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Table 3 The demograghic data, immunological and genetic findings of 8 patients with caspase-8 deficiency

From: A rare immunological disease, caspase 8 deficiency: case report and literature review

Subject

Patient 1a [19]

Patient 2a [19]

 

Patient 3b [20]

Patient

4b[20]

Patient

5 [21]

Patient

6 [21]

Patient

7 [21]

Patient 8

Age of onset

(Year)

12y

11y

 

38y

37y

Whitin the first years of life

Within the first years of life

Within the first years of life

2y

Gender

Female

Male

 

Female

Male

NA

NA

NA

Male

First presentation

LAP and splenomegaly

LAP and splenomegaly

 

Acute shortness of breath

Complex neurological syndrome

Recurrent fever

Bloody diarrhea, recurrent infections and fever

Non-bloody diarrhea, recurrent infections

FUO, dysentery

Symptoms

Poor response to immunization, organomegaly, sinopulmonary and herpes simplex virus infection

Poor response to immunization, organomegaly, sinopulmonary and herpes simplex virus infection

 

Pneumonia,

Pulmonary hypertension,

Interstitial lung disease, high grade fever, pancytopenia,

multiple necrotizing and non-necrotizing granulomas of lung

1 cm3 mass at the Meckel’s cave(necrotizing granuloma)

aspiration pneumonia, bronchiectasis,

organomegaly

Multinodular lesions in liver and spleen, cranial nerve palsy/paresis

FTT, diarrhea, perianal disease, proctocolitis, refractory colitis increased susceptibility to bacterial and viral infections, multiple food allergy with mild peripheral eosinophilia and chronic eosinophilic infiltration antrum and duodenum Chronic eczema, pityriasis amiantacea, and hypothyroidism

FTT, diarrhea, perianal disease, proctocolitis, increased susceptibility to bacterial and viral infections,

Refractory colitis

FTT, perianal disease, proctocolitis. increased susceptibility to bacterial and viral infections, intestinal obstruction,

Refractory

colitis

FUO, dysentry, FTT, lymphadenopathy, allergy to cow's milk protein, splenomegaly, Perianal fissures, Crohn's disease

Failure to thrive

+

+

 

+

+

+

+

Lymphadenopathy

+

+

 

+

Splenomegaly

+

+

 

+

+

+

Eczema

+

+

 

+

Reactive airway disease

+

+

 

Pneumonia

+

+

 

+

+

+

Not mentioned

+

HSV labialis

+

+

 

Chronic diarrhea

+

 

+

+

+

+

Food allergy

 

+

+ (bovine protein allergy)

Infections

sinopulmonary and herpes simplex virus infection

sinopulmonary and herpes simplex virus infection

 

Acute EBV infection, Nocardia asteroids meningoencephalitis, pneumonia

Aspiration pneumonia

Pneumonia, otitis media, conjuctivitis, purulent dermatitis, molluscum contagiosum, and local infections

   

Cause of death

   

Nocardia asteroids meningoencephalitis

Progressive neurological and pulmonary complications

Alive

Septic complications

Alive

Alive

Genetic test

homozygous CASP 8 mutation

c.919C > T; p.R307W

homozygous CASP 8 mutation

c.919C > T; p.R307W

 

homozygous CASP 8 mutation

c.919C > T; p.R307W

homozygous CASP 8 mutation

c.919C > T; p.R307W

homozygous CASP8 mutation

c.836A>G, p.Q279R

homozygous CASP8 mutation

c.836A > G, p.Q279R

homozygous CASP 8 mutation

c.919C > T; p.R307W

homozygous CASP8 mutation

c.1572G > T

p.Q524H

Immunoglobulin concentration

IgG: normal

IgA: normal

IgM: normal

IgE:

normal

IgG: low

IgA: normal

IgM: low

IgE:normal

 

IgG:

normal

IgA:

normal

IgM:

Low

IgE:

normal

IgG:

normal

IgA:

normal

IgM:

Low

IgE:

normal

Not available

Not available

Not available

IgG: normal

IgA: low

IgM: normal

Total lymphocytes

1510

(normal)

2362

(normal)

 

990

(low)

3710

(high)

Not available

Not available

Not available

5487

(high)

CD4%

23.1

(low)

25

(low)

 

23.5

(low)

9.3

(low)

Not available

Not available

Not available

10

CD8%

49.6

(normal)

46.2

(normal)

 

65.6

(normal)

87.6

(high)

Not available

Not available

Not available

22

CD4/CD8 ratio

0.5

(low)

0.5

(low)

 

0.35

(low)

0.1

(low)

Not available

Not available

Not available

0.45

(normal)

B Lymphocytes

361

570

 

Not available

Not available

Not available

Not available

Not available

Not available

  1. (Patient number 8 is the case presented in this study)
  2. FTT failure to thrive, LAP lymphadenopathy, FUO fever of unknown origin, NA Not Available
  3. aPatient number 1 and 2 were siblings
  4. bPatients number 3 and 4 were siblings