A patient's autoantibody profile is more informative than the result of any single test for predicting the likelihood of thymoma, and for supporting a diagnosis of MG or other paraneoplastic neurological complication.
Muscle acetylcholine receptor (AChR) and striational autoantibodies are characteristic but not diagnostic of myasthenia gravis (MG) in the context of thymoma. One or more antibodies in the MG/thymoma evaluation are positive in more than 60% of nonimmunosuppressed patients who have thymoma without evidence of any neurological disorder.
Titers of muscle AChR and striational antibodies are generally higher in MG patients who have thymoma, but severity of weakness cannot be predicted by antibody titer. A rising antibody titer (or appearance of a new antibody specificity) following thymoma ablation suggests thymoma recurrence or metastasis, or development of an unrelated neoplasm.
Antibodies specific for the alternative muscle autoantigen of MG, muscle-specific receptor tyrosine kinase, are not associated with thymoma.