitis prior to having dark urine and petechial rash. Therefore, we strongly believe that our patient had pancreatitis which was followed by TTP. Patient's ADMTS13 activity was 6% after 10 plasma exchanges, signifying refractory TTP and higher risk for morbidity and mortality. There are limited data and consensus on the management of refractory TTP. TTP and acute pancreatitis are associated. However, refractory TTP following acute pancreatitis is rarely mentioned in the literature. We would like to emphasize the importance of having higher clinical suspicion of the association of both disease entities.http://www.sciencedirect.com/science/article/pii/S2221618916301196Thrombotic thrombocytopenicpurpuraAcute pancreatitisRefractoryPlasmapheresis
collection DOAJ
language English
format Article
sources DOAJ
author Ebisa Bekele
Bethel Shiferaw
Alexandra Sokolova
Arpan Shah
Phillip Saunders
Alida Podrumar
Javed Iqbal
spellingShingle Ebisa Bekele
Bethel Shiferaw
Alexandra Sokolova
Arpan Shah
Phillip Saunders
Alida Podrumar
Javed Iqbal
Refractor y thrombotic thrombocytopenic pur pura following acute pancreatitis
Journal of Acute Disease
Thrombotic thrombocytopenic
purpura
Acute pancreatitis
Refractory
Plasmapheresis
author_facet Ebisa Bekele
Bethel Shiferaw
Alexandra Sokolova
Arpan Shah
Phillip Saunders
Alida Podrumar
Javed Iqbal
author_sort Ebisa Bekele
title Refractor y thrombotic thrombocytopenic pur pura following acute pancreatitis
title_short Refractor y thrombotic thrombocytopenic pur pura following acute pancreatitis
title_full Refractor y thrombotic thrombocytopenic pur pura following acute pancreatitis
title_fullStr Refractor y thrombotic thrombocytopenic pur pura following acute pancreatitis
title_full_unstemmed Refractor y thrombotic thrombocytopenic pur pura following acute pancreatitis
title_sort refractor y thrombotic thrombocytopenic pur pura following acute pancreatitis
publisher Wolters Kluwer Medknow Publications
series Journal of Acute Disease
issn 2221-6189
publishDate 2016-09-01
description Thrombotic thrombocytopenic purpura (TTP) is a rare blood disorder with an estimated incidence of 4–5 cases per million people per year. It is characterized by small-vessel platelet-rich thrombi that cause thrombocytopenia, microangiopathic hemolytic anemia and organ damage. There are reports in literature that TTP and acute pancreatitis are associated, indicating each can be the cause of the other. However, acute pancreatitis triggering TTP is very rare. A 71 years old female presented with abdominal pain of 3 days, followed by dark urine. She had icteric sclera, petechial rash and mild epigastric tenderness. Lab findings were significant for hemolytic anemia, thrombocytopenia and elevated lipase. CT of abdomen showed evidence of pancreatitis and cholelithiasis. After admission, patient developed symptoms of stroke. Further investigation showed elevated lactate dehydrogenase and normal coagulation studied with peripheral blood smear showed 5–6 schistocytes/high power field. Disintegrin and metalloproteinase with thrombospondin motifs-13 (ADAMTS13) activity showed less than 3% with high ADAMTS13 inhibitor 2.2. Patient required 6–7 weeks of daily plasmapheresis until she showed complete response. Our patient presented with clinical features of pancreatitis prior to having dark urine and petechial rash. Therefore, we strongly believe that our patient had pancreatitis which was followed by TTP. Patient's ADMTS13 activity was 6% after 10 plasma exchanges, signifying refractory TTP and higher risk for morbidity and mortality. There are limited data and consensus on the management of refractory TTP. TTP and acute pancreatitis are associated. However, refractory TTP following acute pancreatitis is rarely mentioned in the literature. We would like to emphasize the importance of having higher clinical suspicion of the association of both disease entities.
topic Thrombotic thrombocytopenic
purpura
Acute pancreatitis
Refractory
Plasmapheresis
url http://www.sciencedirect.com/science/article/pii/S2221618916301196
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AT arpanshah refractorythromboticthrombocytopenicpurpurafollowingacutepancreatitis
AT phillipsaunders refractorythromboticthrombocytopenicpurpurafollowingacutepancreatitis
AT alidapodrumar refractorythromboticthrombocytopenicpurpurafollowingacutepancreatitis
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