Sarcoidosis: Current Understanding of Diagnosis and Management

Understanding Sarcoidosis: Current Perspectives

Sarcoidosis is characterised by the presence of non-caseating granulomas in affected organs, most commonly the lungs and lymph nodes, but also the skin, eyes, liver, heart, and nervous system.¹ The aetiology remains unknown, though genetic predisposition and environmental triggers are implicated.² Diagnosis requires a compatible clinical and radiological presentation, histological evidence of non-caseating granulomas, and the exclusion of other granulomatous diseases, such as tuberculosis, fungal infections, or berylliosis.^1,3

Pulmonary sarcoidosis is the most frequent manifestation, affecting over 90% of patients.⁴ Chest radiography and high-resolution computed tomography (HRCT) are crucial for staging and monitoring lung involvement. The Löfgren syndrome, characterised by acute arthritis, erythema nodosum, and bilateral hilar lymphadenopathy, is a self-limiting form of sarcoidosis with a favourable prognosis, often not requiring systemic treatment.⁵ In contrast, chronic or progressive pulmonary sarcoidosis can lead to irreversible fibrosis and significant morbidity.⁴

Diagnostic Approaches and Management Strategies

Biopsy of an affected organ is often necessary to confirm the diagnosis. Bronchoscopy with transbronchial lung biopsy (TBLB) or endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA) are common procedures for pulmonary involvement, yielding diagnostic rates of 50-90% and 80-90% respectively.⁶ Serum angiotensin-converting enzyme (ACE) levels can be elevated in sarcoidosis, but their sensitivity and specificity are insufficient for diagnostic purposes alone; they are more useful for monitoring disease activity in some patients.⁷

Treatment decisions are guided by the severity of symptoms, the extent of organ involvement, and the risk of irreversible organ damage. Asymptomatic patients with stable disease, particularly those with Löfgren syndrome, may only require observation.⁵ Systemic corticosteroids, such as prednisone, are the cornerstone of treatment for symptomatic or progressive sarcoidosis, typically initiated at doses of 20-40 mg/day for several weeks, followed by a slow taper.⁸ The duration of treatment varies but often extends for 6-12 months or longer.⁸

For patients who are intolerant to corticosteroids, require high doses for prolonged periods, or have refractory disease, steroid-sparing immunosuppressants are employed. Methotrexate, at doses of 10-15 mg/week, and azathioprine, at 1-2 mg/kg/day, are commonly used second-line agents.⁹ These agents may take several months to achieve their full therapeutic effect.⁹ Hydroxychloroquine can be effective for cutaneous sarcoidosis and hypercalcaemia.¹⁰ Tumour necrosis factor-alpha (TNF-α) inhibitors, such as infliximab or adalimumab, are reserved for severe, refractory sarcoidosis, particularly in cases of neurosarcoidosis or cardiac sarcoidosis, where other treatments have failed.¹¹

Cardiac sarcoidosis, though less common, carries a significant risk of sudden cardiac death due to arrhythmias and heart failure. Early diagnosis via cardiac magnetic resonance imaging (CMR) and positron emission tomography (PET) scanning is critical, and treatment often involves corticosteroids and immunosuppressants, alongside antiarrhythmic agents or implantable cardioverter-defibrillators (ICDs).¹² Neurosarcoidosis also requires aggressive treatment due to the potential for severe neurological deficits.¹³

Limitations in current understanding include the lack of reliable biomarkers for predicting disease progression or treatment response, and the absence of curative therapies. Research continues into novel therapeutic targets and personalised medicine approaches.¹⁴