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1.
J Laryngol Otol ; 138(3): 310-314, 2024 Mar.
Article En | MEDLINE | ID: mdl-37462121

OBJECTIVE: Functional endoscopic sinus surgery for chronic rhinosinusitis improves sinus drainage and intranasal medication delivery. This study compares medication delivery with commonly used devices in normal and altered anatomy (post functional endoscopic sinus surgery) using sinus surgery models (Phacon). METHODS: Medication delivery was simulated via nasal drops, nasal spray and an irrigation device (Neilmed Sinus Rinse). Coverage was then calculated from endoscopic pictures taken at various anatomical sites in the normal nose and post functional endoscopic sinus surgery. RESULTS: In the normal nose, nasal spray did not penetrate the sphenoid sinus, and drops bypassed the vestibule anteriorly. Neilmed Sinus Rinse provided superior coverage at the sphenoid site following sphenoidectomy and the frontal site following Draf III. After ethmoidectomy, nasal drops overall provided less coverage than the other methods. CONCLUSION: Neilmed Sinus Rinse generally provided the best distribution, followed by the nasal spray and then nasal drops. The type and extent of surgery also affects medication delivery.


Paranasal Sinuses , Rhinitis , Sinusitis , Humans , Nasal Sprays , Sinusitis/drug therapy , Sinusitis/surgery , Sphenoid Sinus , Endoscopy , Paranasal Sinuses/surgery , Chronic Disease , Rhinitis/drug therapy , Rhinitis/surgery
2.
BMJ Open ; 13(2): e061349, 2023 02 20.
Article En | MEDLINE | ID: mdl-36806133

OBJECTIVE: To establish consensus definitions for necrotising otitis externa (NOE) to facilitate the diagnosis and exclusion of NOE in clinical practice and expedite future high-quality study of this neglected condition. DESIGN: The work comprised of a systematic review of the literature, five iterative rounds of consultation via a Delphi process and open discussion within the collaborative. An expert panel analysed the results to produce the final outputs which were shared with and endorsed by national specialty bodies. SETTING: Secondary care in the UK. PARTICIPANTS: UK clinical specialists practising in infection, ear nose and throat (ENT) surgery or radiology. MAIN OUTCOME MEASURES: Definitions and statements meeting the following criteria were accepted: (a) minimum of 70% of respondents in agreement or strong agreement with a definition/statement AND (b) <15% of respondents in disagreement or strong disagreement with a definition/statement. RESULTS: Seventy-four UK clinicians specialising in ENT, Infection and Radiology with a special interest in NOE took part in the work which was undertaken between 2019 and 2021. The minimum response rate for a Round was 76%. Consensus criteria for all proposed case definitions, outcome definitions and consensus statements were met in the fifth round. CONCLUSIONS: This work distills the clinical opinion of a large group of multidisciplinary specialists from across the UK to create practical definitions and statements to support clinical practice and research for NOE. This is the first step in an iterative process. Further work will seek to validate and test these definitions and inform their evolution.


Otitis Externa , Radiology , Humans , Otitis Externa/diagnosis , Delphi Technique , Consensus , United Kingdom
3.
Can J Ophthalmol ; 58(2): 113-117, 2023 04.
Article En | MEDLINE | ID: mdl-34715034

OBJECTIVE: Silent sinus syndrome (SSS) usually manifests clinically as hypoglobus and enophthalmos. Patients may experience different symptoms and may present to an assortment of specialties and delay diagnosis and management. The objective of this article was to describe the different and sometimes misleading signs and symptoms of SSS to improve the level of suspicion and reduce time to diagnosis. METHODS: A retrospective consecutive audit of the records of all patients diagnosed with SSS between 2015 and 2019 in the Oxford Eye Hospital, Oxford University Hospitals NHS Foundation Trust. Demographic and clinical data including presentation, diagnosis, and symptoms were obtained from the patients' medical files. RESULTS: Ten patients were included; mean age was 42.5 ± 11.5 years (range, 16-56 years). Four patients were initially referred to an ophthalmologist with globe asymmetry, diplopia, eyelid asymmetry, or retraction. Three patients were initially referred to an ear, nose, and throat specialist with facial asymmetry or infraorbital paraesthesia. Two patients were referred from the maxillofacial department with an incidental finding, and the last patient was seen initially by the neurology team with headaches. CONCLUSION: SSS has a variable presentation. Patients may have common or misleading signs. Patients may attend different clinics and subspecialties, and physicians should be aware of the broad range of presenting signs in this condition to prevent delay in diagnosis and further morbidity.


Enophthalmos , Paranasal Sinus Diseases , Humans , Adult , Middle Aged , Retrospective Studies , Tomography, X-Ray Computed , Syndrome , Maxillary Sinus , Enophthalmos/diagnosis , Enophthalmos/etiology , Paranasal Sinus Diseases/diagnosis
4.
World Neurosurg ; 150: 171, 2021 06.
Article En | MEDLINE | ID: mdl-33838335

The pterygopalatine fossa (PPF) is an inverted, pyramid-shaped space immediately behind the posterior wall of the maxillary sinus, and lesions arising here include juvenile angiofibromas, schwannomas, and, in exceptionally rare cases, malignant peripheral nerve sheath tumors.1,2 Surgical access to the PPF is challenging and has been historically achieved via an open transmaxillary approach associated with facial scaring/deformity as well as potential injury to facial and infraorbital nerve branches.3 We present the case of a 67-year-old woman with facial numbness secondary to a presumed trigeminal schwannoma in the right PPF on magnetic resonance imaging. This surgical video highlights the key stages in performing an endoscopic endonasal excision of a PPF tumor. We start with a wide medial maxillary antrostomy, mobilization of the inferior turbinate, ethmoidectomy, and sphenoidotomy. The posterior wall of the maxillary sinus is then lifted off the anterior aspect of the tumor. The soft tissue attachment medial to the tumor containing the sphenopalatine artery is then cauterized and divided. This is followed by circumferential blunt dissection of the tumor until it is sufficiently mobile to remove in a piecemeal fashion. The PPF is then examined for any residual tumor and any bleeding from the maxillary artery within the fat pad. Hemostasis and reattachment of the inferior turbinate into the lateral nasal wall is demonstrated. The patient did not have any new deficits postoperatively, but histology indicated a malignant peripheral nerve sheath tumor and she underwent postoperative proton beam therapy. Postoperative surveillance magnetic resonance imaging at 14 months showed no tumor recurrence. The patient consented to the procedure in a standard fashion (Video 1).


Neuroendoscopy/methods , Neurofibrosarcoma/surgery , Pterygopalatine Fossa/surgery , Aged , Female , Humans , Maxillary Sinus/surgery , Pterygopalatine Fossa/pathology , Treatment Outcome
5.
Cureus ; 12(10): e11175, 2020 Oct 26.
Article En | MEDLINE | ID: mdl-33262912

Carotid artery dissection (CAD) is a haemorrhage into the arterial wall disrupting the intimal layers of the vessel. We present a case of a 16-year-old male with a non-traumatic spontaneous CAD. The patient presented with Horner's syndrome following an episode of orbital cellulitis secondary to sinusitis requiring sinus drainage surgery. Subsequent magnetic resonance imaging (MRI) revealed a CAD. The patient was treated with antiplatelet medication.

6.
Turk Arch Otorhinolaryngol ; 58(4): 254-267, 2020 Dec.
Article En | MEDLINE | ID: mdl-33554201

This review examines the latest evidence for photodynamic therapy (PDT) in treating chronic rhinosinusitis. MedLine, EMBASE and TRIP Database searches were conducted using the terms: "photodynamic" or "phototherapy" or "photo" and "sinusitis" or "rhinosinusitis," date range January 2000 to May 2020. A total of 192 records were initially identified, after duplicates and exclusions, 9 full papers and 3 abstracts were included. All study types including in-vitro, animal and human studies were evaluated. Whilst there is in-vitro evidence for the efficacy of PDT's bactericidal effect on drug resistant bacteria and biofilm viability, there are few clinical studies. PDT is a promising area of research, but larger, focused studies looking at the safety, delivery, efficacy, and patient selection are required before it can be considered a viable treatment for CRS.

8.
AME Case Rep ; 2: 47, 2018.
Article En | MEDLINE | ID: mdl-30596202

Opsoclonus myoclonus syndrome (OMS) is a rare neurological condition causing rapid jerking involuntary eye movements and myoclonus. The combination of opsoclonus and myoclonus have led to condition being coined the "dancing eyes, dancing feet syndrome". There are a wide variety of paraneoplastic and para-infectious aetiologies for OMS and therefore a detailed workup is needed as OMS symptoms can precede the commencement of symptoms from the underlying triggering disease process. In this case report, we present a case of sphenoid sinusitis in a pregnant lady. We detail her presentation, investigatory work-up and treatment. We also review the pathophysiological theories that can lead to OMS in the current literature.

9.
Cochrane Database Syst Rev ; 12: CD004328, 2018 Dec 31.
Article En | MEDLINE | ID: mdl-30596479

BACKGROUND: Epistaxis (nosebleed) most commonly affects children and the elderly. The majority of episodes are managed at home with simple measures. In more severe cases medical intervention is required to either cauterise the bleeding vessel, or to pack the nose with various materials. Tranexamic acid is used in a number of clinical settings to stop bleeding by preventing clot breakdown (fibrinolysis). It may have a role in the management of epistaxis as an adjunct to standard treatments, reducing the need for further intervention. OBJECTIVES: To determine the effects of tranexamic acid (oral, intravenous or topical) compared with placebo, no additional intervention or any other haemostatic agent in the management of patients with epistaxis. SEARCH METHODS: The Cochrane ENT Information Specialist searched the Cochrane ENT Register (via CRS Web); Central Register of Controlled Trials (CENTRAL) (via CRS Web); PubMed; Ovid Embase; CINAHL; Web of Science; ClinicalTrials.gov; ICTRP and additional sources for published and unpublished trials. The date of the search was 29 October 2018. SELECTION CRITERIA: Randomised controlled trials (RCTs) of tranexamic acid (in addition to usual care) compared with usual care plus placebo, usual care alone or usual care plus any other haemostatic agent, to control epistaxis in adults or children. DATA COLLECTION AND ANALYSIS: We used the standard methodological procedures expected by Cochrane. The primary outcomes were control of epistaxis: re-bleeding (as measured by the proportion of patients re-bleeding within a period of up to 10 days) and significant adverse effects (seizures, thromboembolic events). Secondary outcomes were control of epistaxis as measured by the time to stop initial bleeding (the proportion of patients whose bleeding is controlled within a period of up to 30 minutes); severity of re-bleeding (as measured by (a) the proportion of patients requiring any further intervention and (b) the proportion of patients requiring blood transfusion); length of hospital stay and other adverse effects. We used GRADE to assess the quality of the evidence for each outcome; this is indicated in italics. MAIN RESULTS: We included six RCTs (692 participants). The overall risk of bias in the studies was low. Two studies assessed oral administration of tranexamic acid, given regularly over several days, and compared it to placebo. In the other four studies, a single application of topical tranexamic acid was compared with placebo (one study) and a combination of epinephrine and lidocaine or phenylephrine (three studies). All participants were adults.Tranexamic acid versus placeboFor our primary outcome, control of epistaxis: re-bleeding (proportion re-bleeding within 10 days), we were able to pool data from three studies. The pooled result demonstrated a benefit of tranexamic acid compared to placebo, the risk of re-bleeding reducing from 67% to 47% (risk ratio (RR) 0.71, 95% confidence interval (CI) 0.56 to 0.90; three studies; 225 participants; moderate-quality evidence).When we compared the effects of oral and topical tranexamic acid separately the risk of re-bleeding with oral tranexamic acid reduced from 69% to 49%, RR 0.73 (95% CI 0.55 to 0.96; two studies, 157 participants; moderate-quality evidence) and with topical tranexamic acid it reduced from 66% to 43%, RR 0.66 (95% CI 0.41 to 1.05; single study, 68 participants). We rated the quality of evidence provided by the single study as low, therefore it is uncertain whether topical tranexamic acid is effective in stopping bleeding in the 10-day period after a single application.No study specifically sought to identify and report our primary outcome: significant adverse effects (i.e. seizures, thromboembolic events).The secondary outcome time to stop initial bleeding (proportion with bleeding controlled within 30 minutes) was measured in one study using topical tranexamic acid and there was no evidence of a difference at 30 minutes (RR 0.79, 95% CI 0.56 to 1.11; 68 participants; low-quality evidence).No studies reported the proportion of patients requiring any further intervention (e.g. repacking, surgery, embolisation).One study of oral tranexamic acid reported the proportion of patients requiring blood transfusion and found no difference between groups: 5/45 (11%) versus 6/44 (14%) (RR 0.81, 95% CI 0.27 to 2.48; 89 participants; low-quality evidence).Two studies reported hospital length of stay. One study reported a significantly shorter stay in the oral tranexamic acid group (mean difference (MD) -1.60 days, 95% CI -2.49 to -0.71; 68 participants). The other study found no evidence of a difference between the groups.Tranexamic acid versus other haemostatic agentsWhen we pooled the data from three studies the proportion of patients whose bleeding stopped within 10 minutes was significantly higher in the topical tranexamic acid group compared to the group receiving another haemostatic agent (70% versus 30%: RR 2.35, 95% CI 1.90 to 2.92; 460 participants) (moderate-quality evidence).Adverse effects across all studiesFive studies recorded 'adverse effects' in a general way. None found any difference between the groups in the occurrence of minor adverse effects (e.g. mild nausea and diarrhoea, 'bad taste' of gel). In one study a patient developed a superficial thrombophlebitis of both legs following discharge, however it is not reported in which group this occurred. No "other serious adverse effect" was reported in any study. AUTHORS' CONCLUSIONS: We found moderate-quality evidence that there is probably a reduction in the risk of re-bleeding with the use of either oral or topical tranexamic acid in addition to usual care in adult patients with epistaxis, compared to placebo with usual care. However, the quality of evidence relating solely to topical tranexamic acid was low (one study only), so we are uncertain whether or not topical tranexamic acid is effective in stopping bleeding in the 10-day period after a single application. We found moderate-quality evidence that topical tranexamic acid is probably better than other topical agents in stopping bleeding in the first 10 minutes.There have been only three RCTs on this subject since 1995. Since then there have been significant changes in nasal cauterisation and packing techniques (for example, techniques including nasal endoscopy and more invasive approaches such as endoscopic sphenopalatine artery ligation). New trials would inform us about the effectiveness of tranexamic acid in light of these developments.


Antifibrinolytic Agents/therapeutic use , Epistaxis/drug therapy , Tranexamic Acid/therapeutic use , Administration, Oral , Administration, Topical , Antifibrinolytic Agents/administration & dosage , Antifibrinolytic Agents/adverse effects , Blood Transfusion/statistics & numerical data , Epinephrine/therapeutic use , Humans , Length of Stay , Lidocaine/therapeutic use , Phenylephrine/therapeutic use , Placebos/therapeutic use , Randomized Controlled Trials as Topic , Recurrence , Secondary Prevention/statistics & numerical data , Tranexamic Acid/administration & dosage , Tranexamic Acid/adverse effects
11.
J Emerg Med ; 47(3): e69-72, 2014 Sep.
Article En | MEDLINE | ID: mdl-24915744

BACKGROUND: Orbital injury secondary to petroleum-based products is rare. We report the first case, to our knowledge, of a combined compressed air and chemical orbital injury, which mimicked necrotizing fasciitis. CASE REPORT: A 58-year-old man was repairing his motorcycle engine when a piston inadvertently fired, discharging compressed air and petroleum-based carburetor cleaner into his left eye. He developed surgical emphysema, skin necrosis, and a chemical cellulitis, causing an orbital compartment syndrome. He was treated initially with antibiotics and subsequently with intravenous steroid and orbital decompression surgery. There was almost complete recovery by 4 weeks postsurgery. WHY SHOULD AN EMERGENCY PHYSICIAN BE AWARE OF THIS?: Petroleum-based products can cause severe skin irritation and necrosis. Compressed air injury can cause surgical emphysema. When these two mechanisms of injury are combined, the resulting orbitopathy and skin necrosis can mimic necrotizing fasciitis and cause diagnostic confusion. A favorable outcome is achievable with aggressive timely management.


Blast Injuries/complications , Compressed Air/adverse effects , Eye Injuries, Penetrating/etiology , Fasciitis, Necrotizing/chemically induced , Orbit/injuries , Orbital Diseases/chemically induced , Petroleum/adverse effects , Subcutaneous Emphysema/etiology , Humans , Male , Middle Aged
13.
J Craniomaxillofac Surg ; 41(8): 850-5, 2013 Dec.
Article En | MEDLINE | ID: mdl-23485485

Tension pneumocephalus is a rare, but potentially life-threatening complication of transcranial surgery. Whilst commonly described in the field of neurosurgery, little has been published in the context of craniofacial surgery. We describe two cases of post-operative extradural tension pneumocephalus occurring following free myocutaneous latissimus dorsi flap reconstruction of anterior cranial defects following extirpation of advanced recurrent skin carcinomas. These cases illustrate the variation in clinical presentation of this condition, the importance of prompt recognition, urgent radiological investigation and timely decompression, and potential management strategies for minimising the risk of recurrent symptoms.


Carcinoma/surgery , Facial Neoplasms/surgery , Free Tissue Flaps/adverse effects , Myocutaneous Flap/adverse effects , Neoplasm Recurrence, Local/surgery , Paranasal Sinus Neoplasms/surgery , Plastic Surgery Procedures/adverse effects , Pneumocephalus/surgery , Postoperative Complications/surgery , Skin Neoplasms/surgery , Aged , Dura Mater/surgery , Follow-Up Studies , Free Tissue Flaps/transplantation , Frontal Sinus/surgery , Humans , Male , Middle Aged , Myocutaneous Flap/transplantation , Neoplasm Invasiveness , Orbital Neoplasms/surgery , Radiography, Interventional , Recurrence , Suction/methods , Tomography, X-Ray Computed/methods
14.
Cochrane Database Syst Rev ; (7): CD005232, 2011 Jul 06.
Article En | MEDLINE | ID: mdl-21735400

BACKGROUND: This is an update of a Cochrane Review first published in The Cochrane Library in Issue 1, 2007.Benign nasal polyps are lesions that arise from the mucosa of the nasal cavity or one or more of the nasal sinuses. The presenting symptoms are nasal obstruction, watery anterior rhinorrhoea (excessive nasal secretions) or mucopurulent postnasal drip (or both), hyposmia and anosmia (reduced or absent sense of smell) with a concomitant alteration in taste and infrequently pain over the dorsum of the nose, forehead and cheeks. The main aim of treatment is to relieve these symptoms. The aetiology of polyps is uncertain, therefore treatment options differ, consisting of a combination of medical and surgical management. Medical therapy is mainly in the form of steroids, administered topically or systemically via the oral route. OBJECTIVES: To assess the effects of oral steroids in patients with multiple nasal polyps. SEARCH STRATEGY: We searched the Cochrane Ear, Nose and Throat Disorders Group Trials Register; the Cochrane Central Register of Controlled Trials (CENTRAL); PubMed; EMBASE; CINAHL; Web of Science; BIOSIS Previews; Cambridge Scientific Abstracts; ISRCTN and additional sources for published and unpublished trials. The date of the most recent search was 12 October 2010, following a previous search in April 2006. SELECTION CRITERIA: Randomised controlled trials and controlled clinical trials comparing oral steroids with no intervention, or placebo, or comparing doses or schedules of oral steroids in patients with multiple nasal polyps. DATA COLLECTION AND ANALYSIS: Two authors independently assessed study quality. We contacted study authors for additional information. MAIN RESULTS: Three trials (166 patients) met our inclusion criteria and showed a short-term benefit of a short (two to four-week) course of oral steroids of variable doses and duration when compared to placebo. There was an objective reduction of polyp size and a subjective improvement of nasal symptoms and quality of life. However, due to the moderate to low quality of these trials it was not possible to quantify the overall size of this effect.There was no report of significant adverse effects of treatment with a short course of steroids. AUTHORS' CONCLUSIONS: The authors found three randomised controlled trials, albeit of moderate to poor quality, that suggest a short-term benefit of oral steroids in patients with multiple nasal polyps. To address the issue more thoroughly well-designed, prospective, randomised controlled trials are still needed.


Nasal Polyps/drug therapy , Prednisone/administration & dosage , Steroids/administration & dosage , Administration, Oral , Humans , Nasal Obstruction/etiology , Nasal Polyps/complications , Olfaction Disorders/etiology , Randomized Controlled Trials as Topic
15.
Int J Pediatr Otorhinolaryngol ; 74(12): 1438-40, 2010 Dec.
Article En | MEDLINE | ID: mdl-20870298

We present the case of a mother and four children displaying signs of Multiple Synostosis Syndrome (SYNS1) associated with conductive hearing loss. The intra-familial phenotypic variation is due to variable penetrance, which is typical of this syndrome. The child with the most significant hearing loss showed lucency of the otic capsule on temporal bone CT. There is no evidence of this phenomenon associated with SYNS1 in the literature. CT scanning can diagnose certain ossicular chain abnormalities, removing the need for tympanotomy under general anaesthetic. Syndromic hearing loss is progressive and should be monitored where appropriate.


Ear Ossicles/diagnostic imaging , Hearing Loss, Conductive/genetics , Syndactyly/genetics , Synostosis/genetics , Tomography, X-Ray Computed , Adult , Child , Child, Preschool , Female , Hearing Loss, Conductive/diagnosis , Hearing Loss, Conductive/diagnostic imaging , Humans , Male , Syndrome , Temporal Bone/diagnostic imaging
16.
Cochrane Database Syst Rev ; (9): CD005233, 2010 Sep 08.
Article En | MEDLINE | ID: mdl-20824844

BACKGROUND: This is an update of a Cochrane Review originally published in Issue 1, 2007 of The Cochrane Library.Tinnitus is an auditory perception that can be described as the experience of sound, in the ear or in the head, in the absence of external acoustic stimulation. Cognitive behavioural therapy (CBT) uses relaxation, cognitive restructuring of the thoughts and exposure to exacerbating situations in order to promote habituation and may benefit tinnitus patients, as may the treatment of associated psychological conditions. OBJECTIVES: To assess whether CBT is effective in the management of patients suffering from tinnitus. SEARCH STRATEGY: We searched the Cochrane Ear, Nose and Throat Disorders Group Trials Register; the Cochrane Central Register of Controlled Trials (CENTRAL); PubMed; EMBASE; CINAHL; Web of Science; BIOSIS Previews; Cambridge Scientific Abstracts; PsycINFO; ISRCTN and additional sources for published and unpublished trials. The date of the most recent search was 6 May 2010. SELECTION CRITERIA: Randomised controlled trials in which patients with unilateral or bilateral tinnitus as their main symptom received cognitive behavioural treatment. DATA COLLECTION AND ANALYSIS: One review author (PMD) assessed every report identified by the search strategy. Three authors (PMD, AW and MT) assessed the methodological quality and applied inclusion/exclusion criteria. Two authors (PMD and RP) extracted data and conducted the meta-analysis. The four authors contributed to the final text of the review. MAIN RESULTS: Eight trials comprising 468 participants were included.For the primary outcome of subjective tinnitus loudness we found no evidence of a difference between CBT and no treatment or another intervention (yoga, education and 'minimal contact - education').In the secondary outcomes we found evidence that quality of life scores were improved in participants who had tinnitus when comparing CBT to no treatment or another intervention (education and 'minimal contact education'). We also found evidence that depression scores improved when comparing CBT to no treatment. We found no evidence of benefit in depression scores when comparing CBT to other treatments (yoga, education and 'minimal contact - education').There were no adverse/side effects reported in any trial. AUTHORS' CONCLUSIONS: In six studies we found no evidence of a significant difference in the subjective loudness of tinnitus.However, we found a significant improvement in depression score (in six studies) and quality of life (decrease of global tinnitus severity) in another five studies, suggesting that CBT has a positive effect on the management of tinnitus.


Cognitive Behavioral Therapy/methods , Tinnitus/therapy , Humans , Quality of Life , Randomized Controlled Trials as Topic
17.
Skull Base ; 18(1): 1-8, 2008 Jan.
Article En | MEDLINE | ID: mdl-18592018

OBJECTIVE: To evaluate the management of patients with malignant tumors of the ear and temporal bone. DESIGN: Retrospective analysis of data. SETTING: Radcliffe Infirmary, Oxford, United Kingdom. PARTICIPANTS: Twenty-seven patients were classified into two groups according to the site of origin of the tumor: (1) superficial (17 tumors): tumors arising from the skin of the pinna, parotid, and temporomandibular joint area; (2) deep (10 tumors): tumors arising in the ear canal and temporal bone. MAIN OUTCOME MEASURES: Treatment modality, complications, recurrence rate, disease-free interval, and survival. RESULTS: The mean follow-up period was 25 months (0 to 60), and the median overall survival 46 months (0 to 102). Complications occurred in 6 patients (22%). The 3-year survival was 38% (95% confidence interval [CI], 19 to 58%), and the 5-year survival 19% (95% CI, 3 to 35%). CONCLUSIONS: There were insufficient data to demonstrate any difference in survival or disease-free interval related to the site of tumor origin (superficial versus deep tumors). There were independent differences in survival in favor of both performing parotidectomy and using postoperative radiotherapy, but neither reached significance at the 0.05 level.

18.
Ear Nose Throat J ; 85(6): 392-6, 2006 Jun.
Article En | MEDLINE | ID: mdl-16866118

Malignant peripheral nerve sheath tumors are uncommon lesions that occasionally affect the head and neck. We describe 2 new cases of head and neck pathology. One tumor involved the parotid gland and resulted in erosion of the temporal bone, and the other affected the lower lip. A rapid diagnosis has significant implications for management because of the tumor's potential for aggressive behavior and its high rate of recurrence. To the best of our knowledge, lip involvement is rare and temporal bone involvement has not been previously described.


Lip Neoplasms/diagnosis , Nerve Sheath Neoplasms/diagnosis , Parotid Neoplasms/diagnosis , Adult , Angiography , Hearing Loss, Sensorineural/etiology , Humans , Immunohistochemistry , Lip Neoplasms/complications , Lip Neoplasms/pathology , Magnetic Resonance Imaging , Male , Middle Aged , Nerve Sheath Neoplasms/complications , Nerve Sheath Neoplasms/pathology , Parotid Gland/surgery , Parotid Neoplasms/complications , Parotid Neoplasms/pathology , Tomography, X-Ray Computed
20.
Otol Neurotol ; 26(3): 525-7, 2005 May.
Article En | MEDLINE | ID: mdl-15891661

OBJECTIVE: A vertebral artery aneurysm mimicking a contralateral cerebellopontine angle tumor is described. This is only the second reported case of this in the literature. STUDY DESIGN: Case report. SETTING: Radcliffe Infirmary, Oxford, United Kingdom. PATIENT: Seventy-year-old female patient who presented with a gradually deteriorating right-sided sensorineural hearing loss and a right facial palsy. INTERVENTIONS: Magnetic resonance imaging scan and computed tomography angiography with three-dimensional reconstruction followed-up by endovascular coiling of a vertebral artery aneurysm. MAIN OUTCOME MEASURE: Deterioration in neurologic status. RESULTS: Satisfactory recovery, and at 3 months, the patient is well with no deterioration in facial nerve function. CONCLUSION: Imaging by means of computed tomography angiography complements the standard magnetic resonance imaging scan in the rare event of an aneurysm at the cerebellopontine angle. Endovascular coiling occlusion is a recognized and effective way of managing intracranial aneurysms at the cerebellopontine angle.


Cerebellar Neoplasms/diagnosis , Cerebellopontine Angle , Intracranial Aneurysm/diagnosis , Vertebral Artery , Aged , Cerebral Angiography , Diagnosis, Differential , Embolization, Therapeutic/instrumentation , Embolization, Therapeutic/methods , Female , Humans , Image Processing, Computer-Assisted , Intracranial Aneurysm/therapy , Magnetic Resonance Imaging , Tomography, X-Ray Computed
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