Department of Neurosurgery, University Medical Center Göttingen, Georg-August-University Göttingen, Germany.
Department of Neurosurgery, Mashhad University of Medical Sciences, Mashhad, Iran.
Urology. 2014 Apr;83(4):756-61. doi: 10.1016/j.urology.2013.12.018. Epub 2014 Feb 16.
To provide the first insights into the potential role of skull base chordoma, which causes brainstem compression in and around Barrington's nucleus and its effect on the micturition center. Chordoma is a rare malignant bone tumor that originates from the remnants of the embryonic notochord, which normally forms and dissolves during early fetal development. Although it is a slowly growing tumor, it displays local invasive growth.
Urodynamic testing of 22 symptomatic patients was performed. All women and men with skull base chordoma treated in 2 hospitals in Germany between 1986 and 2007 were studied. Follow-up periods ranged from 6 months to 10 years. Lower urinary tract symptoms were documented in patients with acute brainstem compression because of local chordoma growth.
Of 74 patients treated, 22 (7 women, 15 men) with a median age of 37 years were evaluated with voiding diaries and computer urodynamic investigation. Urodynamic testing of 22 symptomatic patients revealed detrusor overactivity in 55%, low compliance bladder in 14%, detrusor-sphincter dyssynergia in 45%, and uninhibited sphincter relaxation in 27%. Despite the description of incomplete emptying and urgency, 4 patients had normal urodynamic findings (18%). Brain magnetic resonance images of the lesions of the symptomatic patients were obtained to determine the side of lesions.
The dorsolateral pons, including pontine reticular nucleus and the reticular formation and the locus coeruleus, seems to be mainly responsible for lower urinary tract symptoms in our patients with skull base chordoma and brainstem compression.
首次探讨颅底脊索瘤的潜在作用,该肿瘤可导致延髓及 Barrington 核周围的脑干受压,并影响排尿中枢。脊索瘤是一种罕见的恶性骨肿瘤,起源于胚胎脊索的残留物,脊索在胎儿早期发育过程中正常形成和溶解。尽管它是一种生长缓慢的肿瘤,但具有局部侵袭性生长的特点。
对 22 例有症状的患者进行尿动力学检查。研究了 1986 年至 2007 年间在德国 2 家医院治疗的所有患有颅底脊索瘤的女性和男性患者。随访时间为 6 个月至 10 年。由于局部脊索瘤生长导致急性脑干压迫,记录下患者的下尿路症状。
在 74 例接受治疗的患者中,有 22 例(7 名女性,15 名男性)中位年龄为 37 岁,通过排尿日记和计算机尿动力学检查进行了评估。对 22 例有症状的患者进行尿动力学检查,发现逼尿肌过度活动占 55%,顺应性膀胱低占 14%,逼尿肌括约肌协同失调占 45%,无抑制性括约肌松弛占 27%。尽管有不完全排空和急迫性的描述,但仍有 4 例患者的尿动力学检查结果正常(18%)。对有症状患者的病变进行脑磁共振成像以确定病变的侧别。
我们的颅底脊索瘤和脑干压迫患者的下尿路症状主要与桥脑背外侧,包括桥脑网状核和网状结构以及蓝斑有关。