30 research outputs found

    Risk of intracranial meningioma in patients with acromegaly: a systematic review

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    Acromegaly is a rare endocrine disorder caused by hypersecretion of growth hormone (GH) from a pituitary adenoma. Elevated GH levels stimulate excess production of insulin-like growth factor 1 (IGF-1) which leads to the insidious onset of clinical manifestations. The most common primary central nervous system (CNS) tumors, meningiomas originate from the arachnoid layer of the meninges and are typically benign and slow-growing. Meningiomas are over twice as common in women as in men, with age-adjusted incidence (per 100,000 individuals) of 10.66 and 4.75, respectively. Several reports describe co-occurrence of meningiomas and acromegaly. We aimed to determine whether patients with acromegaly are at elevated risk for meningioma. Investigation of the literature showed that co-occurrence of a pituitary adenoma and a meningioma is a rare phenomenon, and the majority of cases involve GH-secreting adenomas. To the best of our knowledge, a systematic review examining the association between meningiomas and elevated GH levels (due to GH-secreting adenomas in acromegaly or exposure to exogenous GH) has never been conducted. The nature of the observed coexistence between acromegaly and meningioma -whether it reflects causation or mere co-association -is unclear, as is the pathophysiologic etiology.Systematic review registrationhttps://www.crd.york.ac.uk/prospero/, identifier CRD42022376998

    Anaplastic pleomorphic xanthoastrocytoma with spinal leptomeningeal spread at the time of diagnosis in an adult

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    We describe the first patient, to our knowledge, with anaplastic pleomorphic xanthoastrocytoma (PXA) with spinal leptomeningeal spread at the time of diagnosis and present a review of the literature. PXA is a tumor that typically has an indolent course but occasionally, when anaplastic features are present, behaves in a more aggressive manner. We found that PXA with spinal leptomeningeal spread at the time of diagnosis confers a worse prognosis. Craniospinal imaging should be obtained at time of diagnosis of PXA and the presence of leptomeningeal spread may be indicative of a more aggressive disease process

    Determinants of Surgical Remission in Prolactinomas: A Systematic Review and Meta-Analysis

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    Objective: Prolactin-secreting tumors respond well to medical management, with a few patients requiring surgery. We conducted a systematic review and meta-analysis to study the determinants of surgical remission in these tumors. Methods: We searched PubMed to identify eligible studies reporting postoperative remission in patients treated with transsphenoidal surgery for prolactinoma. Primary outcomes included postoperative remission, follow-up remission, and recurrence. Postoperative and follow-up remission were defined as normoprolactinemia at 1 year after operation, respectively. Recurrence was defined as hyperprolactinemia after initial normalization of prolactin levels. Odds ratios (ORs) were calculated, stratified by radiologic size, tumor extension, and tumor invasion, and analyzed using a random-effects model meta-analysis. Results: Thirty-five studies were included. Macroadenomas were associated with lower rates of postoperative remission (OR, 0.20; 95% confidence interval [CI], 0.16–0.24) and lower rates of remission at follow-up (OR, 0.11; 95% CI, 0.053–0.22). Postoperative remission was less likely in tumors with extrasellar or suprasellar extension (OR, 0.16; 95% CI, 0.06–0.43) and tumors with cavernous sinus invasion (OR, 0.03; 95% CI, 0.01–0.13). Female gender and absence of preoperative dopamine agonist treatment were also associated with higher remission rates. Across the included studies, there was considerable heterogeneity in each primary outcome (postoperative remission, I2 = 94%; follow-up remission, I2 = 86%; recurrence, I2 = 68%). Conclusions: Transsphenoidal surgery for prolactinomas may be particularly effective in small, noninvasive, treatment-naive tumors and may provide a viable first-line alternative to dopamine agonist therapy in such patients

    Postoperative Sinus Thrombosis in the Setting of Skull Base Surgery

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    Objective: Cerebral venous sinus thrombosis (CVST) is a rare but potentially dangerous complication following craniotomies involving the posterior fossa, the skull base, and craniotomies involving the superior sagittal sinus. Surgical manipulation of the sinuses has been shown to cause sinus thromboses of varying degrees. This phenomenon is often clinically silent, with only a small number of patients becoming symptomatic. Recent advances in neuroimaging provide higher resolution evaluation of cerebral sinuses pre and postoperatively, often revealing clinically silent filling defects. Although sinus thrombosis can be a major cause of morbidity and mortality, its incidence and factors that contribute to its formation in the post-operative population remain unclear. In addition, current guidelines advise to anticoagulate with Heparin upon diagnosis, which can be contraindicated for immediate post craniotomy patients. The goal of this study is to evaluate retrospective data of patient outcomes and factors that might contribute to sinus thrombus formation. Methods: A retrospective chart review was conducted at NYU Langone Medical Center. Ninety-seven patients were included who underwent either a retrosigmoid/translabrynthine/suboccipital resection of a posterior fossa tumor or a supratentorial craniotomy for resection of parasagittal/falcine tumor between July 1, 2014 and July 1, 2015. Pre operative Magnetic Resonance Venography (MRV) was obtained per the attending surgeon’s discretion. Based on intraoperative findings, clinical symptoms, and surgeon’s preference, a postoperative MRV was obtained. Decision to treat a thrombosis was made based on the results of the MRV and clinical symptoms. Treatments included observation, intravenous fluids (IVF) alone, anti-platelet therapy with Aspirin alone, or a combination of the two. Results: A total of 7 of 97 patients (7.22%) had postoperative sinus thrombosis. Of those patients, 5 had occlusion of the venous sinuses. In the occlusion group, 4 had preoperative imaging documenting patency of the sinuses. An additional 2 patients had postoperative MRVs revealing partial thrombosis of the sinus, 1 that was new and 1 that did not have a preoperative MRV for comparison. Compared with the cohort of patients without postoperative thromboses, there was no significant difference in age, BMI, length of surgery, or surgical approach. Of the 5 patients with postoperative thrombotic occlusion, 4 underwent intervention (1 with IVF alone, 2 with IVF and aspirin, and 1 with aspirin alone). Two patients with thromboses also developed CSF leaks requiring lumbar drainage and operative repair. One patient had a persistent CSF leak requiring a shunt. Of the 2 patients with partial thrombosis, 1 was placed on IVF and aspirin. At 3 months follow up, 1 out of 5 patients in the occlusion group had recanalization of the previously thrombosed sinus. Conclusions: MRV is a non-invasive method to evaluate the caliber and patency of dural venous sinuses in post craniotomy patients. Symptomatic thrombosis is rare and can be managed either conservatively or with IVF and/or anti platelet therapy, both which are safer than anticoagulation with heparin in post craniotomy patients. A larger prospective trial is necessary to further characterize the incidence of postoperative venous sinus thrombosis, identify risk factors, and to devise recommendations for therapy
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