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Artykuły w czasopismach na temat "Retroorbital pain"

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Demir, Berat, Ghazi Abuzaid, Zeynep Ergenc, and Eda Kepenekli. "Delayed diagnosed Gradenigo’s syndrome associated with acute otitis media." SAGE Open Medical Case Reports 8 (January 2020): 2050313X2096611. http://dx.doi.org/10.1177/2050313x20966119.

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Gradenigo’s syndrome presents as a triad of retroorbital pain, ipsilateral abducens palsy, and purulent otorrhea. If the otologic pathologies in Gradenigo’s syndrome go unnoticed, the condition could be misdiagnosed with neurological diseases because of retroorbital pain and abducens palsy. Treatment of Gradenigo’s syndrome remains controversial. Although some reports state that long-term antibiotic treatment is sufficient, we recommended that management ought to be guided on a case-by-case basis depending on patient and disease factors. Herein, we report a delayed diagnosed pediatric case of
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Arustamyan, I. G., S. A. Karpischenko, O. A. Stancheva, et al. "Retrobulbar pain in isolated sphenoiditis." Meditsinskiy sovet = Medical Council, no. 7 (May 24, 2025): 150–55. https://doi.org/10.21518/ms2025-048.

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Introduction. The opacification of the unilateral sphenoidal sinus (USS) in computed tomography is caused by various diseases, including inflammation and infectious sinusitis, benign and malignant tumors and encephalocles. Symptoms of isolated lesions of this sinus are varied and nonspecific. This symptom includes retrobulbar pain, which does not occur with other paranasal spasms. This makes this symptom diagnostically valuable.Aim. Тo consider the relationship between the presence of retrobulbar pain in patients with isolated sphenoiditis and the nature of pathological changes in the sinus.Ma
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Foerderreuther, S., R. v. Maydell, and A. Straube. "A CPH-Like Picture in Two Patients with an Orbitocavernous Sinus Syndrome." Cephalalgia 17, no. 5 (1997): 608–11. http://dx.doi.org/10.1046/j.1468-2982.1997.1705608.x.

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Two patients with retroorbital pain syndromes with or without paresis of cranial nerves developed weeks after ipsilateral headache resembling chronic paroxysmal hemicrania (CPH) but without autonomic features. These findings might support the hypothesis that CPH may be caused by a pathological process in the region of the cavernous sinus, as has been proposed for the Tolosa-Hunt syndrome (THS).
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Viana, Pedro F., Harumoto Hasegawa, Josef Jarosz, Ata Siddiqui, Richard P. Selway, and Nandini Mullatti. "Short-lasting retroorbital pain attacks as a form of ictal epileptic headache: Case report." Cephalalgia 39, no. 9 (2019): 1195–99. http://dx.doi.org/10.1177/0333102419839792.

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Background and objectives Ictal epileptic headache is a rare form of painful seizure, habitually consisting of migrainous or tension-type headache. We describe a case of a patient with short-lasting, severe retroorbital pain attacks caused by frontal lobe epilepsy. Case report A 25-year-old male patient presented with recurrent attacks of paroxysmal, short-lasting, excruciating left periorbital and facial pain mainly occurring from sleep. After intracranial EEG exploration and resection of a right prefrontal focal cortical dysplasia, long-term seizure and headache remission was obtained. Discu
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Elashaal, AA, and Y. Elashaal. "P.138 Sphenoidal Sinus aspergillus infection presenting with right-sided painful ophthalmoplegia and cavernous sinus-orbital apex lesion: a case report." Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 50, s2 (2023): S93—S94. http://dx.doi.org/10.1017/cjn.2023.226.

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Background: Cavernous sinus-orbital apex aspergillosis is a rare but serious complication and difficult to diagnose based on clinical and radiological results. This condition is frequently diagnosed at a late stage because of its nonspecific and varying symptomatology, specifically in immuno-supressive patients. Early diagnosis and treatment is the key to prevent more serious central nerves system complications. Methods: We report the case of a 80-year-old man with a 2 month history of retroorbital pain before he developed a subacute cavernous sinus syndrome, with 3th cranial nerve palsy and r
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Peddi, Prakash, Kevin M. Gallagher, Chandrikha Chandrasekharan, et al. "Tolosa-Hunt Syndrome in Double-Hit Lymphoma." Case Reports in Oncological Medicine 2015 (2015): 1–4. http://dx.doi.org/10.1155/2015/249891.

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Tolosa-Hunt syndrome (THS) is a painful condition characterized by hemicranial pain, retroorbital pain, loss of vision, oculomotor nerve paralysis, and sensory loss in distribution of ophthalmic and maxillary division of trigeminal nerve. Lymphomas rarely involve cavernous sinus and simulate Tolosa-Hunt syndrome. Here we present a first case of double-hit B cell lymphoma (DHL) relapsing and masquerading as Tolosa-Hunt syndrome. The neurological findings were explained by a lymphomatous infiltration of the right Gasserian ganglion which preceded systemic relapse. As part of this report, the dia
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Bansal, Priyanshu, Vineet Sehgal, Lucky Bhalla, and Shaifali Arora. "Covid-19 induced optic neuritis – A case report." IP Indian Journal of Neurosciences 7, no. 4 (2022): 337–40. http://dx.doi.org/10.18231/j.ijn.2021.062.

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COVID-19 illness is an evolving disorder, and many extrapulmonary manifestations have been reported. With this report, we are highlighting one of the neuro-ophthalmologic complications of Covid-19. We report a case of 16 years old boy who presented with complaints of rapid loss of vision and retroorbital pain in the Right eye during recovery from Covid -19 infection. Clinically, radiologically, CSF, Blood, and all other investigations suggest Probable Covid -19 Right Eye Optic Neuritis. The patient showed remarkable recovery following steroid therapy. This report aims to add a case to the limi
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Maksimova, M. Yu, S. N. Illarioshkin, and I. A. Savizkaya. "Reccurent painful ophthalmoplegic neuropathy." Russian neurological journal 27, no. 6 (2023): 77–83. http://dx.doi.org/10.30629/2658-7947-2022-27-6-77-83.

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Reccurent painful ophthalmoplegic neuropathy (the Tolosa–Hunt syndrome) occurs due to a nonspecific granulomatous infl ammation of the walls of the cavernous sinus and the intracavernous segment of the internal carotid artery. It consists of one or more oculomotor nerves dysfunction associated with peri- and retroorbital pain; spontaneous remissions and relapses are typical. Oculomotor nerve disorders may coincide with the onset of pain or follow it within a period of up to 2 weeks. Demonstration of granulomatosis in the walls of the cavernous sinus and the intracavernous segment of the intern
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Vipassana V.Khandait, Vipassana V. Khandait, Sucheta S. Pawar Sucheta S. Pawar, Shreya A. Kirdat Shreya A.Kirdat, Akshata R. Sathe Akshata R. Sathe, and Pratiksha S. Khamkar Pratiksha S. Khamkar. "Unmasking Dengue: A Holistic Review of Virus Classification, Pathophysiology, Diagnosis & Herbal Remedies." International Journal of Pharmaceutical Research and Applications 10, no. 2 (2025): 1829–33. https://doi.org/10.35629/4494-100218291833.

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The virus that causes dengue, known as the dengue virus(DENV),is a member of the Flavivirus genus and is spread by mosquitoes. The mosquitoes Aedesaegypti and Aedesalbopictus are the main vectors of transmission. With an estimated 390 million infections each year worldwide, the disease is common in tropical and subtropical climates. From mild feverish disease (dengue fever) to serious complications like dengue hemorrhagic fever (DHF) and potentially fatal dengue shock syndrome (DSS), dengue can appear with a broad range of clinical symptoms. Skin rashes, retroorbital pain, joint and muscle pai
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Higashida, Randall T., V. Van Halbach, Grant B. Hieshima, and Leslie Cahan. "Cavernous Carotid Artery Aneurysm Associated with Marfan's Syndrome: Treatment by Balloon Embolization Therapy." Neurosurgery 22, no. 2 (1988): 297–300. http://dx.doi.org/10.1227/00006123-198802000-00003.

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Abstract Intracranial aneurysms arising in the region of the cavernous carotid artery are difficult to manage surgically because of the surrounding cavernous sinus. With recent advances in microballoon technology and permanent solidification agents, it is now possible to treat certain intracranial aneurysms by detachable balloons and preserve the parent vessel. A patient with Marfan's syndrome presented with severe retroorbital pain, ophthalmoplegia, and headaches. Cerebral angiography demonstrated a large cavernous carotid artery aneurysm measuring 17 × 9 × 6 mm. This was successfully treated
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Streszczenia konferencji na temat "Retroorbital pain"

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Bernardes, Leonardo de Sousa, Raphael Palomo Barreira, Marina Trombin Marques, Danyelle Sadala Reges, Vivian Dias Baptista Gagliardi, and Rubens José Gagliardi. "Internal Carotid Artery Dissection during Puerperium: A Case Report." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.456.

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Background: Carotid or vertebral artery dissection is a rare puerperium event, occurring in less than 6% of cases. Although physiopathology is not completely understood, it is probably multifactorial involving increased cardiac output, hypervolemia and hormonal changes remodeling endothelium and favoring dissection. Most patients present headache and neck pain, but it is also reported Horner syndrome, tinnitus, retroorbital pain and cranial nerve palsies. Case Report: Female, 39-year-old patient in the 20th day of puerperium presents a sudden headache with transitory left hemiparesis and dysar
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Dück, David Lemke, Marco Antonio Takashi Utiumi, Angelica Beate Winter Boldt, and Elcio Juliato Piovesan. "Clinical features of headaches in an urban Mennonite group in Southern Brazil." In XIV Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2023. http://dx.doi.org/10.5327/1516-3180.141s1.463.

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Introduction: Genetic variants play a pathophysiological role in headaches, especially regarding migraine. The Mennonites are a group that originated during the religious reformation in Europe, during the Sixteenth Century and have been geographically and genetically isolated throughout their history, harboring a distinctive distribution of diseases. Objectives: To determine the clinical features of headaches in a group with direct Mennonite ancestry (MG) contrasting with other urban community members, that share a similar environment (control group, CG). Methods: Subjects with headaches were
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Gaudencio, Julia Loureiro, Hilton Mariano Mariano da Silva Júnior, and Pedro Neves Fortunato. "Ramsay Hunt Syndrome complicated by Cerebral venous thrombosis (case report)." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.222.

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Context: Ramsay Hunt syndrome is a condition caused by the Varicella-Zoster Virus in the geniculate ganglion and leads to peripheral facial nerve palsy and erythematous vesicular rash in the affected area. It is a rare disorder but is the second most common cause of peripheral facial nerve palsy without trauma. Cerebral venous thrombosis is a rare cerebrovascular disease and responsible for only 0.5% of all strokes. Among its causes are oral contraceptives, infection in the central nervous system, systemic inflammations, and thrombophilia. Case report: We report the case of a previously health
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