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 |