Results 41 to 50 of about 4,416 (194)

Pituitary metastasis of breast cancer mimicking IgG4-related hypophysitis

open access: yeseNeurologicalSci, 2019
IgG4-related hypophysitis, which is the pituitary gland inflammation caused by IgG4 positive lymphocytes, can affect cavernous sinus and orbital apex leading to developing cranial nerve related symptoms such as orbital apex syndrome (OAS). Here we report
Kanako Nose   +5 more
doaj   +1 more source

Total remission of Tolosa-Hunt Syndrome with single-dose of infliximab [PDF]

open access: yesRevista Brasileira de Oftalmologia, 2020
Tolosa-Hunt syndrome is a painful ophthalmoplegia caused by non-specific granulomatous inflammation, corticoid-sensitive, of the cavernous sinus. The etiology is unknown. Recurrences are common.
Luís Armando Vitorino Alves de Souza Gondim   +4 more
doaj   +1 more source

Orbital apex syndrome secondary to a fungal nasal septal abscess caused by Scedosporium apiospermum in a patient with uncontrolled diabetes: a case report

open access: yesBMC Infectious Diseases, 2017
Background Orbital apex syndrome is a localized type of orbital cellulitis, where mass lesions occur at the apex of the cranial nerves. Although nasal septal abscess is uncommon, the organism most likely to cause nasal septal abscess is Staphylococcus ...
Ippei Kishimoto   +5 more
doaj   +1 more source

Azathioprine in orbital apex syndrome

open access: yesIndian Journal of Pharmacy and Pharmacology, 2020
Orbital Apex Syndrome (OAS) is commonly caused by specific inflammations, infections, neoplasms, iatrogenic, trauma, vascular and non-specific orbital inflammation (NSOI). OAS secondary to NSOI responds rapidly to corticosteroids. There are very few case reports on azathioprine as additional treatment modality in OAS secondary to NSOI.
Saptagirish Rambhatla, Neha Arora
openaire   +2 more sources

Outcomes in Orbit‐Sparing Versus Orbit‐Sacrificing Surgery for Sinonasal Malignancies With Orbital Involvement: A Systematic Review and Meta‐Analysis

open access: yesWorld Journal of Otorhinolaryngology - Head and Neck Surgery, EarlyView.
ABSTRACT Background Sinonasal malignancies with orbital involvement may be managed with orbit‐sacrificing or orbit‐preserving surgical approaches, with a recent shift towards orbital preservation to reduce postoperative morbidity while maintaining oncological success.
Claire Jing‐Wen Tan   +9 more
wiley   +1 more source

Curious case of a frozen pupil – Orbital apex syndrome

open access: yesJEM Reports
Background: Orbital apex syndrome is a rare neurological disorder that occurs due to damage of cranial nerves at the apex of the orbit. Differentiating it from other ocular syndromes can be diagnostically challenging.
Sophia Aguirre, Rahul Nene
doaj   +1 more source

Orbital Apex Syndrome Secondary to Herpes Zoster Ophthalmicus

open access: yes, 2023
A rare complication of Herpes Zoster Ophthalmicus is orbital apex syndrome characterized by optic neuropathy, ophthalmoplegia and ptosis.
Evan Jameyfield; Peter MacIntosh; Ann-Marie Lobo-Chan
core  

Prelacrimal Transmaxillary‐Orbital Approach for Resection of Lateral Extraconal Orbital Cavernous Hemangioma

open access: yesWorld Journal of Otorhinolaryngology - Head and Neck Surgery, EarlyView.
ABSTRACT Endoscopic orbital surgery is likely a reasonable option for patients with orbital cavernous hemangiomas (OCH) medial to the optic nerve (ON). The endoscopic resection of OCH lateral to the ON is extremely challenging. Zhou et al. first described the endoscopic prelacrimal recess approach (PLRA) for the management of the maxillary sinus and ...
Zhen‐Xiao Huang   +2 more
wiley   +1 more source

Invasive Fungal Rhinosinusitis with Orbital Apex Syndrome Leading to Brain Abscess in a Patient with Ulcerative Colitis [PDF]

open access: yes
We report the case of a 65-year-old male who presented with a 1-week history of right periorbital pain and progressive visual loss. He had a history of ulcerative colitis and was taking oral corticosteroids and mesalazine.
藤原, 和典   +30 more
core   +1 more source

International Guideline on the Diagnosis and Management of Pediatric Patients With Hereditary Angioedema

open access: yesAllergy, EarlyView.
ABSTRACT Hereditary angioedema (HAE) with C1 inhibitor deficiency is a rare disease characterized by unpredictable episodes of tissue swelling (angioedema), which, in most cases, occur first under the age of 18 years, and entail a significant burden of disease not only for the patients but also for their families.
Henriette Farkas   +128 more
wiley   +1 more source

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