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. 2019 Aug 2;3(3):358–375. doi: 10.1016/j.mayocpiqo.2019.04.006

Table 2.

Diagnosis of Neurosarcoidosis

Diagnosis Criteria Additional comments
Definite Suggestive clinical presentation of neurosarcoidosis None
Plus
Positive histology of nervous system Presence of sarcoid-type granulomas with epithelioid cells and macrophages without necrosis in the center, surrounded by lymphocytes, plasma cells, and mast cells in tissue biopsied from nervous system
Plus
Exclusion of other possible diagnoses None
Probable Suggestive clinical presentation of neurosarcoidosis None
Plus
Evidence of inflammation in central nervous system Elevated protein and/or cells and/or oligoclonal band in cerebrospinal fluid
OR
Abnormalities on brain magnetic resonance imaging compatible with neurosarcoidosis
Plus
Evidence of systemic sarcoidosis Presence of sarcoid-type granulomas with epithelioid cells and macrophages without necrosis in the center, surrounded by lymphocytes, plasma cells, and mast cells in tissue biopsied from extraneural organs
OR
At least 2 indirect evidences from gallium scan, chest imaging, and elevated angiotensin-converting enzyme level
Plus
Exclusion of other possible diagnoses None
Possible Suggestive clinical presentation of neurosarcoidosis with exclusion of other diseases when the criteria for definite and probable diagnosis are not met None

Data from QJM.47