Department of Neurological Surgery, University of Miami Miller School of Medicine, Lois Pope LIFE Center, 1095 NW 14th Terrace (D4-6), Miami, FL 33136, USA.
Pituitary. 2012 Mar;15(1):101-5. doi: 10.1007/s11102-010-0244-5.
A 41-year-old man presented with left optic neuritis (ON) without evidence of other autoimmune disease or hormonal imbalance. MRI showed enlargement of the left optic nerve but no sellar lesion. The patient recovered after steroid therapy but later developed right ON and required treatment again. Follow-up MRI revealed an ill-defined, enlarging sellar lesion with enhancement extending into the right cavernous sinus, and the patient developed symptoms of fatigue and loss of libido. Hormonal studies revealed hypogonadism and hypocortisolism. All laboratory investigation for autoimmune and infectious diseases remained negative. A transsphenoidal biopsy of the lesion revealed lymphocytic hypophysitis. The concomitant development of lymphocytic hypophysitis and optic neuritis suggests a common and likely autoimmune etiology. Visual loss in patients with LYH can sometimes be due to ON rather than compression of the optic apparatus, with significant implications for treatment strategies.
一位 41 岁男性以左眼视神经炎(ON)就诊,无其他自身免疫性疾病或激素失衡的证据。MRI 显示左眼视神经增粗,但蝶鞍区无病变。患者接受类固醇治疗后恢复,但后来又出现右眼 ON,需要再次治疗。随访 MRI 显示蝶鞍区边界不清的增大病变,伴有增强效应延伸至右侧海绵窦,患者出现疲劳和性欲减退的症状。激素研究显示性腺功能减退和皮质醇功能减退。所有自身免疫性和感染性疾病的实验室检查均为阴性。病变的经蝶窦活检显示淋巴细胞性垂体炎。淋巴细胞性垂体炎和视神经炎的同时发生提示存在共同的、可能的自身免疫病因。LYH 患者的视力丧失有时可能是由于 ON 而不是视神经受压所致,这对治疗策略有重要影响。