Results 21 to 30 of about 466 (103)

Orbital Perivascular Epithelioid Cell Tumor in a Case of Tuberous Sclerosis

open access: yesCase Reports in Ophthalmology, 2023
The aim of the study was to report a case of orbital perivascular epithelioid cell tumor (PEComa) in a known diagnosed patient of tuberous sclerosis and retinal astrocytic hamartoma.
Shaikha H Aljneibi   +3 more
doaj   +1 more source

Silent sinus syndrome: An imploding antrum syndrome

open access: yesJournal of Indian Academy of Oral Medicine and Radiology, 2016
Silent sinus syndrome (SSS) is a rare entity that is associated with spontaneous, painless, unilateral enophthalmos and hypoglobus resulting from downward bowing of the orbital floor in the absence of any symptomatic sinonasal disease.
Sneha H Choudhary   +3 more
doaj   +1 more source

Combined Single-Step Procedure for Correction of Silent Sinus Syndrome

open access: yesCase Reports in Ophthalmology, 2019
Silent sinus syndrome (SSS) is a rare condition characterized by enophthalmos and hypoglobus that is generally not related to trauma or surgery. We present a 30-year-old man who noticed facial asymmetry during the previous month and was referred to our ...
Roee Arnon   +4 more
doaj   +1 more source

Orbital cholesterol granuloma: A report and discussion of orbital findings

open access: yesAmerican Journal of Ophthalmology Case Reports, 2019
Purpose: To report a case of orbital cholesterol granuloma and discuss the orbital findings seen in this entity. Observation: A 38-year-old male presented with an 8-month history of progressive left upper lid ptosis and hypoglobus.
Andrew J. Rong   +4 more
doaj   +1 more source

Natural progression of bilateral maxillary silent sinus syndrome: A metachronous case report

open access: yesSAGE Open Medical Case Reports, 2020
Silent sinus syndrome refers to a constellation of spontaneous and progressive enophthalmos and hypoglobus in the setting of asymptomatic ipsilateral maxillary sinus atelectasis.
Bianca Rullan-Oliver   +2 more
doaj   +1 more source

A deadly droop: small cell lung cancer presenting as upper eyelid ptosis

open access: yesVision Pan-America, 2014
Orbital metastases are a rare manifestation of systemic malignancies, most commonly originating from the breast or lung in adults. Not infrequently there is not any diagnosis of cancer at the time of presentation with orbital metastatic disease.
Son T. Ho, Alejandra A. Valenzuela
doaj   +1 more source

A Rare Pediatric Case of Lacrimal Gland Pleomorphic Adenoma

open access: yesPlastic and Reconstructive Surgery, Global Open, 2019
Summary:. Pleomorphic adenoma of the lacrimal gland is a rare benign finding in adults, and extremely uncommon in children. These tumors often present with increased propotosis or hypoglobus, and they invariably require operative excision.
Justin R. Bryant, DO, MBA   +6 more
doaj   +1 more source

Silent sinus syndrome

open access: yesTurkish Archives of Otorhinolaryngology, 2011
Ophthalmic complications due to sinus diseases are often seen and well known. But ophthalmic complications due to silent sinus syndrome are rare clinical entities.
Seçil Bahar Akyol   +2 more
doaj   +1 more source

A Case of Medialized Lateral Maxillary Sinus Wall: A Pillar of Support

open access: yesCase Reports in Medicine, Volume 2018, Issue 1, 2018., 2018
The number of maxillofacial trauma (MFT) cases attended in the Emergency Department is progressively increasing in trend, owing to the rising statistics of motor‐vehicle accidents (MVAs) and urban assaults in addition to occupational‐related injuries. Prompt and thorough assessment is important for accurate diagnosis and paramount treatment plans.
I. A. Othman   +3 more
wiley   +1 more source

Clinical and morphological features of the orbital floor in a patient with silent sinus syndrome: A clinical case report

open access: yesRussian Open Medical Journal
Silent sinus syndrome (SSS) is a rare condition characterized by spontaneous unilateral displacement of the inferior and posterior globe due to maxillary sinus (MS) atelectasis.
Vladimir A. Sheptulin   +2 more
doaj   +1 more source

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