Common Variable Immunodeficiency Causing Non-cirrhotic Portal Hypertension: Case Report and a Review of Literature

2013 ◽  
Vol 108 ◽  
pp. S349-S350
Author(s):  
Jean Ong Kian Koc ◽  
Victor Navarro ◽  
Ronald Miick
Keyword(s):  
Case Report ◽  
Portal Hypertension ◽  
Common Variable Immunodeficiency ◽  
Review Of Literature ◽  
Common Variable

CHARGE syndrome and common variable immunodeficiency: A case report and review of literature

2016 ◽  
Vol 27 (5) ◽  
pp. 546-550 ◽  
Author(s):  
Baldassarre Martire ◽  
Raffaella Panza ◽  
Marta Pillon ◽  
Maurizio Delvecchio
Keyword(s):  
Case Report ◽  
Common Variable Immunodeficiency ◽  
Charge Syndrome ◽  
Review Of Literature ◽  
Common Variable

Resolution of Hypersplenism and Pancytopenia in Common Variable Immunodeficiency Patient After Partial Splenic Artery Embolization: A Case Report and Review of Literature

2015 ◽  
Vol 4 (2) ◽  
pp. 174-177
Author(s):  
Safiah Hussain Sumayli ◽  
Latifah Rashed Al Shekaili ◽  
Sulaiman Saleh Al Gazlan ◽  
Farrukh Sheikh ◽  
Hassan Al Rayes ◽  
...  
Keyword(s):  
Case Report ◽  
Common Variable Immunodeficiency ◽  
Splenic Artery ◽  
Review Of Literature ◽  
Artery Embolization ◽  
Splenic Artery Embolization ◽  
Common Variable

scholarly journals COMMON VARIABLE IMMUNODEFICIENCY MIMETIZING CASE OF SPONDILOARTROPATHY – CASE REPORT

2019 ◽  
Author(s):  
DIOGO CUNHA LACERDA ◽  
RODRIGO ZUBER MACIEL ◽  
LUCAS ANDROCZEVECZ SILVA ◽  
JEAN TAFAREL BOBATO ◽  
RAFAELA SORPILE ARAUJO ◽  
...  
Keyword(s):  
Case Report ◽  
Common Variable Immunodeficiency ◽  
Common Variable

scholarly journals Common variable immunodeficiency – case report

2013 ◽  
Vol 3 (2) ◽  
pp. 170-172
Author(s):  
Emina Vukas ◽  
Aida Dizdarević ◽  
Senka Mesihović - Dinarević ◽  
Adisa Čengić
Keyword(s):  
T Cells ◽  
Dendritic Cells ◽  
Case Report ◽  
Immune System ◽  
Primary Immunodeficiency ◽  
Common Variable Immunodeficiency ◽  
Clinical Picture ◽  
Clinical Signs ◽  
Common Variable

Common variable immunodeficiency (CVID) or acquired hypogammaglobulinemia is the type of primary immunodeficiency. Deregulation of the immune system, leading to hypogammaglobulinemia, defective activation and proliferation of T cells and dendritic cells, and malfunction of the cytokines are observed in CVID. The clinical picture of CVID varies, any organ or system can be affected, therefore the diagnosis is often difficult and delayed and sometimes is not always possible. This article describes a twelve years old boy with all the clinical signs of immunodeficiency, as confi rmed by laboratory. The main treatment consists of life-long immunoglobulin substitution in intravenous or subcutaneous form.

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