Author's details
- Dr Bashir Taiye Aminu.
- MBBS (Ilorin) FWACP (Int. Med./Pulmunology) MHE (BUK) Cert LMIH and FGHR (Washington) IR (Malaysia/UNU) ECFMG-EPIC Certified Physician
Reviewer's details
- Dr Jafaru Momodu
- MBBS, ACP Member, Member NPGMCN, FWACP Pulmonology.
- National Hospital Abuja. Researcher.
- Date Uploaded: 2026-03-11
- Date Updated: 2026-03-11
Sarcoidosis
Key Messages
- Sarcoidosis is a multisystem granulomatous disease of unknown cause, often mimicking tuberculosis in Africa.
- It commonly presents pulmonary symptoms like dry cough and dyspnea, alongside systemic and extrapulmonary features.
- Diagnosis relies on biopsy showing non-caseating granulomas and careful exclusion of tuberculosis.
- Treatment ranges from observation in mild cases to corticosteroids and immunosuppressants in progressive disease.
- Underdiagnosis is common in Africa due to TB similarities, making early specialist referral critical.
Multisystem granulomatous disorder of unknown aetiology, characterized by non-caseating granulomas. Genetic predisposition with environmental triggers postulated. African Americans have more severe, extrapulmonary disease. African data is limited but suggests different clinical patterns.
African Context: Underreported in Nigeria; most cases diagnosed incidentally. Possibly misdiagnosed as tuberculosis due to clinical and radiological similarities. (Igbokwe et al., 2020; Nigerian Postgraduate Medical Journal)
Symptoms & Clinical Features
- Pulmonary: Dry cough, dyspnea, chest discomfort (50-80%)
- Systemic: Fatigue, fever, weight loss
- Extrapulmonary: Skin lesions (erythema nodosum, lupus pernio), ocular (uveitis), lymphadenopathy, Neurosarcoid, cardiac sarcoid, hepatic involvement.
- Scadding stages: 0-4 based on CXR appearance
- African presentation: Higher rates of cutaneous and severe pulmonary involvement (Benjelloun et al., 2013; African Health Sciences)
Differential Diagnosis
- Tuberculosis (major differential in endemic regions)
- Fungal infections (histoplasmosis)
- Lymphoma: presenting with bi-halar lymphadenopathy
- Hypersensitivity pneumonitis: with widespread infiltrate on chest radiograph. History of exposure to antigens
- Berylliosis
Investigations
- Histology: Non-caseating granulomas on biopsy (transbronchial, skin, lymph node)
- Radiology: Bilateral hilar lymphadenopathy (BHL), parenchymal infiltrates
- Laboratory: Elevated ACE (nonspecific), hypercalcemia, abnormal LFTs
- PFTs: Restrictive pattern with reduced DLCO
Diagnostic challenge in TB-endemic areas: Need to exclude TB with cultures/PCR before immunosuppression (Okwor et al., 2021)
Treatment
- Asymptomatic Stage I: Observation (60-80% resolve spontaneously)
- Symptomatic/progressive: Corticosteroids (prednisone 20-40mg daily)
- Steroid-sparing: Methotrexate, azathioprine, anti-TNF for refractory cases
- African consideration: Always rule out TB before immunosuppression; monitor for opportunistic infections and prevent reactivation of latent ones.
Follow-up
- 3-6 monthly for active disease, Monitor symptoms, CXR, PFTs, extrapulmonary manifestations
- Screen for complications (pulmonary fibrosis, cardiac, neurosarcoidosis)
Prevention & Control
No known prevention: early diagnosis prevents organ damage through timely treatment
Conclusion and Experience from the clinic
Sarcoidosis in Nigeria is likely underdiagnosed due to TB mimicry. Increased awareness and access to biopsy/histopathology are needed for accurate diagnosis and appropriate management.
In practice, a few numbers of sarcoid patients have been diagnosed with the highest index of suspicion. Chronic cough with non-specific symptoms makes PTB to be the first consideration, others with endobronchial granuloma presenting with wheezing also brought asthma/hyper-reactive airway syndrome into though among others. Flexible bronchoscopy with endobronchial/transbronchial biopsy with BAL and histology with other ancillary investigations have mostly been the illuminating end of the tunnel. Hence, not all that wheeze is asthma, and TB is not the only cause of chronic cough. Early referral to the specialist could prevent life-threatening complications.
A 45-year-old non-smoking woman presents with a 3-month history of dry cough, fatigue, and unintentional weight loss. Chest X-ray reveals bilateral hilar lymphadenopathy, and TB tests are negative. Bronchoscopy with transbronchial biopsy shows non-caseating granulomas. She is diagnosed with pulmonary sarcoidosis and started on oral corticosteroids due to progressive symptoms.
Related Topics
- Igbokwe EU, et al. (2020). Sarcoidosis in Nigeria: A case series and review of challenges. Nigerian Postgraduate Medical Journal.
- Benjelloun H, et al. (2013). Sarcoidosis in Morocco: review of 120 cases. African Health Sciences.
- Baughman RP, et al. (2021). Sarcoidosis diagnosis and treatment: ATS/ERS/WASOG statement.
More topics to explore
Author's details
Reviewer's details
Sarcoidosis
- Background
- Symptoms
- Clinical findings
- Differential diagnosis
- Investigations
- Treatment
- Follow-up
- Prevention and control
- Further readings
Multisystem granulomatous disorder of unknown aetiology, characterized by non-caseating granulomas. Genetic predisposition with environmental triggers postulated. African Americans have more severe, extrapulmonary disease. African data is limited but suggests different clinical patterns.
African Context: Underreported in Nigeria; most cases diagnosed incidentally. Possibly misdiagnosed as tuberculosis due to clinical and radiological similarities. (Igbokwe et al., 2020; Nigerian Postgraduate Medical Journal)
- Igbokwe EU, et al. (2020). Sarcoidosis in Nigeria: A case series and review of challenges. Nigerian Postgraduate Medical Journal.
- Benjelloun H, et al. (2013). Sarcoidosis in Morocco: review of 120 cases. African Health Sciences.
- Baughman RP, et al. (2021). Sarcoidosis diagnosis and treatment: ATS/ERS/WASOG statement.
Content
Author's details
Reviewer's details
Sarcoidosis
Background
Multisystem granulomatous disorder of unknown aetiology, characterized by non-caseating granulomas. Genetic predisposition with environmental triggers postulated. African Americans have more severe, extrapulmonary disease. African data is limited but suggests different clinical patterns.
African Context: Underreported in Nigeria; most cases diagnosed incidentally. Possibly misdiagnosed as tuberculosis due to clinical and radiological similarities. (Igbokwe et al., 2020; Nigerian Postgraduate Medical Journal)
Further readings
- Igbokwe EU, et al. (2020). Sarcoidosis in Nigeria: A case series and review of challenges. Nigerian Postgraduate Medical Journal.
- Benjelloun H, et al. (2013). Sarcoidosis in Morocco: review of 120 cases. African Health Sciences.
- Baughman RP, et al. (2021). Sarcoidosis diagnosis and treatment: ATS/ERS/WASOG statement.
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