Vestibular Schwannoma
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Neurofibromatosis Type 2 (NF2)
International Journal of Molecular Sciences Review Neurofibromatosis Type 2 (NF2) and the Implications for Vestibular Schwannoma and Meningioma Pathogenesis Suha Bachir 1,† , Sanjit Shah 2,† , Scott Shapiro 3,†, Abigail Koehler 4, Abdelkader Mahammedi 5 , Ravi N. Samy 3, Mario Zuccarello 2, Elizabeth Schorry 1 and Soma Sengupta 4,* 1 Department of Genetics, Cincinnati Children’s Hospital, Cincinnati, OH 45229, USA; [email protected] (S.B.); [email protected] (E.S.) 2 Department of Neurosurgery, University of Cincinnati, Cincinnati, OH 45267, USA; [email protected] (S.S.); [email protected] (M.Z.) 3 Department of Otolaryngology, University of Cincinnati, Cincinnati, OH 45267, USA; [email protected] (S.S.); [email protected] (R.N.S.) 4 Department of Neurology, University of Cincinnati, Cincinnati, OH 45267, USA; [email protected] 5 Department of Radiology, University of Cincinnati, Cincinnati, OH 45267, USA; [email protected] * Correspondence: [email protected] † These authors contributed equally. Abstract: Patients diagnosed with neurofibromatosis type 2 (NF2) are extremely likely to develop meningiomas, in addition to vestibular schwannomas. Meningiomas are a common primary brain tumor; many NF2 patients suffer from multiple meningiomas. In NF2, patients have mutations in the NF2 gene, specifically with loss of function in a tumor-suppressor protein that has a number of synonymous names, including: Merlin, Neurofibromin 2, and schwannomin. Merlin is a 70 kDa protein that has 10 different isoforms. The Hippo Tumor Suppressor pathway is regulated upstream by Merlin. This pathway is critical in regulating cell proliferation and apoptosis, characteristics that are important for tumor progression. -
Surgical Management of Posterior Petrous Meningiomas
Neurosurg Focus 14 (6):Article 7, 2003, Click here to return to Table of Contents Surgical management of posterior petrous meningiomas JAMES K. LIU, M.D., OREN N. GOTTFRIED, M.D., AND WILLIAM T. COULDWELL, M.D., PH.D. Department of Neurosurgery, University of Utah School of Medicine, Salt Lake City, Utah Posterior petrous meningiomas (commonly termed posterior pyramid meningiomas and/or meningiomas of the pos- terior surface of the petrous pyramid) are the most common meningiomas of the posterior cranial fossa. They are locat- ed along the posterior surface of the temporal bone in the region of the cerebellopontine angle. They often mimic vestibular schwannomas, both clinically and on neuroimaging studies. Common clinical symptoms include hearing loss, cerebellar ataxia, and trigeminal neuropathy. The site of dural origin determines the direction of cranial nerve dis- placement. Total resection can be achieved in most cases with a low morbidity rate and an excellent prognosis. The authors review the surgical management of posterior petrous meningiomas. KEY WORDS • meningioma • cerebellopontine angle • skull base surgery • petrous bone Posterior fossa meningiomas comprise approximately In their series Samii and Ammirati18 used the term “pos- 10% of all intracranial meningiomas.8 Castellano and terior pyramid meningiomas” and defined them as tumors Ruggiero4 reviewed Olivecrona’s experience with treat- whose main direction of growth brings them in contact ing posterior fossa meningiomas and classified them with the posterior pyramid, irrespective of their site of based on the site of dural attachment. They described the dural attachment. They also designated those located ante- location as cerebellar convexity (10%), tentorium (30%), rior and those posterior to the internal acoustic meatus. -
(Acoustic Neuroma) After Stereotactic Radiosurgery
Otology & Neurotology 24:650–660 © 2003, Otology & Neurotology, Inc. Clinical and Histopathologic Features of Recurrent Vestibular Schwannoma (Acoustic Neuroma) after Stereotactic Radiosurgery *Daniel J. Lee, *†William H. Westra, ‡Hinrich Staecker, §Donlin Long, and *John K. Niparko Departments of *Otolaryngology-Head and Neck Surgery, †Pathology, and §Neurologic Surgery, The Johns Hopkins School of Medicine; and ‡Division of Otolaryngology–Head and Neck Surgery, Department of Surgery, University of Maryland Medicine, Baltimore, Maryland, U.S.A. Objective: Stereotactic radiosurgery for vestibular schwan- the cerebellopontine angle and internal auditory canal. Fibrosis noma entails uncertain long-term risk of tumor recurrence and outside and within the tumor bed varied markedly, complicat- delayed cranial neuropathies. In addition, the underlying histo- ing microsurgical dissection. Light microscopy confirmed the pathologic changes to the tumor bed are not fully characterized. presence of viable tumor in all cases. Histopathologic features We seek to understand the clinical and histologic features of were typical of vestibular schwannoma, and there was no sig- recurrent vestibular schwannoma after stereotactic radiation nificant scarring that could be attributed to radiation effect. therapy. Conclusions: The variable fibrosis in the cerebellopontine Study Design: Retrospective review. angle and lack of radiation changes seen histopathologically in Setting: Tertiary referral center. irradiated vestibular schwannoma suggest that a uniform -
The Braincase of Two Late Cretaceous Asian Multituberculates Studied by Serial Sections
The braincase of two Late Cretaceous Asian multituberculates studied by serial sections J0RN H. HURUM Hurum, J.H. 1998. The braincase of two Late Cretaceous Asian multituberculatesstudied by serial sections. -Acta Palaeontologica Polonica 43, 1, 21-52. The braincase structure of two Late Cretaceous Mongolian djadochtatherian multituber- culates Nemegtbaatar gobiensis and Chulsanbaatar vulgaris from the ?late Campanian of Mongolia is presented based on the two serially sectioned skulls and additional specimens. Reconstructions of the floor of the braincase in both taxa are given. The complete intracranial sphenoid region is reconstructed for the first time in multitubercu- lates. Cavum epiptericum is a separate space with the taenia clino-orbitalis (ossified pila antotica) as the medial wall, anterior lamina of the petrosal and possibly the alisphenoid as the lateral wall, and the basisphenoid, petrosal and possibly alisphenoid ventrally. The fovea hypochiasmatica is shallow, tuberculurn sellae is wide and more raised from the skull base than it is in the genus Pseudobolodon. The dorsal opening of the carotid canal is situated in the fossa hypophyseos. The taenia clino-orbitalis differs from the one described in Pseudobolodon and Lambdopsalis in possessing just one foramen (metoptic foramen). Compared to all extant mammals the braincase in Nemegtbaatar and Chulsan- baatar is primitive in that both the pila antotica and pila metoptica are retained. In both genera the anterior lamina of the petrosal is large with a long anterodorsal process while the alisphenoid is small. A review is given of the cranial anatomy in Nemegtbaatar and Chulsanbaatar. K e y w o r d s : Braincase structure, sphenoid complex, cavum epiptericum,Mammalia, Multituberculata,Djadochtatheria, Cretaceous, Mongolia. -
Topographical Anatomy and Morphometry of the Temporal Bone of the Macaque
Folia Morphol. Vol. 68, No. 1, pp. 13–22 Copyright © 2009 Via Medica O R I G I N A L A R T I C L E ISSN 0015–5659 www.fm.viamedica.pl Topographical anatomy and morphometry of the temporal bone of the macaque J. Wysocki 1Clinic of Otolaryngology and Rehabilitation, II Medical Faculty, Warsaw Medical University, Poland, Kajetany, Nadarzyn, Poland 2Laboratory of Clinical Anatomy of the Head and Neck, Institute of Physiology and Pathology of Hearing, Poland, Kajetany, Nadarzyn, Poland [Received 7 July 2008; Accepted 10 October 2008] Based on the dissections of 24 bones of 12 macaques (Macaca mulatta), a systematic anatomical description was made and measurements of the cho- sen size parameters of the temporal bone as well as the skull were taken. Although there is a small mastoid process, the general arrangement of the macaque’s temporal bone structures is very close to that which is observed in humans. The main differences are a different model of pneumatisation and the presence of subarcuate fossa, which possesses considerable dimensions. The main air space in the middle ear is the mesotympanum, but there are also additional air cells: the epitympanic recess containing the head of malleus and body of incus, the mastoid cavity, and several air spaces on the floor of the tympanic cavity. The vicinity of the carotid canal is also very well pneuma- tised and the walls of the canal are very thin. The semicircular canals are relatively small, very regular in shape, and characterized by almost the same dimensions. The bony walls of the labyrinth are relatively thin. -
Detection of Calcifications in Retinoblastoma Using Gradient
ORIGINAL RESEARCH HEAD & NECK Detection of Calcifications in Retinoblastoma Using Gradient- Echo MR Imaging Sequences: Comparative Study between In Vivo MR Imaging and Ex Vivo High-Resolution CT F. Rodjan, P. de Graaf, P. van der Valk, T. Hadjistilianou, A. Cerase, P. Toti, M.C. de Jong, A.C. Moll, J.A. Castelijns, and P. Galluzzi, on behalf of the European Retinoblastoma Imaging Collaboration ABSTRACT BACKGROUND AND PURPOSE: Intratumoral calcifications are very important in the diagnosis of retinoblastoma. Although CT is con- sidered superior in detecting calcification, its ionizing radiation, especially in patients with hereditary retinoblastoma, should be avoided. The purpose of our study was to validate T2*WI for the detection of calcification in retinoblastoma with ex vivo CT as the criterion standard. MATERIALS AND METHODS: Twenty-two consecutive patients with retinoblastoma (mean age, 21 months; range, 1–71 months) with enucleation as primary treatment were imaged at 1.5T by using a dedicated surface coil. Signal-intensity voids indicating calcification on T2*WI were compared with ex vivo high-resolution CT, and correlation was scored by 2 independent observers as poor, good, or excellent. Other parameters included the shape and location of the signal-intensity voids. In 5 tumors, susceptibility-weighted images were evaluated. RESULTS: All calcifications visible on high-resolution CT could be matched with signal-intensity voids on T2*WI, and correlation was scored as excellent in 17 (77%) and good in 5 (23%) eyes. In total, 93% (25/27) of the signal-intensity voids inside the tumor correlated with calcifications compared with none (0/8) of the signal-intensity voids outside the tumor. -
Tinnitus: Ringing in the SYMPTOMS Ears
Tinnitus: Ringing in the SYMPTOMS Ears By Vestibular Disorders Association TINNITUS WHAT IS TINNITUS? An abnormal noise perceived in one or both Tinnitus is abnormal noise perceived in one or both ears or in the head. ears or in the head. It Tinnitus (pronounced either “TIN-uh-tus” or “tin-NY-tus”) may be can be experienced as a intermittent, or it might appear as a constant or continuous sound. It can ringing, hissing, whistling, be experienced as a ringing, hissing, whistling, buzzing, or clicking sound buzzing, or clicking sound and can vary in pitch from a low roar to a high squeal. and can vary in pitch. Tinnitus is very common. Most studies indicate the prevalence in adults as falling within the range of 10% to 15%, with a greater prevalence at higher ages, through the sixth or seventh decade of life. 1 Gender distinctions ARTICLE are not consistently reported across studies, but tinnitus prevalence is significantly higher in pregnant than non-pregnant women. 2 The most common form of tinnitus is subjective tinnitus, which is noise that other people cannot hear. Objective tinnitus can be heard by an examiner positioned close to the ear. This is a rare form of tinnitus, 068 occurring in less than 1% of cases. 3 Chronic tinnitus can be annoying, intrusive, and in some cases devastating to a person’s life. Up to 25% of those with chronic tinnitus find it severe DID THIS ARTICLE enough to seek treatment. 4 It can interfere with a person’s ability to hear, HELP YOU? work, and perform daily activities. -
Sporadic Schwannomas and Neurofibromas by Herbert B Newton MD (Dr
Sporadic schwannomas and neurofibromas By Herbert B Newton MD (Dr. Newton, Director of the Neuro-Oncology Center at the Florida Hospital Cancer Institute has no relevant financial relationships to disclose.) Originally released October 15, 1996; last updated March 1, 2017; expires March 1, 2020 Introduction This article includes discussion of sporadic schwannomas and neurofibromas, chitoneuroma, neurilemmoma, perineural fibroblastoma, abducens schwannoma, facial schwannoma, hypoglossal schwannoma, jugular foramen schwannoma, malignant schwannoma, neurofibroma, neurofibrosarcoma, peripheral nerve schwannoma, schwannoma, spinal schwannoma, sporadic neurofibromas, sporadic schwannomas, and trigeminal schwannoma. The foregoing terms may include synonyms, similar disorders, variations in usage, and abbreviations. Overview In this article, the author provides an in-depth review of the pathology, biology, clinical presentation, and treatment options for sporadic schwannomas and neurofibromas. These tumors arise from the nerve sheaths of cranial nerves, nerve roots, spinal nerves, and peripheral nerves. The most common location for schwannomas is the eighth cranial nerve, whereas neurofibromas more commonly arise along the spinal nerve roots. Maximal surgical resection is the treatment of choice for most tumors. Radiotherapy is only used in selected cases. Chemotherapy is still under investigation for therapeutic potential. In this update, the author reviews advances in the molecular biology and therapeutic approaches to these tumors. Key points • Schwannomas are slow-growing extra-axial tumors that can arise from any cranial nerve or spinal nerve root. They most commonly arise from the eighth cranial nerve. • Surgical resection is the treatment option of choice for most tumors. Complete resection can result in a surgical cure. • In selected cases, radiosurgery may be as effective as surgery at local control of tumor growth. -
3.4.12.9 the Temporal Bone of Patient Ip
3.4.12.9 The Temporal Bone of patient Ip Distances (Figure 3.30(n)): Squamous Temporal Bone: The squamous temporal bone was not measurable in this child due to lack of visibility of the asterion (as), sphenion (spt) and the stylomastoid foramen (smÐ. Extemal Auditory Meatus: The configuration of the external auditory meatus was abnormal and asymmetrical, with increased distances recorded on both sides (eampl-pol, pol-eamal, eamir- eampr, eamar-eamir). Zygomatic Process: The length of the zygomatic arch (ztl-aul, ztr-aur) was decreased bilaterally. The articular fossa height (afl-ael, afr-aer) was normal, however, posteriorly the left EAM- articular fossa length (eamal-afl) was increased. Petrous Temporal Bone (Figure 3.30(o)): The prominence of the mastoid process (mal-jfl1, mar-jflr) was increased bilaterally compared with the experimental standard. The distances of the temporal bone showed the right jugular foramen to be narrowed (flr-jfmr) with an similar tendency on the left. The inferior petrous temporo-occipital suture (fml-ptsl, jfrnr-ptsr) was increased in length. Dimensions (Figure 3.30(o)): The petrous temporal ridge distance (petal-petpl, petar-petpr) was increased bilaterally. The dimensions between the temporal bones was increased between the external auditory meatus (pol-por). The angles of the auditory canal (pol-iamViamr-por), the petrous temporal bone angles (petpl-petaVpetar-petpr) and the zygoma projection (petal-aul-ztl, petar-aur-ztr) were not significantly different from the experimental standard. Discussion: Bony distortion was found at the external auditory meatus and the zygomatic arch which was reduced in length. The jugular foramen was nanowed while the temporal occipital suture medially and the distance to the mastoid laterally were increased. -
Acoustic Neuroma
Acoustic Neuroma DISORDERS This document is adapted from materials available from the National Institutes of Health WHAT IS AN ACOUSTIC NEUROMA? VESTIBULAR An acoustic neuroma (also known as vestibular schwannoma or acoustic SCHWANNOMA neurinoma) is a benign (nonmalignant), usually slow-growing tumor that develops from the balance and hearing nerves supplying the inner ear. A benign slow-growing The tumor comes from an overproduction of Schwann cells—the cells that tumor on the normally wrap around nerve fibers to help support and insulate nerves. balance/hearing nerve. HOW DOES IT DEVELOP? As the acoustic neuroma grows, it compresses the hearing and balance nerves, usually causing unilateral (one-sided) hearing loss, tinnitus ARTICLE (ringing in the ear), and dizziness or loss of balance. As it grows, it can also interfere with the facial sensation nerve (the trigeminal nerve), causing facial numbness. It can also exert pressure on nerves controlling the muscles of the face, causing facial weakness or paralysis on the side of the tumor. Vital life-sustaining functions can be threatened when large 03 tumors cause severe pressure on the brainstem and cerebellum. Unilateral acoustic neuromas account for approximately eight percent of all tumors inside the skull; one out of every 100,000 individuals per year develops an acoustic neuroma. Symptoms may develop in individuals DID THIS ARTICLE at any age, but usually occur between the ages of 30 and 60 years. HELP YOU? Unilateral acoustic neuromas are not hereditary. SUPPORT VEDA @ HOW IS IT DIAGNOSED? VESTIBULAR.ORG Early detection of an acoustic neuroma is sometimes difficult because the symptoms related to its early stages may be subtle, if present at all. -
Incidental Vestibular Schwannomas: a Review of Prevalence, Growth Rate, and Management Challenges
Neurosurg Focus 33 (3):E4, 2012 Incidental vestibular schwannomas: a review of prevalence, growth rate, and management challenges RICHARD F. SCHMIDT, B.A.,1 ZAIN BOGHANI, B.S.,1 OSAMAH J. CHOUDHRY, M.D.,1 JEAN ANDErsON ELOY, M.D.,1–3 ROBERT W. JYUNG, M.D.,2,3 AND JAMES K. LIU, M.D.1–3 Departments of 1Neurological Surgery and 2Otolaryngology–Head and Neck Surgery; and 3Center for Skull Base and Pituitary Surgery, Neurological Institute of New Jersey, University of Medicine and Dentistry of New Jersey–New Jersey Medical School, Newark, New Jersey With the relatively recent increase in the use of MRI techniques, there has been a concurrent rise in the number of vestibular schwannomas (VSs) detected as incidental findings. These incidental VSs may be prevalent in up to 0.02%–0.07% of individuals undergoing MRI and represent a significant portion of all diagnosed VSs. The manage- ment of these lesions poses a significant challenge for practitioners. Most incidental VSs tend to be small and as- sociated with minimal symptoms, permitting them to be managed conservatively at the time of diagnosis. However, relatively few indicators consistently predict tumor growth and patient outcomes. Furthermore, growth rates have been shown to vary significantly over time with a large variety of long-term growth patterns. Thus, early MRI screen- ing for continued tumor growth followed by repeated MRI studies and clinical assessments throughout the patient’s life is an essential component in a conservative management strategy. Note that tumor growth is typically associated with a worsening of symptoms in patients who undergo conservative management, and many of these symptoms have been shown to significantly impact the patient’s quality of life. -
Hemorrhagic Vestibular Schwannoma: an Unusual Clinical Entity Case Report
Neurosurg Focus 5 (3):Article 9, 1998 Hemorrhagic vestibular schwannoma: an unusual clinical entity Case report Dean Chou, M.D., Prakash Sampath, M.D., and Henry Brem, M.D. Departments of Neurological Surgery and Neuro-Oncology, The Johns Hopkins Hospital, Baltimore, Maryland Hemorrhagic vestibular schwannomas are rare entities, with only a few case reports in the literature during the last 25 years. The authors review the literature on vestibular schwannoma hemorrhage and the presenting symptoms of this entity, which include headache, nausea, vomiting, sudden cranial nerve dysfunction, and ataxia. A very unusual case is presented of a 36-year-old man, who unlike most of the patients reported in the literature, had clinically silent vestibular schwannoma hemorrhage. The authors also discuss the management issues involved in more than 1000 vestibular schwannomas treated at their institution during a 25-year period. Key Words * acoustic tumor * schwannoma * neuroma * hemorrhage * hemorrhagic vestibular tumor Vestibular schwannomas are the most common tumors found in the cerebellopontine angle (CPA), comprising approximately 80% of all tumors arising in this region. They are usually slow-growing, benign tumors that manifest clinically by directly compressing the neural elements traversing the CPA, including the pons, cerebellum, and the lower cranial nerves. Hemorrhage into a vestibular schwannoma is rare and has been shown to present with acute neurological changes and deterioration. We review the literature on the presenting symptoms of hemorrhagic vestibular schwannomas and describe the case of a man with a large hemorrhagic vestibular schwannoma who presented with signs and symptoms of a slow-growing, insidious compressive lesion. In doing so, we hope to shed light on this unusual clinical entity and discuss management issues.