Al-Sharafi Butheinah A, Nassar Omar H
Department of Medicine, School of Medicine and Health Sciences, Sana'a University, P.O Box 12268, Sana'a, Yemen.
Case Rep Obstet Gynecol. 2013;2013:817603. doi: 10.1155/2013/817603. Epub 2013 Sep 30.
Pituitary apoplexy is a rare condition which may cause death of the patient in severe cases and many times leads to hypopituitarism. We report a case of apoplexy in a large prolactinoma resulting in empty sella syndrome followed by a successful pregnancy. Our patient is a 32-year-old female with a history of a macroprolactinoma for approximately 17 years who presented to our hospital with a history of severe headache, decreased level of consciousness, fever, nausea, vomiting, and diplopia of 12 hours duration. Magnetic resonance imaging done on admission showed an increase in the size of the pituitary adenoma with a subtle hemorrhage. The patient was admitted to the intensive care unit and treated conservatively. The condition of the patient improved within a few days. A few months later, she started having regular menstrual periods. A magnetic resonance imaging of the pituitary 1.5 years later was reported as empty sella syndrome, and approximately one year later she became pregnant. With the pituitary adenoma being resolved after developing pituitary apoplexy and continuing on cabergoline, the patient had a successful pregnancy with no recurrence of the adenoma after delivery and breastfeeding.
垂体卒中是一种罕见的病症,在严重情况下可能导致患者死亡,且多次会引发垂体功能减退。我们报告一例大泌乳素瘤发生卒中导致空蝶鞍综合征,随后成功妊娠的病例。我们的患者是一名32岁女性,有大约17年的大泌乳素瘤病史,因严重头痛、意识水平下降、发热、恶心、呕吐及持续12小时的复视前来我院就诊。入院时进行的磁共振成像显示垂体腺瘤体积增大并有轻微出血。患者被收入重症监护病房并接受保守治疗。患者的病情在数天内有所改善。几个月后,她开始有规律的月经周期。1.5年后垂体的磁共振成像报告为空蝶鞍综合征,大约一年后她怀孕了。垂体卒中后垂体腺瘤消退并继续服用卡麦角林,患者成功妊娠,分娩和哺乳后腺瘤未复发。