Table 2.
Key Pathological Features of Sarcoidosis
Favors Sarcoidosis | Against Sarcoidosis |
---|---|
Granuloma presence | |
Numerous | Few |
Absent but with nodular hyalinized fibrosis representing healed granulomas (scattered multinucleated giant cells may be detectable) | Absent |
Granuloma morphology | |
Compact, tightly formed collections of large “epithelioid” histiocytes and multinucleated giant cells. Granulomas tend to stay discrete | Loosely organized collections of mononuclear phagocytes/multinucleated giant cells |
Nonnecrotic or focal and usually minimal ischemic necrosis | • Extensive necrosis |
• Dirty necrosis (containing nuclear debris) | |
• Palisading granulomas | |
Fibrosis beginning at the granuloma periphery with extension centrally into the granuloma, with or without calcification | |
Lesion location | |
Perilymphatic; around bronchovascular bundles and fibrous septa containing pulmonary veins, and near visceral pleura | • Lack of lymphangitic distribution |
• Intraalveolar granulomas | |
In necrotizing sarcoid angiitis and granulomatosis: granulomatous angiitis with invasion of vascular walls | |
| |
Accompanying histology | |
Sparse surrounding lymphocytic infiltrate | • Robust surrounding inflammatory infiltrate (including lymphocytes, neutrophils, eosinophils, and plasma cells) |
• Secondary lymphoid follicles | |
Microorganism stains and cultures | |
Negative | Positive |
Multidisciplinary clinical features | |
Intra- and extrathoracic involvement | Extrathoracic involvement only |