Steroid-Responsive Idiopathic Cold Agglutinin Disease: A Case Report

1989 ◽  
Vol 81 (3) ◽  
pp. 166-168 ◽  
Author(s):  
M. Lahav ◽  
I. Rosenberg ◽  
A.J. Wysenbeek
2021 ◽  
Vol 14 (5) ◽  
pp. e241294
Author(s):  
Yisi D Ji ◽  
Paul M Cavallaro ◽  
Britlyn D Orgill

An 80-year-old man with idiopathic cold agglutinin disease presented with acute cholecystitis. We describe operating room and anaesthetic considerations for patients with cold agglutinin disease and measures that can be taken to prevent disease exacerbation in this case report. Multidisciplinary collaboration and planning between the operative room staff, anaesthesia team and surgical team are needed to ensure safe surgery and optimal patient outcomes.


2019 ◽  
Vol 85 ◽  
pp. S68-S69
Author(s):  
S. Çelik ◽  
Z. Güven ◽  
B. Eser ◽  
L. Kaynar ◽  
M. Çetin ◽  
...  

2020 ◽  
Vol 27 (5) ◽  
pp. 411-412
Author(s):  
Haruna Yamamoto ◽  
Satoru Kayama ◽  
Taichi Onimaru ◽  
Midori Imaizumi ◽  
Kinuko Kubota ◽  
...  

2003 ◽  
Vol 45 (1) ◽  
pp. 157
Author(s):  
Francis Sahngun Nahm ◽  
Jong Sung Kim ◽  
Byung Moon Ham ◽  
Hyun Soo Moon ◽  
Sung Hee Han

2020 ◽  
Vol 154 (Supplement_1) ◽  
pp. S165-S165
Author(s):  
M M Yilmaz ◽  
Y Tanhehco

Abstract Introduction/Objective Autoimmune hemolytic anemia (AIHA) is a group of disorders with limited epidemiological and clinical data, characterized by hemolysis due to autoantibodies against red blood cell surface antigens. Cold agglutinins account for about 25% of all AIHA, which can agglutinate erythrocytes at 0-4 °C. Cold agglutinin disease (CAD) is a self limited disease and usually does not cause significant hemolysis. Here, we report a case with an unusually severe course for secondary CAD and role of plasma exchange in the management. Methods A 53-year-old male patient with no known past medical history presented to the emergency department with shortness of breath and syncope after a week of upper respiratory tract infection symptoms. The patient became profoundly anemic (presented with 8.1 g/dL hemoglobin level and progressively decline to 4.2 g/dL) in a short period of time. Upon initial evaluation, his peripheral blood smear demonstrated clumps of RBCs. Direct anti-globulin testing was negative for IgG but positive for C3 which is consistent with CAD. A respiratory PCR panel detected Rhinovirus. Mycoplasma and EBV IgM were negative. Additionally, chest X-ray showed right middle lobe pneumonia that was treated with antibiotics. Patient received multiple transfusions of pre-warmed pRBCS and showed initial improvement but eventually went into respiratory failure and cardiac arrest with return of spontaneous circulation after 8 minutes of CPR. Subsequently, plasma exchange was started. Only after intiation of plasma exchange, the patient’s ongoing hemolysis was stabilized. Conclusion This case report presents a patient with unexpectedly rapid and severe hemolysis from secondary cold agglutinin disease. Interestingly, the case appeared not to be caused by EBV or Mycoplasma pneumonia infection but Rhinovirus. Further studies confirmed patient had no autoimmune disorder or lymphoid malignancy that may had initiated secondary CAD. On the management aspect, pre-warmed RBC transfusions were not sufficient to stabilize the patient’s condition. Plasma exchange was able to control ongoing hemolysis within 2 sessions successfully.


2018 ◽  
Vol 12 (1) ◽  
Author(s):  
Thomas A. Vo ◽  
Zack Oakey ◽  
Yasir A. Khan ◽  
Donald S. Minckler

2021 ◽  
Vol 24 ◽  
pp. S207
Author(s):  
F. Joly ◽  
L.A. Schmitt ◽  
P.A. McGee Watson ◽  
E. Pain ◽  
D. Testa

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