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垂体手术后鞍区血肿:临床及生化特征

Postoperative sellar hematoma after pituitary surgery: clinical and biochemical characteristics.

作者信息

El-Asmar Nadine, El-Sibai Katia, Al-Aridi Ribal, Selman Warren R, Arafah Baha M

机构信息

Division of Clinical and Molecular EndocrinologyCase Medical Center and Case Western Reserve University, Cleveland, OH, USA.

The Department of Neurological SurgeryCase Medical Center and Case Western Reserve University, Cleveland, OH, USA.

出版信息

Eur J Endocrinol. 2016 May;174(5):573-82. doi: 10.1530/EJE-15-0961. Epub 2016 Feb 5.

Abstract

BACKGROUND

Postoperative sellar hematoma can develop following surgery for pituitary tumors and other sellar masses such a Rathke's cleft cyst (RCC) due to continued blood oozing. Though often mild sellar hematoma can create mass effects that might impair pituitary function.

AIM

This study summarizes the clinical and biochemical characteristics of sellar hematoma and explores the potential mechanisms for the associated hypopituitarism.

PATIENTS AND METHODS

Sellar hematoma was suspected clinically (worsening headaches, visual impairment, and mental status alterations) and confirmed radiographically in 23 patients (18/279 with macroadenomas and in 5/92 with RCC). Postoperatively, patients were monitored without glucocorticoid therapy and all had appropriately normal HPA function before sellar hematoma diagnosis.

RESULTS

The demographics of patients who had sellar hematoma were similar to those who did not. Biochemical changes at diagnosis included decreased plasma ACTH and its dependent steroids (cortisol, DHEA, and DHEA-S), concomitant mild hyperprolactinemia, and mild hyponatremia (P < 0.005 for all parameters). Treatment with glucocorticoids resulted in rapid clinical improvement in most patients. Glucocorticoid therapy was discontinued within 2 weeks and re-testing thereafter showed normal HPA function in 16/23. None of the patients without sellar hematoma had worsening in pituitary function, visual, or neurological symptoms.

CONCLUSIONS

When large, sellar hematoma can lead to mass effect that causes headaches, visual symptoms, and acute and often reversible hypopituitarism manifesting initially as impaired HPA function. Rapid resolution is observed in most patients with glucocorticoid administration The rapid onset and reversibility of hypopituitarism associated with mild hyperprolactinemia suggest that compression of pituitary stalk/ portal vessels is likely the dominant mechanism of pituitary dysfunction in this setting.

摘要

背景

垂体肿瘤及其他鞍区肿物(如拉克氏囊肿,RCC)手术后,因持续渗血可形成鞍区血肿。尽管鞍区血肿通常较轻,但可产生占位效应,进而损害垂体功能。

目的

本研究总结鞍区血肿的临床及生化特征,并探讨相关垂体功能减退的潜在机制。

患者与方法

临床怀疑鞍区血肿(头痛加重、视力障碍及精神状态改变)的23例患者经影像学检查确诊(18例为大腺瘤患者,占279例大腺瘤患者中的18例;5例为RCC患者,占92例RCC患者中的5例)。术后,在未给予糖皮质激素治疗的情况下对患者进行监测,且所有患者在鞍区血肿诊断前HPA功能均正常。

结果

发生鞍区血肿的患者人口统计学特征与未发生者相似。诊断时的生化改变包括血浆促肾上腺皮质激素(ACTH)及其依赖的类固醇激素(皮质醇、脱氢表雄酮及硫酸脱氢表雄酮)水平降低,同时伴有轻度高催乳素血症及轻度低钠血症(所有参数P<0.005)。大多数患者接受糖皮质激素治疗后临床症状迅速改善。糖皮质激素治疗在2周内停用,之后再次检测显示23例患者中有16例HPA功能正常。无鞍区血肿的患者垂体功能、视力或神经症状均未恶化。

结论

鞍区血肿较大时可导致占位效应,引起头痛、视觉症状以及最初表现为HPA功能受损的急性且通常可逆的垂体功能减退。大多数接受糖皮质激素治疗的患者症状迅速缓解。垂体功能减退的快速发生及可逆性,以及轻度高催乳素血症表明,在此情况下垂体柄/门脉血管受压可能是垂体功能障碍的主要机制。

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