López J, Barceló B, Lucas T, Salame F, Alameda C, Boronat M, Salto L, Estrada J
Department of Endocrinology, Universidad Autónoma de Madrid, Spain.
Clin Endocrinol (Oxf). 1996 Aug;45(2):147-56. doi: 10.1046/j.1365-2265.1996.d01-1550.x.
While inferior petrosal sinus (IPS) sampling correctly diagnoses pituitary-dependent Cushing's syndrome if a significant ratio of plasma ACTH between the IPS and the peripheral blood is demonstrated, little has been said about the significance of a negative ratio in Cushing's disease (e.g. a false-negative result). This study evaluates the results of IPS sampling in patients with Cushing's disease, and compares them with both imaging findings and transsphenoidal examination.
The results of IPS sampling were retrospectively compared with both imaging findings and transsphenoidal examination. IPS samples were obtained before and 2, 5 and 10 minutes after intravenous administration of 100 micrograms of CRH.
Thirty-two patients with Cushing's disease were evaluated. All subsequently underwent transphenoidal examination of the pituitary gland.
The ratio of the ACTH concentrations at the IPS and in the peripheral blood (IPS:P ratio), and the ratio of the ACTH concentrations between the IPSs (interpetrosal ratio) were calculated. Radiographic evaluation of the pituitary gland was performed with magnetic resonance imaging (MRI, 29 cases) or computed tomography imaging (CT, 3 cases).
Transsphenoidal examination of the pituitary gland revealed a microadenoma in 27 cases. Radiological imaging showed a signal compatible with a microadenoma in 22 cases (68.8%), and correctly located the tumour at the side found at surgery in 14 of the 22 cases with positive transsphenoidal findings (MRI 13 cases, CT 1 case, overall 63.6%). Successful bilateral catheterization was accomplished in 30 patients (93.8%). Samples before and after CRH stimulation were drawn in 24 cases. No major complications were observed with the technique. IPS catheterization correctly predicted Cushing's disease (by means of a significant IPS: P ACTH ratio) in 27 of the 30 patients (90%) with basal sampling, and in 23 of the 24 cases with samples drawn before and after CRH administration (95.8%). Taking into account the 12 patients with a lateral microadenoma shown at transsphenoidal examination, IP sinus ACTH ratio was in agreement with the side recorded by the neurosurgeon in 8/12 cases (66.7%). MRI correctly located the tumour in 8/12 patients (66.7%). One patient showed no significant IPS: P ACTH ratio in any set of samples. His MRI showed no sign of a microadenoma. Two years later, another pituitary MRI evaluation showed a midline hypodense signal. The transsphenoidal examination revealed a microadenoma and the post-operative plasma cortisol and urinary free cortisol fell to 293 nmol/l and 100 nmol/24 h, respectively.
Only when a significant IPS:P ACTH ratio is present can Cushing's disease be established by IPS sampling. The absence of a significant IPS: P ACTH ratio does not necessarily imply ectopic secretion of ACTH, nor does it exclude Cushing's disease. The results of lateralization by IPS sampling do not remove the need for a thorough transsphenoidal examination of the contents of the sella turcica.
如果岩下窦(IPS)与外周血中血浆促肾上腺皮质激素(ACTH)存在显著比例,则岩下窦采血可正确诊断垂体依赖性库欣综合征,但关于库欣病中阴性比例的意义(如假阴性结果)却鲜有提及。本研究评估库欣病患者岩下窦采血的结果,并将其与影像学检查结果及经蝶窦检查结果进行比较。
对岩下窦采血结果与影像学检查结果及经蝶窦检查结果进行回顾性比较。在静脉注射100微克促肾上腺皮质激素释放激素(CRH)之前及之后2、5和10分钟采集岩下窦样本。
对32例库欣病患者进行评估。所有患者随后均接受了垂体的经蝶窦检查。
计算岩下窦与外周血中ACTH浓度的比值(IPS:P比值)以及两侧岩下窦之间ACTH浓度的比值(岩下窦间比值)。采用磁共振成像(MRI,29例)或计算机断层扫描成像(CT,3例)对垂体进行影像学评估。
垂体经蝶窦检查发现27例存在微腺瘤。影像学检查显示22例(68.8%)有与微腺瘤相符的信号,在22例经蝶窦检查阳性的病例中,有14例(MRI 13例,CT 1例,总体63.)的肿瘤位置与手术发现的一侧相符。30例患者(93.8%)成功进行了双侧置管。24例患者在CRH刺激前后采集了样本。该技术未观察到重大并发症。在30例进行基础采血的患者中,有27例(90%)通过显著的IPS:P ACTH比值,岩下窦置管正确预测了库欣病;在24例在CRH给药前后采集样本的病例中,有23例(95.8%)正确预测。考虑到经蝶窦检查显示为侧方微腺瘤的12例患者,岩下窦ACTH比值与神经外科医生记录的一侧在其中8/12例(66.7%)中相符。MRI在8/12例患者(66.7%)中正确定位了肿瘤。1例患者在任何一组样本中均未显示出显著的IPS:P ACTH比值。其MRI未显示微腺瘤迹象。两年后,另一次垂体MRI评估显示中线低密度信号。经蝶窦检查发现微腺瘤,术后血浆皮质醇和尿游离皮质醇分别降至293 nmol/l和100 nmol/24 h。
只有当存在显著的IPS:P ACTH比值时,才能通过岩下窦采血确诊库欣病。IPS:P ACTH比值不显著并不一定意味着ACTH的异位分泌,也不排除库欣病。岩下窦采血的定位结果并不能消除对蝶鞍内容物进行全面经蝶窦检查的必要性。