scholarly journals A Rare Case of Coombs-Positive Hemolytic Anemia Due to Brown Recluse Spider Bite

Author(s):  
B. Ratakonda ◽  
C. Trabue
2016 ◽  
pp. bcr2016215832 ◽  
Author(s):  
Monique Cachia ◽  
Liam Mercieca ◽  
Charles Mallia Azzopardi ◽  
Michael J Boffa
Keyword(s):  

2015 ◽  
Vol 16 (2) ◽  
pp. 115-117
Author(s):  
Love Daoud ◽  
Vivian Shokry ◽  
Ehab Daoud

Gangrene is a rare and extreme presentation of cold agglutinin disease and our case is one of only few published reports in medical literature (less than twenty). In our patient severe hemolysis as manifested by elevated indirect bilirubin, LDH and low haptoglobin was triggered by unusual infectious organisms (E. Coli and Coagulase negative Staphylococcus).J MEDICINE July 2015; 16 (2) : 115-117


1994 ◽  
Vol 32 (4) ◽  
pp. 451-456 ◽  
Author(s):  
Lindsay M. Murray ◽  
Donna L Seger
Keyword(s):  

2021 ◽  
Vol 51 (2) ◽  
Author(s):  
Emin Gemcioglu ◽  
Mehmet Kayaalp ◽  
Merve Caglayan ◽  
Ahmet Ceylan ◽  
Mehmet Sezgin Pepeler

Thrombotic Thrombocytopenic Purpura is a syndrome of microangiopathic hemolytic anemia accompanied by thrombocytopenia, neurological disorders, renal failure and fever. Acute pancreatitis is a rare cause of Thrombotic Thrombocytopenic Purpura and this manifestation, at the same time, is a rare complication of acute pancreatitis. Thrombotic Thrombocytopenic Purpura is induced in acute pancreatitis by poorly understood mechanism, which involves multiple pathways apart from only ADAMTS-13 deficiency. Here, we analyze the case of a 47-year-old female who presented with an acute pancreatitis. She was diagnosed with Thrombotic Thrombocytopenic Purpura and an acute pancreatitis at the same time, with thrombocytopenia and peripheral smear findings at presentation. Therefore, Thrombotic Thrombocytopenic Purpura secondary to the pancreatitis was considered in this case. In this work, we have discussed details of our case and the different mechanisms involved in pathogenesis of Thrombotic Thrombocytopenic Purpura in acute pancreatitis and their outcome with prompt management.


2021 ◽  
pp. 26-27
Author(s):  
Tony K S ◽  
Rakhee joshi ◽  
Alok Parekh ◽  
Saurabh Atey ◽  
Payal Tayade

Infectious mononucleosis (IM) is often an uncomplicated self-limited illness resulting from Epstein-Barr virus (EBV) in 90% cases. This is a case report of 21-year-old female whose initial clinical and laboratory presentation suggested Heterophile antibody negative Epstein–Barr Viral capsid Antigen (VCA) IgM positive infectious Mononucleosis. Our case was complicated by biliary stasis, cold autoimmune hemolytic anemia with acrocyanosis, thrombocytopenia and some of the features of hemophagocytic lymphohistiocytosis (HLH). Following symptomatic management patient recovered. Physicians should routinely counsel their patients with IM for these complications and should avoid overzealous treatment


2021 ◽  
pp. 1-3
Author(s):  
Christina Hadjiaggelidou ◽  
George Douganiotis ◽  
Kyriaki Tsirou ◽  
Evgenia Verrou ◽  
Theodora Triantafyllou ◽  
...  

Author(s):  
Durga Krishnan ◽  
Kaliyannan Mayilananthi ◽  
Vrinda Vijayakumari ◽  
Thejesh Chikmangalur Vishwanath

Tuberculosis is one of the oldest diseases known to mankind. The disease still puzzles us with its varied clinical presentations and complications. Though tuberculosis is known to have many hematological manifestations, auto immune hemolytic anemia is extremely rare in tuberculosis. Here we report aninteresting case of tuberculosis presenting with auto immune hemolytic anemia. The treatment withanti tuberculous therapy is enough for the managing tuberculosis associated auto immune hemolyticanemia.


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