نتایج جستجو برای: multiple cranial neuropathies

تعداد نتایج: 790101  

2011
Alan Siu Ameet Singh Fabio Roberti

Sinus mucoceles are benign, slowly enlarging, mucous-secreting, cystic lesions whose expansile growth may lead to compressive neuropathies. We present the case of a 70-year-old woman with a long-standing history of headaches and progressive ocular neuropathy who underwent an endoscopic resection of a large sphenoid sinus mucocele resulting in immediate improvement of her neurological symptoms. ...

Journal: :iranian journal of allergy, asthma and immunology 0
mohammad gharagozlou fariborz zieh parviz tabatabaei gholamreza zamani

there are few reports about congenital indifference to pain or hereditary and sensory autonomic neuropathy (hsan). several investigations for pathophysiology of this syndrome have been performed and different classifications about it. in this report we present a case of hsan type ii with general absence of pain and self amputations and leprosy–like damage of extremities which was suspected to b...

2010
Shiv Saidha Jennifer Spillane Gerard Mullins Brian McNamara

BACKGROUND We hypothesized that a wide range of surgical procedures may be complicated by neuropathies, not just in close proximity but also remote from procedural sites. The aim of this study was to classify post-operative neuropathies and the procedures associated with them. METHODS We retrospectively identified 66 patients diagnosed with post-procedure neuropathies between January 2005 and...

2016
Alexandra Lovett Tracey Cho

Sarcoidosis is a multisystemic granulomatous disease of unknown etiology. Neurological symptoms occur in 5-15% of patients with sarcoidosis and are related to a whole spectrum of possible pathologies, including pachymeningitis, leptomeningitis, parenchymal involvement with mass lesions and/or white matter disease, myelitis, cranial neuropathies, peripheral neuropathy, and myopathy. Diagnosis ca...

2018
Margaret L. Pfeiffer Helen A. Merritt Lucy A. Bailey Karina Richani Margaret E. Phillips

Purpose To describe a case of orbital apex syndrome as a result of isolated bacterial sinusitis. Observations A 63-year-old woman presented with an orbital apex syndrome from isolated bacterial sinusitis with rapidly declining visual acuity to no light perception. We compared our case with 6 similar cases of severe vision loss from isolated bacterial sinusitis. In contrast to previously publi...

Journal: :Head & neck 2015
Daniel W Flis Ameer T Shah Jeremiah C Tracy Carl B Heilman Miriam A O'Leary

BACKGROUND The differential diagnosis of skull base masses is diverse and includes benign and malignant neoplasms, vascular anomalies, congenital lesions, as well as infectious and inflammatory processes. Metastatic masses of the skull base are a rare manifestation of systemic malignancies. Breast cancer is the most common cause of skull base metastases. Villaret syndrome refers to cranial nerv...

2017
Yuya Kobayashi Yasufumi Kondo Kana Uchibori Jun Tsuyuzaki

Recurrent painful ophthalmoplegic neuropathy (RPON) is a rare condition that manifests as headache and ophthalmoplegia. It typically occurs in children. Although migraine or neuropathy have been suggested as etiologies, the precise etiology remains unclear. In the International Classification of Headache Disorders 3rd edition-beta version (ICHD3β) (code 13.9), RPON was categorized into painful ...

Journal: :Neuromuscular disorders : NMD 2005
E Mikesová K Hühne B Rautenstrauss R Mazanec L Baránková M Vyhnálek O Horácek P Seeman

Mutations in the early growth response 2 gene (EGR2) cause demyelinating neuropathies differing in severity and age of onset. We tested 46 unrelated Czech patients with dominant or sporadic demyelinating CMT neuropathy for mutations in the EGR2 gene. One novel de-novo mutation (Arg359Gln, R359Q) was identified in heterozygous state in a patient with a typical CMT1 phenotype, progressive moderat...

2014
Jeong-Hyun Byun Jong-Hoo Lee In-Sung Choi

Churg-Strauss syndrome (CSS) is a rare systemic necrotizing vasculitis. Cranial nerve involvement is very rare in CSS. A 59-year-old woman had complained of both hearing impairments for eight months and left facial palsy for three months. Left facial and cochlear neuropathies were detected in electrodiagnostic studies. Paranasal sinus computed tomography (CT) showed chronic pansinusitis. Chest ...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید