Table 1.
Low-risk sarcoidosis | Intermediate-risk sarcoidosis | High-risk sarcoidosis • Factors warranting intensive treatment |
Lofgrens syndrome | ||
Nodal sarcoidosis | ||
Scar sarcoidosis | ||
(Ankle) arthritis | Osseous sarcoidosis | |
Uncomplicated or local cutaneous involvement | Lupus Pernio (known to warrant long-term treatment) | |
Uncomplicated uveitis | Chronic or severe uveitis • Loss of vision | |
Mild hypercalcemia hypercalciuria with nefrocalcinosis | Severe hypercalcemia (known to warrant long-term treatment) | |
Possible cardiac sarcoidosis | Probable or definite cardiac sarcoidosis • Large extent of involvement on CMR or FDG-PET • Rhythm or function abnormalities | |
Parenchymal sarcoidosis without impaired PFT | Progressive fibrosing pulmonary sarcoidosis • Impaired pulmonary function • High inflammatory burden and signs of fibrosis on FDG-PET/CT | |
Central nervous system sarcoidosis • Spinal cord involvement • Hydrocephalus | ||
Hepatic sarcoidosis |
Simplified stratification of sarcoidosis examples into risk categories. Risk of organ damage or mortality are taken into account. Low-risk sarcoidosis can be managed by watchful waiting and screening for organ involvement. Intermediate-risk sarcoidosis should be managed case-by-case, some patients warrant systemic treatment following current guidelines with a step-up regime. High-risk sarcoidosis warrants systemic treatment and could potentially benefit from a more aggressive ‘top-down’ or ‘hit-hard’ regimen with a more upfront use of steroid sparing agents or in some cases even biologicals. CMR Cardiac Magnetic Resonance Imaging; FDG, fluorodeoxyglucose; PFT, pulmonary function test.