Vaphiades Michael S, Simmons Debra, Archer Robert L, Stringer Warren
Department of Ophthalmology, University of Alabama-Birmingham, Suite 601, 700 South 18th Street, Birmingham, AL 35233, USA.
Surv Ophthalmol. 2003 Mar-Apr;48(2):230-3. doi: 10.1016/s0039-6257(02)00459-9.
A 40-year-old woman presented with headache and diplopia after hypotension from postpartum hemorrhage. A noncontrasted cranial magnetic resonance imaging (MRI) showed an enlarged pituitary with a rim of slight increased signal. A repeat gadolinium-enhanced cranial MRI showed peripheral enhancement of the pituitary gland surrounding an isointense central area consistent with infarction of the pituitary and the clinical diagnosis of Sheehan syndrome. The patient was treated with intravenous hydrocortisone. Immediately after treatment, her symptoms remitted and the examination normalized. One month later, a gadolinium-enhanced cranial MRI was normal. The characteristic appearance of the post-gadolinium enhanced cranial MRI helped confirm the diagnosis of Sheehan syndrome and facilitate early treatment with corticosteroids.
一名40岁女性在产后出血导致低血压后出现头痛和复视。非增强头颅磁共振成像(MRI)显示垂体增大,边缘信号略有增加。重复钆增强头颅MRI显示垂体周围强化,中央等信号区符合垂体梗死,临床诊断为希恩综合征。患者接受了静脉注射氢化可的松治疗。治疗后症状立即缓解,检查结果恢复正常。1个月后,钆增强头颅MRI正常。钆增强头颅MRI的特征性表现有助于确诊希恩综合征,并促进早期使用皮质类固醇治疗。