【持续皮下输注奥曲肽治疗伴有糖尿病前期昏迷和尿崩症的肢端肥大症1例】。

T Abe, S Ohguni, K Tanigawa, Y Kato
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引用次数: 0

摘要

一名58岁女性因意识受损、高血糖和双颞偏盲入院。她于一年前被诊断为NIDDM,并接受饮食和格列苯脲(1.25 mg/天)治疗6个月。然而,她在一个月前停止治疗,然后出现多饮和全身疲劳。5天前入院,当时检测到高血糖(405 mg/dl)和贫血(Hb8.0g/dl)。转至我院控制血糖及进一步检查双颞偏盲。她表现出典型的肢端肥大症特征,包括鼻子、嘴唇和舌头的扩大,脚后跟垫和肢端生长的增加。意识障碍通过生理盐水输注和胰岛素治疗。内镜检查显示活动性胃溃疡(A1)。内分泌数据显示血浆和尿液中生长激素水平升高,而血浆IGF-1水平较低。血浆GH在服用TRH后反而增加。缺水试验显示尿渗透压增高,提示部分中枢性尿崩症(DI)。磁共振造影显示大腺瘤向鞍上方向发展。她被诊断为肢端肥大症,部分DI和可能的高渗性高血糖非酮症糖尿病昏迷前期。部分DI引起的多尿(5-101/天)通过给予DDAVP(10微克/天)来控制。持续皮下注射奥曲肽(240微克/天)导致血浆GH水平正常,垂体瘤明显缩小。经奥曲肽治疗4个月后,经蝶窦入路切除垂体瘤。垂体瘤的HE染色显示被玻璃样结缔组织包围的萎缩性嗜酸细胞。术后血浆GH水平恢复正常,并发症治愈。总之,这是一例非常罕见的伴有糖尿病前期昏迷和部分DI的肢端肥大症,持续皮下输注奥曲肽可有效治疗。
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[Effective treatment with constant subcutaneous infusion of octreotide in a patient with acromegaly associated with diabetic pre-coma and diabetes insipidus].

A 58-year-old woman was admitted to our hospital for impaired consciousness, hyperglycemia and bitemporal hemianopsia. She was diagnosed as having NIDDM one year ago and was treated with diet and glibenclamide (1.25 mg/day) for 6 months. However, she stopped her medical treatment one month ago and then polydipsia and general fatigue were manifested. She was admitted to a hospital five days ago at which time hyperglycemia (405 mg/dl) and anemia (Hb8.0g/dl) were detected. She was transferred to our hospital for control of blood glucose and further examination of bitemporal hemianopsia. She showed typical acromegalic features including enlargement of the nose, lips and tongue, increased heel pad and acral growth. Conscious disturbance was cured by the infusion of saline and the administration of insulin. Endoscopy revealed an active gastric ulcer (A1). Endocrine data disclosed increased GH levels in plasma and urine, whereas plasma IGF-1 levels were low. Plasma GH paradoxically increased following the administration of TRH. A water deprivation test showed an impaired increase in urinary osmolarity, indicating partial central diabetes insipidus (DI). MRI with Gd-contrast revealed a macroadenoma which progressed toward suprasella. She was diagnosed as having acromegaly, partial DI and probable hyperosmolar hyperglycemic nonketotic diabetic pre-coma. Polyuria (5-101/day) due to partial DI was controlled by the administration of DDAVP (10 micrograms/day). The constant subcutaneous administration of octreotide (240 micrograms/day) resulted in normal plasma GH levels and a marked shrinkage of the pituitary tumor. The pituitary tumor was finally removed by the transsphenoidal approach following treatment with octreotide for 4 months. HE staining of the pituitary tumor showed atrophic and acidophilic cells surrounded by hyaloid connective tissue. After the surgery, plasma GH levels were normalized and complications were cured. In conclusion, this is a very rare case of acromegaly associated with diabetic pre-coma and partial DI, and effectively treated with constant subcutaneous infusion of octreotide.

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[Parathyroid hormone]. [Treatment of hypothalamic-pituitary tumors--experiences at Hiroshima University School of Medicine]. [Future aspects on endocrinology]. [A view of basic endocrinology]. [Comment by a surgeon on Japan Endocrine Society, its past and future].
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