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Dive into the research topics where John K. Goudakos is active.

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Featured researches published by John K. Goudakos.


Clinical Otolaryngology | 2011

Endoscopic versus microscopic trans‐sphenoidal pituitary surgery: a systematic review and meta‐analysis

John K. Goudakos; Konstantinos Markou; C. Georgalas

Clin. Otolaryngol. 2011, 36, 212–220


Otology & Neurotology | 2010

Corticosteroids in the Treatment of Vestibular Neuritis: A Systematic Review and Meta-Analysis

John K. Goudakos; Konstantinos Markou; Valérie Franco-Vidal; Victor Vital; Miltiadis Tsaligopoulos; Vincent Darrouzet

Objective: To systematically review and meta-analyze the results of all randomized controlled trials comparing corticosteroids with placebo for the treatment of patients with vestibular neuritis. Data Sources: An electronic search was performed in MEDLINE, EMBASE, Cochrane Library, and CENTRAL databases, and then extensive hand-searching was performed for the identification of relevant studies. No time and language limitations were applied. Study Selection: Prospective randomized controlled trials comparing corticosteroids with placebo for the treatment of patients with vestibular neuritis. Data Extraction: Odds ratios (ORs), weighted mean differences (WMD), 95% confidence intervals (CIs), and tests for heterogeneity were reported. Data Synthesis: Four studies were eventually identified and systematically reviewed. Meta-analysis was feasible for 3 studies. Regarding the recovery of clinical symptoms, the proportion of patients with clinical recovery at 1 month after the initiation of therapy did not differ significantly between the corticosteroids and placebo groups (OR, 1.45; 95% CI, 0.26-8.01; p = 0.67). The proportion of patients with caloric complete recovery was significantly different between the corticosteroids and placebo groups both at 1 (OR, 12.64; 95% CI, 2.6-61.52; p = 0.002; heterogeneity, p = 0.53; fixed effects model) and 12 months (OR, 3.35; 95% CI, 1.45-7.76; p = 0.005; heterogeneity, p = 0.03; random effects model) after the initiation of therapy. The caloric extent of canal paresis at 12 months after the initiation of therapy seemed to differ significantly between patients who received corticosteroids and those who received placebo (WMD, −12.15; 95% CI, −19.85 to −4.46; p < 0.05; heterogeneity, p < 0.05; random effects model). Conclusion: The present systematic review and meta-analysis, based on the currently available evidence, suggests that corticosteroids improve only the caloric extent and recovery of canal paresis of patients with vestibular neuritis. At present, clinical recovery does not seem be better in patients receiving corticosteroids.


Head and Neck-journal for The Sciences and Specialties of The Head and Neck | 2009

PRIMARY LARYNGEAL LYMPHOMA: REPORT OF 3 CASES AND REVIEW OF THE LITERATURE

Konstantinos Markou; John K. Goudakos; J. Constantinidis; Ioannis Kostopoulos; Victor Vital; Angelos Nikolaou

Extranodal lymphomas limited to the larynx are rare, accounting for less than 1% of all laryngeal neoplasms. The aim of this study was to report the experience of our department in the management of these aggressive lesions, as they require special diagnostic and therapeutic attention.


European Archives of Oto-rhino-laryngology | 2009

An overview of the etiology of otosclerosis

Konstantinos Markou; John K. Goudakos

Otosclerosis is the primary disease affecting the homeostasis of otic capsule and is among the most common causes of acquired hearing loss. Otosclerosis is considered as a multifactor disease, caused by both genetic and environmental factors. The aim of the present review is to summarize and analyze the bibliographic data, associated with the etiology of the disease. In some cases, the otosclerosis has an autosomal dominant mode of inheritance with incomplete penetrance. Genetic studies reveal the occurrence of at least nine chromosomal loci as candidate genes of the disease. The localized measles virus infection of the otic capsule has been postulated as a possible etiological theory. The role of hormonal factors, immune and bone-remodeling system in the etiopathogenesis of otosclerosis and the association of the disease with the disorders of the connective tissue are the issues of the present study. Despite the extensive research, many etiological factors and theories have been suggested and the process of development of the otosclerosis remains unclear.


Otolaryngologic Clinics of North America | 2011

Osteoma of the Skull Base and Sinuses

Christos Georgalas; John K. Goudakos; Wytske J. Fokkens

Osteomata of the frontal and ethmoid sinuses have traditionally been surgically removed via external approaches. However, endoscopic techniques have increasingly been used for the surgical management of selected cases. Advances in visualization and instrumentation, as well as the excellent access provided by the Draf type 3 procedure, expanded the reach of endoscopes. We describe current limits of endoscopic approaches in the removal of osteomata from the frontal sinus and our algorithms for their management. We believe that the vast majority of frontal sinus osteomata can be managed endoscopically, and that only significant anterior or extreme infero-lateral extension constitute major limiting factors.


American Journal of Otolaryngology | 2012

Unique case of malignant transformation of a vestibular schwannoma after fractionated radiotherapy.

Konstantinos Markou; Sandrine Eimer; Clotilde Perret; Aymeri Huchet; John K. Goudakos; Dominique Liguoro; Valérie Franco-Vidal; Jean-Philippe Maire; Vincent Darrouzet

OBJECTIVE Malignant transformation of vestibular schwannoma is considered a rare clinical entity. Radiotherapy, as a treatment option for vestibular schwannoma, is regarded as a potential risk factor for secondary malignancy. Recently, radiotherapy with dose fractionation has been proposed, intended to diminish the risk of radiation-induced neuropathy. CASE PRESENTATION The aim of the present study is to report the first case, to the best of our knowledge, of malignant transformation of a residual vestibular schwannoma 19 years after fractionated radiotherapy, describing its characteristics with regard to those previously reported in the literature. CONCLUSIONS The main purpose of the present work is to state that the knowledge of the iatrogenic potential pitfalls of any technique of radiotherapy in clinical oncology is becoming a necessity. Finally, our report demonstrates that the irradiated patients must be monitored for life because a secondary malignancy may appear after a very long delay.


Archives of Medical Science | 2012

Association between primary nocturnal enuresis and habitual snoring in children with obstructive sleep apnoea-hypopnoea syndrome.

Afroditi Sakellaropoulou; Maria Hatzistilianou; Maria Emporiadou; Victor Aivazis; John K. Goudakos; Konstantinos Markou; Fanni Athanasiadou-Piperopoulou

Introduction Nocturnal enuresis (NE) and obstructive sleep apnoea-hypopnoea syndrome (OSAHS) are common problems during childhood, and population studies have reported a significant correlation between them. This study aimed to assess whether habitual snoring, mouth breathing and daytime sleepiness are associated with increased incidence of NE in children with OSAHS. Material and methods Polysomnography was performed in 42 children (66.7% males), 3.5-14.5 years old, who were evaluated for sleep-disordered breathing (SDB). Results Fourteen out of 42 children (33.3%) presented mild, 16 out of 42 (38.1%) moderate and 12 out of 42 (28.6%) severe degree of OSAHS. Apnea hypopnea index (AHI) ranged between 1.30-94.20 (10.54 ±15.67) events per hour of sleep. Nocturnal enuresis was reported in 7/42 (16.7%) of them. The main observed symptoms were snoring (90.5%), restless sleep (81%), mouth breathing (71.4%), nasal congestion (76.2%), and difficulty in arousal (52.4%). A statistically significant association was found between NE and mouth breathing (p = 0.014) or nasal congestion (p = 0.005). Children with OSAHS and NE had a higher arousal index (8.14 ±8.05) compared with OSAHS children without NE (4.61 ±7.95) (p = 0.19, z = –1.28). Snorers had higher levels of AHI (11.02 ±16.37) compared with non-snorers (6.05 ±4.81) (p = 0.33, z = –0.96), and habitually snorers (23/42, 54.76%) were at greater risk of having NE (4/23) than were non-snorers (0/4, p = 0.36). However, the prevalence of enuresis was not related to the severity of OSAHS, expressed as AHI (p = 0.70). Conclusions Mouth breathing, nasal congestion and high threshold of arousal during sleep should be more carefully evaluated in cases of children with NE who do not respond to standard treatment and present SDB.


American Journal of Otolaryngology | 2013

Sarcoidosis-like granulomatosis of the hypopharynx as a complication of anti-TNF therapy.

Artemis Christoforidou; John K. Goudakos; Mattheos Bobos; Efthimios Lefkaditis; Victor Vital; Konstantinos Markou

INTRODUCTION Sarcoidosis is a multisystem granulomatous disease of unknown etiology, occasionally presenting with signs and symptoms that occur within the head and neck. Recently, granulomatous reactions and cases of sarcoidosis have been reported in patients treated with anti-TNF agents. METHODS This report describes a 56-year-old man who developed sarcoidosis in the hypopharynx during adalimumab therapy for psoriatic arthritis. A retrospective review of the literature was performed using the PubMed database. RESULTS In our patient, a chronic granulomatous reaction consistent with sarcoidosis developed after 2 years of continuous treatment with adalimumab. The diagnosis of sarcoidosis was established by the typical well-formed non caseating granulomas on biopsy, after excluding all other granulomatous conditions. Following withdrawal of anti-TNF agents and a course of steroids, the clinical picture resolved. CONCLUSIONS The development of sarcoidosis during treatment with TNF-a antagonists represents a rare and paradoxical adverse event. To our knowledge this is the first case of sarcoidosis of the hypopharynx reported in the literature.


Case reports in otolaryngology | 2013

Hybrid Carcinoma of the Larynx: A Case Report (Adenoid Cystic and Adenocarcinoma) and Review of the Literature

Ilias Karasmanis; John K. Goudakos; Vital I; Thomas Zarampoukas; Victor Vital; Konstantinos Markou

Introduction. The nonsquamous carcinomas of the larynx are considered rare with the majority of malignant tumors in this area, reaching the rate of 95%, to be squamous cell neoplasms. Case Report. The case refers to a 53-year-old man that presented with symptomatology of motor nerve disease. During the evaluation of the neurologic disease, a subglottic mass of the larynx was revealed accidentally in the imaging examination. Under general anesthesia, we performed direct laryngoscopy and biopsy of the mass. The histopathologic examination revealed a hybrid carcinoma coexistence of two different carcinomas, an adenoid cystic carcinoma and an adenocarcinoma, not otherwise specified with poor differentiation. Regarding the therapeutic plan, the mass was considered inoperable due to its expansion to trachea and the patient received radiotherapy. Conclusions. Both the adenocarcinoma and adenoid cystic carcinoma are extremely rare types of malignant tumors in the larynx. The special interest of the present case is the coexistence of these two rare tumors in the same region of the larynx, being a hybrid tumor of the salivary glands in the larynx, which is the second reported case, based on our systematic literature review.


Acta Neurochirurgica | 2013

Lipochoristomas of the cerebellopontine angle and internal acoustic meatus: a seven-case review.

Konstantinos Markou; John K. Goudakos; Olivier Bellec; Dominique Liguoro; V. Franco-Vidal; Christian Rattin; Vincent Darrouzet

BackgroundIntracranial lipomas are extremely rare tumors, with certain clinical and radiological characteristics.MethodsWe considered the diagnostic evaluation and treatment options of seven patients presenting with lipoma in the cerebellopontine angle or internal acoustic meatus in our department.ResultsMean age was 51, with four out of seven cases being women. Balance disorders (vertigo, dizziness) were the predominant symptoms (in six out of seven patients), followed by hearing loss. The diagnosis of intracranial lipomas was based on the results of imaging studies, especially on magnetic resonance imaging. The management of lipomas of the CPA and of the IAM should initially be conservative, including close follow-up of the patient and evaluation of a potential change in tumor size. Surgical management of CPA lipomas should be reserved for patients with intractable clinical symptoms due to tumor overgrowth.ConclusionsDiagnosis of CPA and IAM lipomas is considered to be a clinical and imaging challenge. As the complete resection of such lipomas is a risky choice and taking into account the benign course of such tumors, the only absolute surgical indication should be uncontrolled tumor growth.

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Konstantinos Markou

Aristotle University of Thessaloniki

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Victor Vital

Aristotle University of Thessaloniki

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Angelos Nikolaou

Aristotle University of Thessaloniki

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Vincent Darrouzet

Université Bordeaux Segalen

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George Psillas

Aristotle University of Thessaloniki

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Ilias Karasmanis

Aristotle University of Thessaloniki

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Stefanos Triaridis

Aristotle University of Thessaloniki

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Miltiadis Tsaligopoulos

Aristotle University of Thessaloniki

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Sarantis Blioskas

Aristotle University of Thessaloniki

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