Sugihara Hitoshi
Department of Endocrinology, Diabetes and Metabolism, Nippon Medical School.
J Nippon Med Sch. 2017;84(5):201-208. doi: 10.1272/jnms.84.201.
The number of cases of lymphocytic hypophysitis is small, although the condition is not rare. For optimal therapy, the correct diagnosis from imaging, immunological studies, and pathological findings from a pituitary biopsy is important. Recently, anti-Rabphilin antibody has been proposed to be a biomarker for lymphocytic infundibulo-neurohypophysitis. Immunological disorders such as anti-Pit-1 antibody syndrome are similar to the pathogenesis of lymphocytic hypophysitis. Moreover, recent immune checkpoint blockade such ipilimumab has been shown to induce anti-CTLA-4-related hypophysitis. In the future, elucidating the immunological mechanism and establishing a suitable therapy will be necessary for accurate long-term prognosis.
淋巴细胞性垂体炎的病例数量较少,尽管这种病症并不罕见。为了实现最佳治疗,通过影像学、免疫学研究以及垂体活检的病理结果进行正确诊断至关重要。最近,抗Rabphilin抗体被认为是淋巴细胞性漏斗神经垂体炎的一种生物标志物。诸如抗Pit-1抗体综合征等免疫紊乱与淋巴细胞性垂体炎的发病机制相似。此外,最近已表明,诸如伊匹单抗等免疫检查点阻断剂可诱发抗CTLA-4相关的垂体炎。未来,阐明免疫机制并建立合适的治疗方法对于准确的长期预后将是必要的。