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Table 4 Type of PHID and PHID complications in 5 clusters of 79 PHID patients, ALTADIH Cohort, 2007-2010

From: T-cell activation discriminates subclasses of symptomatic primary humoral immunodeficiency diseases in adults

 

Cluster 1

Cluster 2

Cluster 3

Cluster 4

Cluster 5

n = 33

n = 18

n = 4

n = 8

n = 16

 

n

%

n

%

n

%

n

%

n

%

Type of PHID

          

     CVID

23

(70)

8

(44)

3

(75)

8

(100)

13

(82)

     IgG subclass deficiency

10

(30)

10

(56)

0

(0)

0

(0)

1

(6)

     Good’s syndrome

0

(0)

0

(0)

1

(25)

0

(0)

2

(12)

PHID complications (at least one of the following)

5

(15)

6

(33)

3

(75)

7

(88)

10

(63)

     Lymphoid hyperplasia

2

(6)

5

(28)

1

(25)

3

(38)

5

(31)

     Splenomegaly

1

(3)

2

(11)

1

(25)

7

(88)

3

(19)

     Autoimmune manifestations

3

(9)

1

(5)

1

(25)

2

(25)

7

(44)

     Granulomatous disease

0

(0)

1

(5)

2

(50)

4

(50)

2

(13)

     Villous atrophy

0

(0)

2

(11)

0

(0)

0

(0)

3

(19)

     Chronic inflammatory intestinal disease

0

(0)

2

(11)

1

(25)

1

(13)

0

(0)