Results 11 to 20 of about 1,037 (94)
Carotid cavernous fistula: A rare but treatable cause of ophthalmoplegia - A case report
Carotid cavernous fistulas (CCFs) are a rare but debilitating entity that may present with orbital or cerebral venous hypertension. CCFs may pose diagnostic and management pitfalls for clinicians as they can initially be misdiagnosed as primary orbital ...
Neeharika Krothapalli +5 more
doaj +1 more source
Background Tolosa-Hunt syndrome (THS) is characterized by painful ophthalmoplegia caused by idiopathic granulomatous inflammation involving the cavernous sinus region. Patients respond well to steroid therapy.
Wei He +5 more
doaj +1 more source
血管病相关性眼肌麻痹病因的研究进展 Study Progress of Etiology of Ophthalmoplegia Associated with Vascular Disease
眼肌麻痹是神经内科、眼科、神经眼科的常见体征。根据病变部位,血管病相关的眼肌 麻痹可分为核上型、核型、核间型、周围神经型,不同型别的眼肌麻痹有不同的病因。核上型、核型 及核间型眼肌麻痹多见于卒中,其中核型眼肌麻痹以动眼神经核受累最常见。周围神经型眼肌麻痹 病因众多,如糖尿病性眼肌麻痹、动脉瘤、颈内动脉海绵窦瘘等。糖尿病性眼肌麻痹多累及动眼神经, 瞳孔受累较轻,一般数周后开始恢复;动脉瘤和颈内动脉海绵窦瘘所致眼肌麻痹需行数字减影血管 造影(digital subraction angiography ...
李然,景筠
doaj +1 more source
Neurotoxin envenomation mimicking brain death in a child: A case report and review of literature
The spectrum of presentation of a victim of neurotoxic snake bite can range from mild ptosis to complete paralysis and ophthalmoplegia. We report a case of snake bite in a 10-year-old child who was comatosed with bilateral fixed dilated pupils and absent
Madhu Dayal +3 more
doaj +1 more source
Hypopituitarism secondary to a pituitary metastasis is rare and difficult to diagnose since its symptoms are nonspecific. The presence of visual deficits and nerve palsies should suggest the presence of a pituitary metastasis in a cancer patient.
Ibtissem Oueslati +5 more
doaj +1 more source
Surgery for Pituitary Tumor Apoplexy Is Associated with Rapid Headache and Cranial Nerve Improvement
Pituitary tumor apoplexy (PTA) classically comprises sudden-onset headache, loss of vision, ophthalmoparesis, and decreased consciousness. It typically results from hemorrhage and/or infarction within a pituitary adenoma.
Kevin A. Cross +13 more
doaj +1 more source
MYH2 myopathy, a new case expands the clinical and pathological spectrum of the recessive form
Background Hereditary myosin myopathies are a group of rare muscle disorders, caused by mutations in genes encoding for skeletal myosin heavy chains (MyHCs). MyHCIIa is encoded by MYH2 and is expressed in fast type 2A and 2B muscle fibers. MYH2 mutations
Roberta Telese +12 more
doaj +1 more source
Congenital fibrosis of the extraocular muscles
Background : Congenital fibrosis of the extraocular muscles (CFEOM) describes a group of rare congenital eye movement disorders that result from the dysfunction of all or part of the oculomotor (CN 3) and the trochlear (CN 4) nerves, and/or the muscles ...
Pascale Cooymans +3 more
doaj +1 more source
OHerpes Zoster Oftálmico (HZO) decorre da infecção pelo vírus da varicela-zoster que permanece latente no gânglio de Gasser até que seja reativado e comprometa a divisão oftálmica do nervo trigêmeo.
Kenzo Hokazono +3 more
doaj +1 more source
To wait for a spontaneous recovery of the third cranial nerve palsy occurring after the coiling of a PcomA aneurysm or to implement surgical treatment? A case report [PDF]
Introduction. In the last two decades a method of endovascular embolization has been imposed as a method of choice in the treatment of unruptured intracranial aneurysms.
Peulić Miodrag +3 more
doaj +1 more source

