Table 2

Comparison between sarcoidosis and Wegener granulomatosis

SarcoidosisWegener granulomatosis
Clinical presentation
Upper airwayOccurs in <10% of casesExtremely common
LungCommon
Adenopathy
Diffuse infiltrates, usually upper lobes
Common
Nodular infiltrates, sometimes with cavities
Infiltrates localised to areas of haemorrhage, often lower lobe
EyeUveitis, retinitis, optic neuritisEpiscleritis
SkinMaculopapular lesionsVasculitic lesions
Lupus pernioOccasionally seen
KidneyGlomerulopnephritis rare, renal failure usually due to hypercalcaemiaFocal necrotising glomerulitis in over half of cases
Neurological disease10% of patients. Often mass seen on MRIUp to 30% of cases will have lesions. Usually due to vasculitic lesions
JointsUncommon. Can see specific bone cystsUncommon
Tracheal/proximal airway stenosisRareCommon
ANCANegativePositive in >80% of cases
ACEPositive in >60% of new casesNegative
Treatment
CorticosteroidsDrug of choice for initial managementSupportive but not used for maintenance therapy
MethotrexateEffectiveEffective
AzathioprineEffectiveEffective
CyclophosphamideReserved for refractory casesTreatment for extensive disease
Anti-TNF therapyEffective for refractory diseaseNot effective for most patients
RitixumabEffectiveness unknownEffective for refractory cases
  • ANCA, antineutrophil cytoplasmic antibody; TNF, tumour necrosis factor.