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表现为急性胰腺炎和癫痫持续状态的继发性甲状旁腺功能亢进。

Secondary hyperparathyroidism manifesting as acute pancreatitis and status epilepticus.

作者信息

Sallman A, Goldberg M, Wombolt D

出版信息

Arch Intern Med. 1981 Oct;141(11):1549-50.

PMID:7283572
Abstract

A 36-year-old with end-stage renal disease secondary to hypertensive nephrosclerosis had a two-day history of epigastric pain and nausea. Soon after admission, multiple grand mal seizures uncontrolled by intravenous phenytoin sodium and diazepam developed. His calcium level was 14 mg/dL and his amylase level was 2,230 mg/dL; lumbar puncture was normal. Hemodialysis lowered his calcium level to 10.7 mg/dL but failed to control his seizures. Secondary hyperparathyroidism was thought to be the cause of his malignant hypercalcemia, and an emergency subtotal parathyroidectomy was performed. Postoperatively, his grand mal seizures resolved. Confusion and aphasia also developed, but they resolved over the ensuing three weeks. Microscopic examination of the parathyroid glands revealed diffuse chief cell hyperplasia. Preoperative parathormone level was 2,196 pg/dL (normal, less than 450 pg/dL). A review of the literature has failed to reveal a similar case.

摘要

一名36岁因高血压性肾硬化继发终末期肾病的患者,有两天的上腹部疼痛和恶心病史。入院后不久,出现多次癫痫大发作,静脉注射苯妥英钠和地西泮无法控制。他的血钙水平为14mg/dL,淀粉酶水平为2230mg/dL;腰椎穿刺结果正常。血液透析使他的血钙水平降至10.7mg/dL,但未能控制癫痫发作。继发性甲状旁腺功能亢进被认为是其恶性高钙血症的原因,遂进行了急诊甲状旁腺次全切除术。术后,他的癫痫大发作得到缓解。还出现了意识模糊和失语,但在随后的三周内逐渐恢复。甲状旁腺的显微镜检查显示弥漫性主细胞增生。术前甲状旁腺激素水平为2196pg/dL(正常范围小于450pg/dL)。文献检索未发现类似病例。

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