Table 1– Patient characteristics at the time of diagnosis of interstitial lung disease in combined variable immunodeficiency disorder associated with granulomatous disease (GD)
PatientSex/ethnicityRecurrent infectionsAutoimmune disorderRespiratory symptomsAuscultationExtrathoracic involvement of GD
1M/cNNDCracklesSkin
2M/cNNNCracklesLiver, spleen
3M/bNNNnSpleen, pLN, aLN
4F/cYNDNDSpleen, aLN
5M/cYNNnLiver, spleen, aLN, BM
6F/cNThrombocytopenia, anaemiaNnSpleen, aLN
7F/cYNNnSkin, pLN
8M/cYND, CnLiver, spleen, eyes, PFNP
9M/cNNDCracklesLiver, spleen
10F/cYBiermer’s anaemia, Hashimoto’s thyroiditisD, CCracklesLiver, spleen, pLN, aLN, parotitis
11F/cYSicca syndromeDCracklesSpleen
12F/cYThrombocytopeniaD, CCracklesLiver, spleen
13M/cYNeutropeniaD, CCracklesLiver, spleen
14M/cYNNnSpleen, eyes, parotitis, CNS
15M/cYLupusNNDLiver, spleen, aLN
16M/bYNNnSpleen, pLN
17M/cYAnaemia, neutropeniaDCracklesNone
18F/cYND, CCracklesSpleen, skin, aLN
19F/cNThrombocytopeniaDnLiver, spleen, eyes, CNS
20F/cNNNnSpleen
  • M: male; F: female; c: Caucasian; b: black; N: no; Y: yes; D; dyspnoea; C: cough; n: normal; ND: not determined; p: peripheral; LN: lymph node; a: abdominal; BM: bone marrow; PFNP: peripheral facial nerve paralysis; CNS: central nervous system.