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. 2020 Apr 30;58(2):93–100. doi: 10.5114/reum.2020.95363

Table I.

Differential diagnosis of sarcoidosis

A. Systemic and organ-specific manifestations of sarcoidosis
 Lymphoproliferative diseases
 Sarcoid-like reaction to malignancy
 Infectious diseases, including:
  tuberculosis
  atypical mycobacterial infections
  brucellosis
  coccidioidomycosis and other fungal diseases
  leishmaniosis
 Silicosis
 Pneumoconiosis
 Beryllium hypersensitivity
 Talc or zirconium exposure
 Drug-induced granulomatosis
 Interstitial lung disease
 Autoimmune disorders
 Blau syndrome and other autoinflammatory syndromes
 Common variable immune deficiency
B. Musculoskeletal manifestations of sarcoidosis
 Bone metastasis
 Multiple myeloma
 Osseous hemangiomas
 Enchondromas (Ollier disease, Maffucci syndrome)
 Paget’s disease
 Osteopetrosis
 Osteopoikilosis (including Buschke-Ollendorff syndrome)
 Hyperparathyroidism and other bone metabolic disorders
 Vitamin D-resistant rickets (X-linked hypophosphatemia)
 Mastocytosis
 Bone tuberculosis
 Brucellosis with joint and bone involvement
 Coccidioidomycosis with musculoskeletal involvement (desert rheumatism)
 Inflammatory spondyloarthropathy
 Muscular metastases
 Muscular infarction (including that resulting from diabetes mellitus)
 Inflammatory myopathy including regional forms