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...
Main Authors: | , , , , , , |
---|---|
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 |
id |
doaj-4dbc880e0f3f4911ae164f84e38d6aff |
---|---|
record_format |
Article |
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 |
work_keys_str_mv |
AT ebisabekele refractorythromboticthrombocytopenicpurpurafollowingacutepancreatitis AT bethelshiferaw refractorythromboticthrombocytopenicpurpurafollowingacutepancreatitis AT alexandrasokolova refractorythromboticthrombocytopenicpurpurafollowingacutepancreatitis AT arpanshah refractorythromboticthrombocytopenicpurpurafollowingacutepancreatitis AT phillipsaunders refractorythromboticthrombocytopenicpurpurafollowingacutepancreatitis AT alidapodrumar refractorythromboticthrombocytopenicpurpurafollowingacutepancreatitis AT javediqbal refractorythromboticthrombocytopenicpurpurafollowingacutepancreatitis |
_version_ |
1725382791320829952 |