Extraordinary case presentations in pediatric pituitary adenoma: report of 6 cases

被引:0
作者
Meyer, Jenna [1 ]
Perry, Avital [1 ]
Oushy, Soliman [1 ]
Graffeo, Christopher S. [1 ]
Carlstrom, Lucas P. [1 ]
Meyer, Fredric B. [1 ]
机构
[1] Mayo Clin, Dept Neurol Surg, Rochester, MN USA
关键词
pediatric; adenoma; prolactinoma; extraordinary; pituitary surgery; INTERNAL CAROTID-ARTERY; CUSHINGS-DISEASE; TRANSSPHENOIDAL SURGERY; CORTISOL-LEVELS; HORMONE EXCESS; OCCLUSION; MANAGEMENT; CHILDHOOD; GIGANTISM; CHILDREN;
D O I
10.3171/2019.7.PEDS1950
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
A 14-year-old girl presented with acute hemiparesis and aphasia. MRI revealed a pituitary macroadenoma causing internal carotid artery invasion/obliteration without acute apoplexy, which was treated via emergent transsphenoidal resection (TSR). Another 14-year-old girl developed precocious galactorrhea due to macroprolactinoma, which was medically managed. Several years later, she re-presented with acute, severe, bitemporal hemianopia during her third trimester of pregnancy, requiring emergent induction of labor followed by TSR. A 13-year-old boy was incidentally diagnosed with a prolactinoma after routine orthodontic radiographs captured a subtly abnormal sella. An 18-year- old male self-diagnosed pituitary gigantism through a school report on pituitary disease. A 17-year-old boy was diagnosed with Cushing disease by his basketball coach, a former endocrinologist. A 12-year-old girl with growth arrest and weight gain was diagnosed with Cushing disease, which was initially treated via TSR but subsequently recurred and ultimately required 12 operations, 5 radiation treatments involving 3 modalities, bilateral adrenalectomy, and chemotherapy. Despite these efforts, she ultimately died from pituitary carcinoma.
引用
收藏
页码:43 / 50
页数:8
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