Lymphoid Malignancy in Common Variable Immunodeficiency in a Single Center Cohort

Author(s):  
Tukisa Smith ◽  
Charlotte Cunningham‐Rundles
2020 ◽  
Vol 18 (1) ◽  
pp. 30-37
Author(s):  
Gökhan AYTEKİN ◽  
Eray YILDIZ ◽  
Fatih ÇÖLKESEN ◽  
Şevket ARSLAN ◽  
Ahmet Zafer ÇALIŞKANER

2014 ◽  
Vol 27 (3) ◽  
pp. 533
Author(s):  
Raed Alzyoud ◽  
Zeyad Habahbeh ◽  
Mohammad Mutereen ◽  
Adel Wahadneh ◽  
Mohammad Abu-Shukair

2016 ◽  
Vol 176 ◽  
pp. 97-104 ◽  
Author(s):  
Dijana Perovic ◽  
Vladimir Perovic ◽  
Vera Pravica ◽  
Branka Bonaci-Nikolic ◽  
Radovan Mijanovic ◽  
...  

2020 ◽  
Vol 40 (3) ◽  
pp. 494-502
Author(s):  
Ismail Yaz ◽  
Begum Ozbek ◽  
Yuk Yin Ng ◽  
Pinar Gur Cetinkaya ◽  
Sevil Oskay Halacli ◽  
...  

2017 ◽  
Vol 47 ◽  
pp. 1-12 ◽  
Author(s):  
Uğur Haci MUŞABAK ◽  
Fevzi Sait DEMİREL YEŞİLLİK ◽  
Abdullah BAYSAN ◽  
Ali SELÇUK ◽  
Özgür KARTAL ◽  
...  

Blood ◽  
2008 ◽  
Vol 112 (2) ◽  
pp. 277-286 ◽  
Author(s):  
Helen Chapel ◽  
Mary Lucas ◽  
Martin Lee ◽  
Janne Bjorkander ◽  
David Webster ◽  
...  

AbstractThe European Common Variable Immunodeficiency Disorders registry was started in 1996 to define distinct clinical phenotypes and determine overlap within individual patients. A total of 7 centers contributed patient data, resulting in the largest cohort yet reported. Patients (334), validated for the diagnosis, were followed for an average of 25.6 years (9461 patient-years). Data were used to define 5 distinct clinical phenotypes: no complications, autoimmunity, polyclonal lymphocytic infiltration, enteropathy, and lymphoid malignancy. A total of 83% of patients had only one of these phenotypes. Analysis of mortality showed a considerable reduction in the last 15 years and that different phenotypes were associated with different survival times. Types of complications and clinical phenotypes varied significantly between countries, indicating the need for large, international registries. Ages at onset of symptoms and diagnosis were shown to have a Gaussian distribution, but were not useful predictors of phenotype. The only clinical predictor was polyclonal lymphocytic infiltration, which was associated with a 5-fold increased risk of lymphoid malignancy. There was widespread variation in the levels of serum immunoglobulin isotypes as well as in the percentages and absolute numbers of B cells, confirming the heterogeneity of these conditions. Higher serum IgM and lower circulating CD8 proportions were found to be predictive markers for polyclonal lymphocytic infiltration and autoimmunity, respectively.


Praxis ◽  
2007 ◽  
Vol 96 (1) ◽  
pp. 3-11
Author(s):  
Suter-Meyer ◽  
Nigg ◽  
Kolyvanos Naumann ◽  
Käser ◽  
Vetter

2015 ◽  
Author(s):  
Ishrat Khan ◽  
Mirena Noyvirt ◽  
Aicha Bouraoui ◽  
Penny Owen ◽  
Helen Lane

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