keyword
https://read.qxmd.com/read/35932634/the-diagnostic-signature-of-susac-s-syndrome
#21
JOURNAL ARTICLE
Todd A Hardy
No abstract text is available yet for this article.
August 3, 2022: Journal of Clinical Neuroscience: Official Journal of the Neurosurgical Society of Australasia
https://read.qxmd.com/read/35620189/auricular-erythermalgia-showing-excellent-response-to-itraconazole-a-case-report
#22
Yan-Ting Ye, Jing-Fa Lu, Hui-Hui Wu, Juan-Hua Liu, Yu-Kun Zhao, Di-Qing Luo
Erythermalgia, a rare painful disorder, is characterized by recurrent pain attacking, warmth, and erythema that mainly involves the distal extremities. Red ear syndrome shares similar clinical features of erythermalgia afflicting the external ear with unilateral/bilateral distribution. The treatments of both diseases are still difficult without controlled therapeutics available up to date. A 12-year-old boy was referred because of 3 years of recurrent attacking of painful erythema and warmth that involved the ears alone, the episodes occurred several times daily with duration of dozens of minutes to hours for each flare...
2022: Therapeutic Advances in Chronic Disease
https://read.qxmd.com/read/35510338/if-your-ears-are-burning-we-must-be-talking-about-red-ear-syndrome-a-brief-report
#23
JOURNAL ARTICLE
Ashling Courtney, Zack Holmes, Stephanie Weston
Red Ear Syndrome is an uncommon disorder that can affect all age groups. It is frequently referred to Dermatology as it can present similarly to erythromelalgia. Although the exact pathophysiology is unknown, a common hypothesis suggests a shared pathophysiological background with migraine due to their well-known association. Currently, there are no established treatment guidelines. Delays in accurate diagnosis and commencing optimal treatment can significantly negatively impact on a patients quality of life...
August 2022: Australasian Journal of Dermatology
https://read.qxmd.com/read/35310317/idiopathic-red-ear-syndrome-a-rare-case-report
#24
Brihaspati Sigdel, Amrit Pokhrel
Red ear syndrome (RES) is a very rare disorder that is characterized by a unilateral or bilateral attack of paroxysmal burning sensation and reddening of the external ear. The duration of symptoms ranges from a few seconds to hours. It can occur spontaneously or be triggered by rubbing of the ear, heat or cold stimulation, brushing of hair, and neck movement. Diagnosis and treatment of this condition are challenging. The pathophysiology of RES is still unclear and hypotheses involving peripheral or central nervous system mechanisms have been proposed...
March 2022: Clinical Case Reports
https://read.qxmd.com/read/35045844/inflammation-and-necrosis-syndrome-is-associated-with-alterations-in-blood-and-metabolism-in-pigs
#25
JOURNAL ARTICLE
Frederik Loewenstein, Sabrina Becker, Josef Kuehling, Hansjörg Schrade, Mirjam Lechner, Robert Ringseis, Klaus Eder, Andreas Moritz, Gerald Reiner
BACKGROUND: Swine inflammation and necrosis syndrome (SINS) can lead to significant clinical alterations at tail, ears, claws and other parts of the body in suckling piglets, weaners and fatteners. Clinical findings are associated with vasculitis, intima proliferation and thrombosis. The syndrome can be found in newborns, indicating a primarily endogenous aetiology. It has been hypothesized that SINS is triggered by gut-derived microbial-associated molecular patterns, causing derangements in liver metabolism and activity of peripheral white blood cells involving inflammation and blood haemostasis...
January 19, 2022: BMC Veterinary Research
https://read.qxmd.com/read/35039289/telehealth-voice-assessment-by-speech-language-pathologists-during-a-global-pandemic-using-principles-of-a-primary-contact-model-an-observational-cohort-study-protocol
#26
JOURNAL ARTICLE
Christopher L Payten, Duy Duong Nguyen, Daniel Novakovic, John O'Neill, Antonia M Chacon, Kelly A Weir, Catherine J Madill
INTRODUCTION: SARS-CoV-2, a highly contagious severe acute respiratory syndrome, has spread to most countries in the world and resulted in a change to practice patterns for the assessment and diagnosis of people with voice disorders. Many services are transitioning to telehealth models to maintain physical distancing measures and conserve personal protective equipment used by healthcare workers during laryngoscopy examinations. The speech-language pathology primary contact (SLPPC) assessment for patients referred to ear, nose and throat (ENT) services in Australia has been shown to reduce waiting times for assessment while streamlining access to ENT assessment and allied health practitioner treatment pathways...
January 17, 2022: BMJ Open
https://read.qxmd.com/read/35022354/a-rare-case-of-ankylosing-spondylitis-coexisting-with-relapsing-polychondritis-antiphospholipid-syndrome-and-myelodysplastic-syndrome
#27
JOURNAL ARTICLE
Hanna Park, Jung Gon Kim, Wan-Uk Kim
Ankylosing spondylitis (AS) is rarely accompanied by other autoimmune diseases and/or hematologic disorders. We herein report a 46-year-old man with AS coexisting with relapsing polychondritis (RP), antiphospholipid syndrome (APS) and myelodysplastic syndrome (MDS). While receiving anti-TNF therapy for AS, the patient developed anemia and was diagnosed with MDS. After six months, he developed swelling and redness of the nose and both auricles. RP was diagnosed by an ear biopsy. Afterward, during the evaluation of a repeated fever, APS was diagnosed...
January 13, 2022: Internal Medicine
https://read.qxmd.com/read/34881125/natural-killer-cell-deficiency-in-neuroblastoma-amplified-sequence-gene-mutation
#28
Rawia F Albar, Enad F Alsulimani, Khalid A Alsalmi, Abdulrahman Alnamlah, Abdullah Alhuzali, Saif Aljehani
Natural killer cell deficiency (NKD) occurs when decreased levels of such cells lead to major immunological deficiency in the patient. NK cells participate in tumor cell surveillance, viral infections, and immunoregulation in the body. We report a case of a nine-year-old female child, a known case of neuroblastoma amplified sequence (NBAS) gene mutation in the variant c.2819A>C (p. His940Pro), which causes infantile liver failure syndrome type 2 (ILFS2). The patient had been treated at four years of age for a three-day history of vesicular skin rashes in the L2 dermatome of the left leg, with pain and without swelling or redness, ear discharge, low appetite, and decreased activity...
November 2021: Curēus
https://read.qxmd.com/read/34873689/circadian-rhythmicity-on-red-ear-syndrome-in-a-patient-with-migraine-a-case-report
#29
JOURNAL ARTICLE
Americo Danúzio Pereira Oliveira, Raimundo Pereira Silva-Néto
BACKGROUND: Red ear syndrome (RES) was first described by Lance in 1994. It is characterized by recurrent attacks of redness of the ear, accompanied by burning pain, increased temperature, dysesthesia, and nosological relationship with headache. CASE: We report the case of a 43-year-old woman with migraine who developed RES. Redness episodes occurred at the same time of the day. She had a good therapeutic response to gabapentin. CONCLUSIONS: To the best of our knowledge, this is the first case of RES in which redness episodes occurred at the same time of the day...
December 7, 2021: Headache
https://read.qxmd.com/read/34868694/coexistence-of-relapsing-polychondritis-and-sickle-cell-disease-in-a-child
#30
Bernard Ofoe Tetteh, Florence-Barbara Yebuah, Maame-Boatemaa Amissah-Arthur, Dzifa Dey
Relapsing polychondritis (RP) is a rare, severe connective tissue disease of unknown etiology affecting cartilaginous and proteoglycan-rich structures in an episodic and inflammatory manner. Approximately a third of RP cases occur in conjunction with another disease usually systemic autoimmune rheumatic disease, or myelodysplastic syndrome. Sickle cell disease (SCD) is a common inherited hematologic condition characterized by the inheritance of two abnormal hemoglobins, of which one is a hemoglobin S, presenting with severe acute and chronic complications from vaso-occlusive phenomena, which can be difficult to differentiate from RP...
2021: Case Reports in Rheumatology
https://read.qxmd.com/read/34853046/paralysis-from-an-ear-infection-a-severe-case-of-otitis-externa-leading-to-acute-complete-cervical-cord-syndrome
#31
JOURNAL ARTICLE
Rachael Collins, George Lafford, Laura Parry
We report a case of a generally fit and well 54-year-old man who presented with a 2-day history of worsening left-sided otorrhea, headache, neck stiffness, vomiting and fever on the background of a 7-week history of otitis externa (OE). His condition progressed dramatically as he developed symptoms consistent with acute complete cervical cord syndrome with radiological evidence of skull base osteomyelitis, parapharyngeal, retropharyngeal and paravertebral abscesses and sigmoid sinus thrombus. Ultimately, he made a significant, although not complete, recovery...
December 1, 2021: BMJ Case Reports
https://read.qxmd.com/read/34786517/neurotrophic-corneal-ulcer-and-iridocyclitis-directly-preceding-ramsay-hunt-syndrome
#32
Farzan M Gorgani, Todd L Beyer
PURPOSE: To present to and inform the practitioner of an unusual presentation of Varicella zoster virus and Ramsay-Hunt Syndrome. OBSERVATIONS: A 69-year-old bedbound male with vascular dementia presented to the emergency room with a red right eye with associated tearing and mucus production. The patient could not express if he was in pain. The initial diagnosis from the emergency room was bacterial keratitis, confirmed with a positive pseudomonas culture. However, upon examination by the ophthalmologist it was noted that there was not only a large, infected epithelial defect, but also an intraocular pressure of 35 and a candy-cane hypopyon...
December 2021: American Journal of Ophthalmology Case Reports
https://read.qxmd.com/read/34674783/red-ear-syndrome-presenting-with-vestibular-migraine-case-study-and-review-of-the-literature
#33
REVIEW
S Kaneda, F Goto, T Teramura, K Okami
BACKGROUND: Red ear syndrome is a rare disorder in which the colour of the ear suddenly becomes red, with discomfort, pain and a burning sensation. This paper reports a case of primary red ear syndrome presenting with vestibular migraine. CASE REPORT: A 39-year-old woman from Bangladesh reported dizziness and repeated headaches experienced since 18 years of age. She initially attended our hospital with dizziness aged 34 years. When dizzy, the colour of her right ear sometimes became red...
December 2022: Journal of Laryngology and Otology
https://read.qxmd.com/read/34594512/long-term-changes-in-occurrence-relative-abundance-and-reproductive-fitness-of-bat-species-in-relation-to-arrival-of-white-nose-syndrome-in-west-virginia-usa
#34
JOURNAL ARTICLE
Catherine Johnson, Donald J Brown, Chris Sanders, Craig W Stihler
White-nose syndrome (WNS) is a disease caused by the fungus  Pseudogymnoascus destructans  which has resulted in the deaths of millions of bats across eastern North America. To date, hibernacula counts have been the predominant means of tracking the spread and impact of this disease on bat populations. However, an understanding of the impacts of WNS on demographic parameters outside the winter season is critical to conservation and recovery of bat populations impacted by this disease. We used long-term monitoring data to examine WNS-related impacts to summer populations in West Virginia, where WNS has been documented since 2009...
September 2021: Ecology and Evolution
https://read.qxmd.com/read/34352900/rare-disorders-of-the-vestibular-labyrinth-of-zebras-chameleons-and-wolves-in-sheep-s-clothing
#35
REVIEW
Julia Dlugaiczyk
The differential diagnosis of vertigo syndromes is a challenging issue, as many - and in particular - rare disorders of the vestibular labyrinth can hide behind the very common symptoms of "vertigo" and "dizziness". The following article presents an overview of those rare disorders of the balance organ that are of special interest for the otorhinolaryngologist dealing with vertigo disorders. For a better orientation, these disorders are categorized as acute (AVS), episodic (EVS) and chronic vestibular syndromes (CVS) according to their clinical presentation...
April 2021: Laryngo- Rhino- Otologie
https://read.qxmd.com/read/33623284/red-ear-syndrome-case-series-and-review-of-a-less-recognized-headache-disorder
#36
JOURNAL ARTICLE
Ishani Patel, Devangi Desai, Soaham Desai
No abstract text is available yet for this article.
September 2020: Annals of Indian Academy of Neurology
https://read.qxmd.com/read/33509289/the-effects-of-boar-on-susceptibility-to-swine-inflammation-and-necrosis-syndrome-in-piglets
#37
JOURNAL ARTICLE
Josef Kuehling, Kathrin Eisenhofer, Mirjam Lechner, Sabrina Becker, Hermann Willems, Gerald Reiner
Inflammation and necrosis can appear in pigs in several parts of the body simultaneously. The signs can affect newborns, suckling piglets and older pigs, and recent studies suggest that the syndrome is primarily endogenous. Inflammation and necrosis indicate impaired animal welfare, and thus should be controlled in pig production. This can be achieved by improving husbandry conditions. However, the variation in signs also appears to have a genetic component. The aim of the present study was therefore to test the effects of different boars from the Duroc and Pietrain breeds on the prevalence of swine inflammation and necrosis syndrome in their offspring...
January 28, 2021: Porcine Health Management
https://read.qxmd.com/read/33440309/red-ear-syndrome-in-children-review-of-literature-and-report-of-three-cases
#38
REVIEW
Antonina D'Amico, Cristina Galati, Maria Laura Manzo, Federica Reina, Giovanna Martina Nocera, Vincenzo Raieli
BACKGROUND: Red ear syndrome (RES) is a neurological syndrome that is characterized by attacks of redness and pain that is localized in the earlobe, accompanied by a burning sensation, swelling or otalgia. The exact pathophysiology of RES is not known. Several pediatric cases have been described. They show an extreme variability in clinical presentation and therapeutic response, and therefore there are numerous difficulties in the diagnostic-therapeutic approach and in the comprehension of the physiopathology...
March 2021: International Journal of Pediatric Otorhinolaryngology
https://read.qxmd.com/read/33063524/dental-and-craniofacial-characteristics-in-patients-with-14q22-1-q22-2-deletion-a-case-series
#39
JOURNAL ARTICLE
Marie Anne Roelandt, Koenraad Devriendt, Maria Cadenas de Llano-Pérula, Margot Raes, Guy Willems, Anna Verdonck
This case series is a follow-up report focusing on dental and facial characteristics in patients with a rare microdeletion in chromosome 14q22.1-q22.2. Usually, these patients have severe ocular, brain, and digital abnormalities. However, this case series shows that clinical presentation can be mild. Four relatives spanning 3 generations were diagnosed with a familial autosomal dominant 2.79 Mb microdeletion in chromosome 14q22.1-q22.2. Genetic screening was done by the Bacterial Artificial Chromosome array-comparative genome hybridization and was confirmed by the fluorescence in situ hybridization technique...
April 2021: Cleft Palate-craniofacial Journal
https://read.qxmd.com/read/32853394/red-ear-syndrome-after-tympanoplasty-a-new-association-to-add-to-the-list
#40
JOURNAL ARTICLE
Carolina Soares, Filipe Alves, Madalena Pinto, Pedro Abreu, Andreia Costa
No abstract text is available yet for this article.
October 2020: Headache
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