Background
At present, thyrotropin-secreting pituitary adenoma (TSHoma) is recognized as a rare disease. Mixed TSHomas accounted for 20-25% of all TSHomas. This study aimed to report an extremely rare case of mixed TSHoma coexisted with Graves’ disease(GD) and review the literature.
Case presentation
A 36-year-old male patient presented with both elevated levels of free triiodothyronine (FT3), free thyroxine (FT4) and insulin-like growth factor 1 (IGF-1), but non-suppressed thyroid-stimulating hormone (TSH) level. His anti-thyroglobulin antibody (TGAb), anti-thyroid peroxidase autoantibody (TPOAb), and thyrotropin receptor antibody (TRAb) were positive. The symptoms of palpitations, hyperhidrosis, heat intolerant, and irritability appeared 2 years before his admission. But he showed neither signs nor symptoms of acromegaly. Contrast-enhanced pituitary magnetic resonance imaging (MRI) showed enlarged pituitary fossa, with an irregular abnormal signal mass. The patient underwent endoscopic partial pituitary resection via transsphenoidal approach. Postoperative pathology suggested mixed pituitary adenoma. The patient had postoperative thyroid function recurrence of hyperthyroidism and the recurrence of TSHoma was confirmed by positron emission tomography-computed tomography (PET-CT) 11months after surgery. After administration of lanreotide, his levels of FT3, FT4, TSH, TPOAb and TGAb became normal, and levels of TRAb and IGF-1 improved.
Conclusion
A rare case of TSHoma coexisted with GD was reported. When circulating levels of both FT4 and FT3 were upregulated, non-suppressed TSH levels and positive thyroid antibodies were found. Importantly, TSHoma associated with GD should be carefully taken into account to avoid the potential risk of treatment-induced tumor progression.