Sarcoidosis
Sarcoidosis is a multi-system, non-caseating granulomatous inflammatory condition. Granulomas are nodules of inflammation, and are full of macrophages. There are 2 types of granulomas:
Caseating (necrotic centre) – Associated with infection
Non-caseating (no necrotic centre) – Associated with inflammation
A typical patient here is a 20-40 year old black women presenting with a dry cough and SOB, and may have erythema nodosum.
Patients usually present with pulmonary symptoms, and multiple extra-pulmonary manifestations, such as erythema nodosum and lymphadenopathy.
Lofgren’s Syndrome - Acute Sarcoidosis - Presents with a triad of bilateral hilar lymphadenopathy, polyarthralgia, and erythema nodosum.
Affected Organs
Lungs (>90%) – Mediastinal lymphadenopathy, Pulmonary fibrosis, Granulomas
Liver – Granulomas, Cirrhosis, Cholestasis
Eyes – Uveitis, Conjunctivitis, Optic neuritis
Skin – Erythema nodosum, Lupus pernio (raised, purple lesions on cheeks and nose), Granulomas on scar tissue
Heart – BBB, Heart block, Myocardial muscle involvement
Kidneys – Stones, Nephrocalcinosis (calcium deposition), Interstitial nephritis
Investigations
Diagnosed with a tissue biopsy, which will show non-caseating granulomas.
Investigations to do include:
Bloods - Raised ESR, Raised ACE, Hypercalcaemia
Imaging - CXR, CT Chest, PET (shows active inflammation in affected areas)
Management
No treatment required if bilateral hilar lymphadenopathy alone as it usually resolves spontaneously within 6 months for most patients.
Acute Sarcoidosis:
1st line - Rest, NSAIDs, Steroids (for 6-24 months)
Patients should be co-prescribed bisphosphonates for bone protection
2nd line - Immunosuppressants e.g. Methotrexate or Azathioprine

