Long-term follow-up of acoustic neuromas by serial MRI scans

1999 ◽  
Vol 121 (2_suppl) ◽  
pp. P116-P116
Author(s):  
Hinrich Staecker ◽  
Joseph B Nadol ◽  
Michael J McKenna
2021 ◽  
Vol 11 ◽  
Author(s):  
Yu Zhang ◽  
Jianfei Long ◽  
Junwei Ren ◽  
Xiang Huang ◽  
Ping Zhong ◽  
...  

Vestibular schwannomas (VSs, also known as acoustic neuromas) are relatively rare benign brain tumors stem from the Schwann cells of the eighth cranial nerve. Tumor growth is the paramount factor for neurosurgeons to decide whether to choose aggressive treatment approach or careful follow-up with regular magnetic resonance imaging (MRI), as surgery and radiation can introduce significant trauma and affect neurological function, while tumor enlargement during long-term follow-up will compress the adjacent nerves and tissues, causing progressive hearing loss, tinnitus and vertigo. Recently, with the deepening research of VS biology, some proteins that regulate merlin conformation changes, inflammatory cytokines, miRNAs, tissue proteins and cerebrospinal fluid (CSF) components have been proposed to be closely related to tumor volume increase. In this review, we discuss advances in the study of biomarkers that associated with VS growth, providing a reference for exploring the growth course of VS and determining the optimal treatment strategy for each patient.


2019 ◽  
Vol 130 (2) ◽  
pp. 388-397 ◽  
Author(s):  
Josa M. Frischer ◽  
Elise Gruber ◽  
Verena Schöffmann ◽  
Adolf Ertl ◽  
Romana Höftberger ◽  
...  

OBJECTIVEThe authors present long-term follow-up data on patients treated with Gamma Knife radiosurgery (GKRS) for acoustic neuroma.METHODSSix hundred eighteen patients were radiosurgically treated for acoustic neuroma between 1992 and 2016 at the Department of Neurosurgery, Medical University Vienna. Patients with neurofibromatosis and patients treated too recently to attain 1 year of follow-up were excluded from this retrospective study. Thus, data on 557 patients with spontaneous acoustic neuroma of any Koos grade are presented, as are long-term follow-up data on 426 patients with a minimum follow-up of 2 years. Patients were assessed according to the Gardner-Robertson (GR) hearing scale and the House-Brackmann facial nerve function scale, both prior to GKRS and at the times of follow-up.RESULTSFour hundred fifty-two patients (81%) were treated with radiosurgery alone and 105 patients (19%) with combined microsurgery-radiosurgery. While the combined treatment was especially favored before 2002, the percentage of cases treated with radiosurgery alone has significantly increased since then. The overall complication rate after GKRS was low and has declined significantly in the last decade. The risk of developing hydrocephalus after GKRS increased with tumor size. One case (0.2%) of malignant transformation after GKRS was diagnosed. Radiological tumor control rates of 92%, 91%, and 91% at 5, 10, and 15 years after GKRS, regardless of the Koos grade or pretreatment, were observed. The overall tumor control rate without the need for additional treatment was even higher at 98%. At the last follow-up, functional hearing was preserved in 55% of patients who had been classified with GR hearing class I or II prior to GKRS. Hearing preservation rates of 53%, 34%, and 34% at 5, 10, and 15 years after GKRS were observed. The multivariate regression model revealed that the GR hearing class prior to GKRS and the median dose to the cochlea were independent predictors of the GR class at follow-up.CONCLUSIONSIn small to medium-sized spontaneous acoustic neuromas, radiosurgery should be recognized as the primary treatment at an early stage. Although minimizing the cochlear dose seems beneficial for hearing preservation, the authors, like others before, do not recommend undertreating intracanalicular tumors in favor of low cochlear doses. For larger acoustic neuromas, radiosurgery remains a reliable management option with tumor control rates similar to those for smaller acoustic neuromas; however, careful patient selection and counseling are recommended given the higher risk of side effects. Microsurgery must be considered in acoustic neuromas with significant brainstem compression or hydrocephalus.


2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
Cheng Huan ◽  
Chao Lu ◽  
Guang-ming Xu ◽  
Xin Qu ◽  
Yuan-ming Qu

Objective. We compared the characteristics of patients with Cushing’s disease alone with those of patients with Cushing’s disease and hyperprolactinemia.Methods. Eighty-four patients were enrolled between 2002 and 2011, in a hospital in China. Clinical, endocrinological, and histopathological data, MRI scans, and surgical outcomes were reviewed throughout the follow-up period.Results. Patients with Cushing’s disease and hyperprolactinemia had a younger age at diagnosis (30.28 ± 14.23 versus 36.08 ± 10.91 years;P=0.037) and a larger adenoma maximal diameter (2.44 ± 1.32 versus 1.44 ± 1.05 cm;P<0.001) than patients with Cushing’s disease alone. Menstrual disorders (P=0.027) and visual field defects (P=0.021) were more common and progressive obesity (P=0.009) and hypertension (P<0.001) were less common in patients with Cushing’s disease and hyperprolactinemia. The rate of normalization of hormonal levels was lower (41.7% versus 91.7%;P<0.001) and the recurrence rate was higher (36.1% versus 8.3%;P<0.001) in patients with Cushing’s disease and hyperprolactinemia.Conclusions. Careful long-term follow-up is needed of patients with Cushing’s disease and hyperprolactinemia.


1995 ◽  
Vol 37 (6) ◽  
pp. 427-428 ◽  
Author(s):  
S. Terao ◽  
G. Sobue ◽  
N. Shimada ◽  
M. Takahashi ◽  
Y. Tsuboi ◽  
...  

PLoS ONE ◽  
2020 ◽  
Vol 15 (12) ◽  
pp. e0244672
Author(s):  
Giosuè Mascioli ◽  
Elena Lucca ◽  
Federica Michelotti ◽  
Luca Tarantino ◽  
Fabrizio Giofré ◽  
...  

1995 ◽  
Vol 37 (6) ◽  
pp. 427-428
Author(s):  
S. Terao ◽  
G. Sobue ◽  
N. Shimada ◽  
M. Takahashi ◽  
Y. Tsuboi ◽  
...  

2019 ◽  
Vol 42 ◽  
Author(s):  
John P. A. Ioannidis

AbstractNeurobiology-based interventions for mental diseases and searches for useful biomarkers of treatment response have largely failed. Clinical trials should assess interventions related to environmental and social stressors, with long-term follow-up; social rather than biological endpoints; personalized outcomes; and suitable cluster, adaptive, and n-of-1 designs. Labor, education, financial, and other social/political decisions should be evaluated for their impacts on mental disease.


2001 ◽  
Vol 120 (5) ◽  
pp. A397-A397
Author(s):  
M SAMERAMMAR ◽  
J CROFFIE ◽  
M PFEFFERKORN ◽  
S GUPTA ◽  
M CORKINS ◽  
...  

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