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肢端肥大症伴神经节细胞瘤。

Acromegaly associated with gangliocytoma.

机构信息

Academic Department of Endocrinology, Beaumont Hospital, Dublin 9, Ireland.

出版信息

Ir J Med Sci. 2012 Sep;181(3):353-5. doi: 10.1007/s11845-009-0433-2. Epub 2009 Sep 30.

Abstract

BACKGROUND

Acromegaly secondary to growth hormone-releasing hormone (GHRH) excess is rare.

AIMS/CASE DESCRIPTION: We report two patients with acromegaly who were diagnosed with sellar gangliocytomas that were immunopositive for GHRH. Tumour tissue persisted after debulking surgery and in the second case this was associated with persistent growth hormone hypersecretion, successfully suppressed by a somatostatin analogue.

CONCLUSIONS

The development of functional pituitary adenomas in association with sellar gangliocytomas is poorly understood. We present a brief discussion of the possible aetiology of these unusual pituitary tumours.

摘要

背景

生长激素释放激素(GHRH)过多引起的肢端肥大症较为罕见。

目的/病例描述:我们报告了两例因生长激素释放激素免疫阳性而被诊断为鞍结节神经节细胞瘤的肢端肥大症患者。肿瘤组织在肿瘤切除术之后仍然存在,在第二种情况下,这与持续的生长激素分泌过多有关,使用生长抑素类似物成功抑制了这种分泌过多。

结论

与鞍结节神经节细胞瘤相关的功能性垂体腺瘤的发展机制尚不清楚。我们简要讨论了这些不常见的垂体肿瘤的可能病因。

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