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Table 1 Clinical and genetic characteristics of patients with XHIGM with PAP with the CD40LG mutation

From: CD40LG-associated X-linked Hyper-IgM Syndrome (XHIGM) with pulmonary alveolar proteinosis: a case report

Patient no.

Present patient

Patient 2(6)

Patient 3(7)

Patient 4(8)

 

Age of onset (months)

5

5

12

9

 

Age at diagnosis (months)

7

5

60

36

 

Delay in diagnosis (months)

2

0

48

25

 

Predominant infections

Pneumonia

Pneumonia

Pneumonia/diarrhea

Pneumonia

 

Organisms isolated

Fungi

No

Klebsiella pneumoniae

Pneumocystis jirovecii

 

Other manifestations

NA

No

Recurrent anemia

No

 

IgG (mg/dl)

81 (800–1600)

< 80 (139–655)

308 (490-1 610)

40 (100–560)

 

IgA (mg/dl)

< 7 (70–330)

8 (4–62)

65 (40–200)

150 (360–920)

 

IgM (mg/dl)

57 (50–220)

108 (17–69)

314 (50–200)

480 (400–1280)

 

Neutropenia

Yes

NA

No

Yes

 

Chest CT

Ground-glass density images in both lungs

Diffuse ground glass opacities, reticular interstitial thickening, and consolidation

Ground-glass density images in both lungs

Ground-glass density images in both lungs

 

Pathology

BAL material PAS (+)

BAL material PAS (+)

Lung biopsy revealed PAS (+)

BAL material PAS (+)

 

Mutations/domains

c.516T > A, p.Tyr172Ter/TNFH

c.608G > C, p.Arg203Thr/TNFH

IVS3-1 G > A, E4 skip (del 347–409)/TNFH

c.511 dup A, p. Ile171Asn30/TNFH

 

Treatment given and outcomes

Recovery on WLL, IVIg, cotrimoxazole, and HSCT

Improved on steroids, IVIg and WLL

Improved on IVIg, cotrimoxazole,

Improved on WLL, methylprednisolone, IVIg

 

Follow-up (months)

42

12

96

36

  1. Abbreviations: BAL, bronchoalveolar lavage; HSCT, hematopoietic stem cell transplantation; IVIg, intravenous immunoglobulin; NA, not available; PAS, periodic acid-Schiff; TNFH, tumor necrosis factor homology domain; WLL, whole-lung lavage