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Artículos de revistas sobre el tema "Orbital disorders"

Autor: Grafiati
Publicado: 4 de junio de 2021
Última modificación: 28 de julio de 2025

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1

&NA;. "ORBITAL DISORDERS." Ophthalmic Plastic & Reconstructive Surgery 9, Supplement (1993): 31–44. http://dx.doi.org/10.1097/00002341-199301001-00013.

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2

Garner, A. "Orbital lymphoproliferative disorders." British Journal of Ophthalmology 76, no. 1 (1992): 47–48. http://dx.doi.org/10.1136/bjo.76.1.47.

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Shao, Yi, and Xiao-Ming Huang. "Guidelines for standard operation of imaging modalities in orbital diseases (2024)." International Journal of Ophthalmology 18, no. 1 (2025): 51–66. https://doi.org/10.18240/ijo.2025.01.06.

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Orbital disorders include conditions originating from the orbital bones, surrounding tissues, and post-orbital septum. They also include systemic ailments affecting the orbit. Different clinical symptoms make up the complex range of orbital disorders. Because these disorders mostly impact the orbital area instead of the intraocular compartment, there is little diagnostic usefulness for typical ophthalmic visual tests. As such, the vital instruments for diagnosing and evaluating orbital illnesses have become ophthalmic imaging modalities, including ocular ultrasonography (B-scan), computed tomo
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4

Neems, Leslie, Elizabeth L. Echalier, and Prem S. Subramanian. "Orbital Tumors and Inflammatory Disorders." International Ophthalmology Clinics 58, no. 2 (2018): 181–95. http://dx.doi.org/10.1097/iio.0000000000000217.

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5

Valvassori, Galdino E., Sushil S. Sabnis, Rana F. Mafee, Mark S. Brown, and Allen Putterman. "IMAGING OF ORBITAL LYMPHOPROLIFERATIVE DISORDERS." Radiologic Clinics of North America 37, no. 1 (1999): 135–50. http://dx.doi.org/10.1016/s0033-8389(05)70083-x.

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6

Goyal, Pradeep, Steven Lee, Nishant Gupta, et al. "Orbital apex disorders: Imaging findings and management." Neuroradiology Journal 31, no. 2 (2018): 104–25. http://dx.doi.org/10.1177/1971400917740361.

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Orbital apex disorders include orbital apex syndrome, superior orbital fissure syndrome and cavernous sinus syndrome. These disorders result from various etiologies, including trauma, neoplastic, developmental, infectious, inflammatory as well as vascular causes. In the past, these have been described separately based on anatomical locations of disease process; however, these three disorders share similar causes, diagnostic evaluation and management strategies. The etiology is diverse and management is directed to the causative process. This imaging review summarizes the pertinent anatomy of t
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Ali, MohammadJ, and Nandini Bothra. "Orbital involvement in lacrimal drainage disorders." Saudi Journal of Ophthalmology 35, no. 3 (2021): 204. http://dx.doi.org/10.4103/sjopt.sjop_121_21.

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8

McKeown, Craig A. "Ocular Motility Disorders and Orbital Trauma." International Ophthalmology Clinics 32, no. 3 (1992): 123–50. http://dx.doi.org/10.1097/00004397-199203230-00010.

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9

Sevel, David. "Nasolacrimal and orbital disorders in children." Current Opinion in Ophthalmology 3, no. 6 (1992): 759–63. http://dx.doi.org/10.1097/00055735-199212000-00006.

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Bothra, Nandini, and Mohammad J. Ali. "Orbital involvement in lacrimal drainage disorders." Saudi Journal of Ophthalmology 35, no. 3 (2021): 204–8. http://dx.doi.org/10.4103/sjopt.sjopt_121_21.

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Lacrimal sac is situated anterior to the orbital septum, which acts as a barrier, thus limiting the posterior migration of the pathologies affecting the lacrimal drainage system. Certain pathologies can breach this barrier and secondarily involve the orbit causing significant clinical manifestations. This posterior migration of pathology also has a significant influence on the management and outcomes. The present paper will discuss the lacrimal pathologies which secondarily involve the orbit and its influence on the management and outcomes.
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11

Warburton, R. E., C. C. D. Brookes, B. A. Golden, and T. A. Turvey. "Orbital apex disorders: a case series." International Journal of Oral and Maxillofacial Surgery 45, no. 4 (2016): 497–506. http://dx.doi.org/10.1016/j.ijom.2015.10.014.

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12

Ali, Kausar, Kelly Schultz, Douglas Marx, Edward Buchanan, and Larry Hollier. "Secondary Repair of Posttraumatic Enophthalmos and Extraocular Movement Disorders." Facial Plastic Surgery 33, no. 06 (2017): 606–12. http://dx.doi.org/10.1055/s-0037-1608781.

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AbstractEnophthalmos, or recession of the eye posteriorly and inferiorly, is a potential sequela of orbital trauma and a source of significant cosmetic and functional concern. Late enophthalmos occurs when early reconstruction of the bony orbit fails to completely restore normal orbital shape and volume, resulting in aesthetic deformity and persistent diplopia. In this article, we provide a framework for evaluation of posttraumatic enophthalmos and outline the surgical principles of secondary repair necessary to optimize globe position. With implementation of proper craniofacial exposure, oste
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13

Nezu, Naoya, Yoshihiko Usui, Masaki Asakage, et al. "Distinctive Tissue and Serum MicroRNA Profile of IgG4-Related Ophthalmic Disease and MALT Lymphoma." Journal of Clinical Medicine 9, no. 8 (2020): 2530. http://dx.doi.org/10.3390/jcm9082530.

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The molecular pathogenesis of orbital lymphoproliferative disorders, such as immunoglobulin G4-related ophthalmic disease (IgG4-ROD) and orbital mucosa-associated lymphoid tissue (MALT) lymphoma, remains essentially unknown. Differentiation between the two disorders, which is important since the work-up and treatment can vary greatly, is often challenging due to the lack of specific biomarkers. Although miRNAs play an important role in the regulation of carcinogenesis and inflammation, the relationship between miRNA and orbital lymphoproliferative diseases remains unknown. We performed a compr
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14

Kahana, Alon. "Orbital inflammatory disorders: new knowledge, future challenges." Current Opinion in Ophthalmology 32, no. 3 (2021): 255–61. http://dx.doi.org/10.1097/icu.0000000000000743.

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15

Dutta, Paromita, Prateek Kumar, Vaibhav Nagpal, Kamlesh Anand, Avani Hariani, and Ashish Krishnan. "Pseudo orbital apex disorders: Two case reports." Indian Journal of Ophthalmology - Case Reports 1, no. 2 (2021): 379. http://dx.doi.org/10.4103/ijo.ijo_2353_20.

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16

Maurya, Rajendra Prakash. "Radiation therapy for benign oculo-orbital disorders." IP International Journal of Ocular Oncology and Oculoplasty 7, no. 3 (2021): 229–30. http://dx.doi.org/10.18231/j.ijooo.2021.047.

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17

Gorospe, Luis, Ar�nzazu Royo, Teresa Berrocal, Pilar Garc�a-Raya, Pilar Moreno, and Jos� Abelairas. "Imaging of orbital disorders in pediatric patients." European Radiology 13, no. 8 (2003): 2012–26. http://dx.doi.org/10.1007/s00330-002-1738-y.

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18

Lebădă, Ioana-Codruţa, and Mihaela Stanciu. "The Efficiency of Pulse Therapy with Glucocorticoids in Inflammatory Orbital Disorders: Case Report." Acta Medica Transilvanica 25, no. 4 (2020): 22–24. http://dx.doi.org/10.2478/amtsb-2020-0063.

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Abstract Orbital pseudotumor represents a benign inflammatory disorder of the orbit, with unspecified etiology, whose clinical presentation can mimic the ocular pathology of Basedow disease, namely Graves’ ophthalmopathy, the two of them representing two of the most common orbital conditions. Imagistic methods and laboratory analyses can establish the diagnosis through orbital MRI images specific for the orbital pseudotumor, especially by dosage of the TSH receptor antibodies (TRAb) which will have increased values in Basedow disease with ocular damage. In both situations, the treatment is rep
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19

Brar, Gagandeep K., Jigu S. Krishn, NR Gupta, Archana Prabha, Parvi Phutela, and Charu Chadha. "Non specific orbital inflammatory disease – A review article." IP International Journal of Ocular Oncology and Oculoplasty 8, no. 2 (2022): 115–19. http://dx.doi.org/10.18231/j.ijooo.2022.024.

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Non Specific Orbital Inflammatory Disease (NSOID) is a benign, noninfective inflammatory condition of the orbit which does not have any identifiable local or systemic causes. Orbital pseudotumor was first described in 1903 by Gleason. The clinical diagnosis is one of exclusion with evaluation directed to exclude neoplasms, infections and systemic disorders. IOI is diagnosed by clinical history and evaluation to rule out other causes of orbital disease. Orbital pseudotumor is the third most common orbital disease following Graves ophthalmopathy and lymphoproliferative disease.
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20

Ali, Hussein Abbas, Ali Moheiseen Al-Taee Rajaa, J.I. Al-Shammari Mohammed, and A. Al-fahham Ali. "Epidemiology and Classification of Cystic Benign Orbital Tumors: A Review Article." INTERNATIONAL JOURNAL OF HEALTH & MEDICAL RESEARCH 03, no. 08 (2024): 573–77. https://doi.org/10.5281/zenodo.13283243.

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Benign orbital tumor is known to be with a broad variation in the clinical features and findings. Tumors in this small cavity could quickly result in crucial symptoms in vision, even though complete loss of vision. These tumors may be infectious, inflammatory or neoplastic. Management and follow up may differ based on the tumor type, site, and spread into other systems. Because of what is known that the orbital cavity constitutes a small space, so that tiny projections like that observed with tumors and infection could result in huge physiologic disorders in near structures leading to anatomic
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21

Rashid, Riffat, Sadia Sultana, Farzana Afzal, and Syeed Mehbub Ul Kadir. "Diagnostic and Therapeutic Approaches of Orbital Inflammatory Disease: A Systematic Review." Journal of National Institute of Ophthalmology 6, no. 2 (2025): 73–82. https://doi.org/10.3329/jnio.v6i2.80324.

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Background: Orbital inflammatory disease (OID) is a group of disorders characterized by in-flammation in the orbit, which can affect various orbital structures, including the extraocular muscles, lacrimal glands, and orbital fat. One specific subset, pure orbital inflammation, is char-acterized by isolated inflammatory processes within the orbital tissues without the involvement of other systemic or regional disorders. The condition typically presents with symptoms such as pain, proptosis, and diplopia. Early diagnosis and appropriate management are crucial to pre-venting permanent damage to t
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22

Takahira, Masayuki, Yoshiaki Ozawa, Mitsuhiro Kawano, et al. "Clinical Aspects of IgG4-Related Orbital Inflammation in a Case Series of Ocular Adnexal Lymphoproliferative Disorders." International Journal of Rheumatology 2012 (2012): 1–5. http://dx.doi.org/10.1155/2012/635473.

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The most frequent ocular adnexal tumors and simulating lesions are lymphoproliferative disorders (LPDs), including malignant lymphomas and orbital inflammation with lymphoid hyperplasia or infiltration. IgG4-related orbital inflammation (IgG4-ROI) often involves lacrimal glands and other orbital tissues and is an important differential diagnosis. The present study evaluated clinical aspects of IgG4-ROI in a case series of orbital LPD. Sixty-two consecutive cases of orbital LPD, pathologically diagnosed from November, 2004, through March, 2011, were investigated. Histological types were 22 case
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23

Gausas, Roberta. "DIAGNOSIS AND MANAGEMENT OF OCULOPLASTIC AND ORBITAL DISORDERS." Ophthalmic Surgery, Lasers and Imaging Retina 29, no. 11 (1998): 951. http://dx.doi.org/10.3928/1542-8877-19981101-15.

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24

Guerra, Roberto. "Orbital and nasolacrimal disorders and retinoblastoma in children." Current Opinion in Ophthalmology 2, no. 6 (1991): 663–71. http://dx.doi.org/10.1097/00055735-199112000-00002.

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25

Sires, Bryan S. "Diagnosis and Management of Oculoplastic and Orbital Disorders." Archives of Ophthalmology 115, no. 7 (1997): 948. http://dx.doi.org/10.1001/archopht.1997.01100160118036.

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26

Dallalzadeh, Liane O., Emily G. Robillard, Kendall Goodyear, and Monica R. Khitri. "Eyelid, Orbital, and Lacrimal Disorders in the Neonate." NeoReviews 24, no. 10 (2023): e616-e625. http://dx.doi.org/10.1542/neo.24-10-e616.

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27

Maurya, Rajendra P., Kajal Pal, Syeed Mehbub Ul Kadir, et al. "Orbital apex syndrome: A review." IP International Journal of Ocular Oncology and Oculoplasty 8, no. 4 (2023): 229–36. http://dx.doi.org/10.18231/j.ijooo.2022.051.

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An orbital apex syndrome (OAS) has been described previously as a syndrome involving damage to the ocular motor and sensory nerves in association with optic nerve dysfunction. Patients usually present with signs and symptoms derived from the involvement of structures within the orbital apex, the superior orbital fissure, and the cavernous sinus. Visual loss from optic neuropathy and ophthalmoplegia involving multiple cranial nerves are the hallmarks of orbital apex syndrome. Historically, superior orbital fissure, orbital apex, and cavernous sinus are being used to define the anatomical locati
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28

Hsu, Jennifer, and Brian G. Mohney. "Infantile Hemangiomas Masquerading as Other Periocular Disorders." Case Reports in Pediatrics 2012 (2012): 1–3. http://dx.doi.org/10.1155/2012/290645.

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Periocular tumors are common in infancy. The most common periocular tumors are capillary hemangiomas, which are present in 1-2% of newborns and develop in 10%–12% of children by the age of 1 year old. Deep capillary hemangiomas may be more challenging to diagnose than superficial capillary hemangiomas and can be confused with other orbital lesions. Deep orbital hemangiomas can mimic teratoma, lymphangioma, rhabdomyosarcoma, metastatic neuroblastoma, and granulocytic sarcoma. In this paper, we describe 2 pediatric cases where previously diagnosed dermoid cyst and dacrocystocele were found to be
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29

Shi, Caiping, Jia Feng, Sujuan Zhao, et al. "Orbital Lymphoproliferative Disorders (OLPDs) in a 3-year-old Child: Case Report and Review of Literature." Archives of Clinical Ophthalmology 3, no. 1 (2023): 13–19. http://dx.doi.org/10.33696/ophthalmology.3.011.

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Background: Orbital lymphoproliferative disorders (OLPDs) consist of a spectrum of diseases ranging from benign to malignant lesions including reactive lymphoid hyperplasia, atypical lymphoid hyperplasia, and lymphoma. OLPDs rarely present as an orbital mass lesion in children. Accurate discrimination of OLPDs is crucial for treatment planning. We report a case to investigate the clinical and pathological features of OLPDs in children. Case presentation: A 3-year-old female with orbital mass was admitted to the hospital and proceeded to have a CT orbit which showed an orbital mass. The orbital
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30

Mehlan, Juliane, and Frank Schüttauf. "Infranuclear Eye Movement Disorders." Klinische Monatsblätter für Augenheilkunde 238, no. 11 (2021): 1178–85. http://dx.doi.org/10.1055/a-1615-2267.

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AbstractInfranuclear motility disorders are such of the cranial nerves, the extraocular muscles or changes in the orbit but definitely peripheral to the nuclei of the cranial nerves. Characteristic are movement deficits, a compensatory head posture and the pattern of incomitancy. The secondary angle of deviation is usually larger than the primary. Combined pareses suggest a lesion in the cavernous sinus, orbital apex or a multilocular event. It is essential to rule out supranuclear disorders, especially if the motility deficit is atypical. For clarification, an individual risk assessment is re
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31

Sathyalakshmi M H and Girish F Hongal. "ENT Disorders Presenting with Ophthalmological Manifestations:An Overview." Asian Journal of Medical Research 9, no. 1 (2020): OT12—OT16. http://dx.doi.org/10.47009/ajmr.2020.9.1.ot4.

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Background: It is important to diagnose the condition early and manage aggressively. It is often difficult to cure orbital cellulitis due to late treatment and may cause blindness if left untreated because of optic nerve compression. Both orbital abscess and cavernous sinus thrombosis may lead to intracranial spread of infection, such as meningitis or cerebral abscess with high morbidity and possible mortality.Subjects and Methods:A total number of 124 cases of ophthalmological manifestation caused by various ENT diseases, mostly paranasaltumourextensions; nasopharyngeal tumour and furunculosi
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Rodrigues, Thiago Pereira, Mariana Athaniel Silva Rodrigues, Daniel de Araújo Paz, et al. "Orbitofrontal sulcal and gyrus pattern in human: an anatomical study." Arquivos de Neuro-Psiquiatria 73, no. 5 (2015): 431–44. http://dx.doi.org/10.1590/0004-282x20150048.

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The anatomical characterization of the orbitofrontal cortex in human is limited in literature instead of many functional and clinical studies involving it. Objective Anatomically define the orbitofrontal region aiming to possible neurosurgical treatments and unify the scientific nomenclature as well. Method We analyze eighty four human hemispheres using a surgical microscope. Then we chose four hemispheres and dissect them according to Klinger’ technique. Results We found five main sulcus: olfatory sulcus, orbital medial sulcus, orbital lateral sulcus, orbital transverse sulcus and orbital int
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33

Haradome, K., H. Haradome, Y. Usui, et al. "Orbital Lymphoproliferative Disorders (OLPDs): Value of MR Imaging for Differentiating Orbital Lymphoma from Benign OPLDs." American Journal of Neuroradiology 35, no. 10 (2014): 1976–82. http://dx.doi.org/10.3174/ajnr.a3986.

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34

Jayamurthy, Pavithra, Renuga Devi, P. Nallamuthu, and Vinitha Angalan. "Secondaries from retromolar trigone carcinoma leading to orbital apex disorders." Global Journal of Health Sciences and Research 1 (February 20, 2023): 48–50. http://dx.doi.org/10.25259/gjhsr_11_2022.

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Orbital apex disorders (OADs) are uncommon and they include – orbital apex syndrome (OAS), superior orbital fissure syndrome (SOFS), and cavernous sinus syndrome (CSS). They all share similar etiologies, diagnostic evaluation, and management strategies. These syndromes can occur isolated or combined – where SOFS progresses and develops into OAS or CSS. Combined presentation has been reported with infective etiologies, but no literature is available for neoplasms. OAD secondary to head and neck cancer is exceptionally rare. A 44-year-old male post left hemi-mandibulectomy with modified neck dis
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35

Takahashi, Tsutomu, Mihoko Nakamura, Yumiko Nishikawa, et al. "Decreased number of orbital sulci in schizophrenia spectrum disorders." Psychiatry Research: Neuroimaging 250 (April 2016): 29–32. http://dx.doi.org/10.1016/j.pscychresns.2016.03.005.

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36

Krauss, Howard R. "Orbital Surgical Guidelines—Clinical Evaluation." Journal of Neurological Surgery Part B: Skull Base 82, no. 01 (2021): 129–41. http://dx.doi.org/10.1055/s-0040-1722699.

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AbstractOrbital disorders may present with change in form or function or may be discovered incidentally during clinical or imaging evaluations. A standardized orbital clinical examination, with appropriate ancillary tests, is helpful in narrowing the differential diagnosis and in the development of plans for management, with an eye toward minimizing the morbidity of the disease or its treatment. Evaluation and management may best be performed with a multidisciplinary team, which has become more common in skull base surgery.
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Carmody, R. F., R. Khan, R. K. Shastri, B. A. Winegar, and M. F. Mafee. "Lymphoproliferative Disorders of the Orbit and Ocular Adnexa." Neurographics 10, no. 5 (2020): 329–42. http://dx.doi.org/10.3174/ng.2000022.

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Lymphoma is the most common malignancy to affect the orbit and is frequently a diagnostic challenge for the radiologist. Any orbital and/or ocular adnexal structure may be involved with lymphoproliferative disease, and many conditions, such as idiopathic orbital inflammation and metastatic disease, may have a similar appearance on CT or MR imaging. Almost all ocular adnexal lymphomas are of the non-Hodgkin B-cell type. These vary in aggressiveness from the low-grade mucosa-associated lymphoid tissue type lymphoma to the highly malignant mantle-cell lymphoma, which is a disseminated disease wit
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Al-Ghazzawi, Karim, Sven Holger Baum, Roman Pförtner, et al. "Evaluation of Orbital Lymphoproliferative and Inflammatory Disorders by Gene Expression Analysis." International Journal of Molecular Sciences 23, no. 15 (2022): 8609. http://dx.doi.org/10.3390/ijms23158609.

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Non-specific orbital inflammation (NSOI) and IgG4-related orbital disease (IgG4-ROD) are often challenging to differentiate. Furthermore, it is still uncertain how chronic inflammation, such as IgG4-ROD, can lead to mucosa-associated lymphoid tissue (MALT) lymphoma. Therefore, we aimed to evaluate the diagnostic value of gene expression analysis to differentiate orbital autoimmune diseases and elucidate genetic overlaps. First, we established a database of NSOI, relapsing NSOI, IgG4-ROD and MALT lymphoma patients of our orbital center (2000–2019). In a consensus process, three typical patients
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Zagórski, Karol, Nina Skalska-Dziobek, Przemysław Cetnarowski, et al. "Eye Symptoms in Parathyroid Disorders: Clinical Presentation and Research Perspectives." Quality in Sport 39 (March 8, 2025): 58991. https://doi.org/10.12775/qs.2025.39.58991.

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Introduction and purpose: Endocrine disorders often affect multiple organs, frequently presenting with characteristic ophthalmic symptoms. Ocular abnormalities occur in both hyperparathyroidism and hypoparathyroidism, potentially affecting nearly all parts of the eyeball and orbital structures. This study aims to summarize available literature and recent findings on ophthalmic manifestations linked to parathyroid disorders. Material and methods: A comprehensive literature review was conducted using keywords in the PubMed database, the Via Medica journal database, the Polish Society of Endocrin
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40

Maurya, Rajendra Prakash, Ajay Kumar Yadav, Shivam Tiwari, et al. "Effects of SARS-Cov-2 infection and rhino-orbital mucormycosis on concentrations of inflammatory biomarkers in Indian populations." Indian Journal of Clinical and Experimental Ophthalmology 8, no. 4 (2022): 450–57. http://dx.doi.org/10.18231/j.ijceo.2022.093.

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Rhino-orbital mucormycosis is a rare life threatening invasive fungal infection that has recently shown a very high mortality rate in India during COVID-19 pandemic. We have designed the present study to find out associations between COVID-19 induced rhino-orbital mucormycosis and concentrations of inflammatory markers, i.e. D-dimer, Ferritin, IL-6, CRP and PCT, in blood serum of Indian population.There were four groups in the study, viz. control group with healthy subjects, treatment group-1 with patients suffering from SARS-COV-2 infection, treatment group-2 with patients suffering from both
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41

Ma, Jingying, Zhenxiao Huang, and Bing Zhou. "Transnasal Endoscopic Resection of Pediatric Orbital Cyst: “How I do it”." American Journal of Rhinology & Allergy 32, no. 1 (2018): 71–73. http://dx.doi.org/10.2500/ajra.2018.32.4491.

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Background An orbital cystic lesion is a common orbital disease and has classically been approached via external incision. The introduction of endoscopic surgery has revolutionized the management of sinus and skull base disorders. Similarly, endoscopic techniques have been increasingly used to access intraorbital lesions with excellent outcomes, especially in pediatric patients. Objective We described, in detail, the surgical technique of the endoscopic approach to treat a pediatric orbital cyst. Results The cyst was completely resected, and the patient quickly recovered without any complicati
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Asghar, Adnan, and Muhammad Awais. "ENDOSCOPIC SINUS SURGERY;." Professional Medical Journal 24, no. 08 (2017): 1248–52. http://dx.doi.org/10.29309/tpmj/2017.24.08.1002.

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Background: Endoscopic sinus surgery has become a preferred modalityfor management of various nasal and sinus disorders. Orbital complications, though rare,are reported amongst patients undergoing ESS. Study Design: Case series. Methods: Aretrospective review was undertaken of four cases of orbital complications during endoscopicsinus surgery. Results: Two patients suffered from periorbital haematoma and subconjunctivalhaemorrhage. One patient developed subcutaneous emphysema and numbness of lower eyelidand cheek. One patient got oedema of lower eyelid. Conclusion: Ophthalmic complicationsoccu
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43

Sudrajat, Nandang, and Delfitri Lutfi. "Difficulty in Management of Advanced Pediatric Orbital Tumor." Vision Science and Eye Health Journal 1, no. 1 (2021): 6–9. http://dx.doi.org/10.20473/vsehj.v1i1.2021.6-9.

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Introduction: Tertiary care centers often manage pediatric orbital tumors, especially in advanced lesions and complex management. We report a case of a young boy with a malignant orbital tumor involving intracranial infiltration. Case presentation: A four-year-old boy had proptosis on the left eye for two months accompanied with blurred vision, pain, and oftenly bleeds with ipsilateral nasal congestion. There was no history of trauma, eye disorders, systemic diseases, or growth disorders. The physical examination showed stable vital signs, however a weak general condition and no enlarged regio
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44

Pavani, Adi S. S., Sileveru C. Mouli, Varanasi Swetha, and Karishma. "Orbital apex syndrome secondary to sinusitis." International Journal of Otorhinolaryngology and Head and Neck Surgery 10, no. 6 (2024): 770–72. http://dx.doi.org/10.18203/issn.2454-5929.ijohns20243526.

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The orbital apex disorders include superior orbital fissure syndrome, cavernous sinus syndrome, and orbital apex syndrome. A 50-year female patient presented to hospital with complaints of right eye heaviness since 3 days, decrease vision since 5 days. Right sided headache, right eye blurred vision, ptosis of right eye lid for 1 week. On ophthalmologic examination ptosis and blurred vision in right eye seen. Visual acuity in right eye shows counting fingers close to fingers (CFCF), exotropia, extraocular movements reduced. Computed tomography paranasal sinus (CT PNS) plain and contract showed
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Presutti, Livio, Daniela Lucidi, Federico Spagnolo, Giulia Molinari, Silvia Piccinini, and Matteo Alicandri-Ciufelli. "Surgical multidisciplinary approach of orbital complications of sinonasal inflammatory disorders." Acta Otorhinolaryngologica Italica 41, Suppl. 1 (2021): S108—S115. http://dx.doi.org/10.14639/0392-100x-suppl.1-41-2021-11.

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Ruiters, Sébastien, and Ilse Mombaerts. "Applications of three-dimensional printing in orbital diseases and disorders." Current Opinion in Ophthalmology 30, no. 5 (2019): 372–79. http://dx.doi.org/10.1097/icu.0000000000000586.

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RANIA A. ABDEL SALAM, M.D., MAY I. EL-RASHEDY, M. Sc, and IHAB S. OTHMAN, M.D. "Evaluation of Surgical-Navigation System in Management of Orbital Disorders." Medical Journal of Cairo University 87, June (2019): 1349–55. http://dx.doi.org/10.21608/mjcu.2019.53425.

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Guyennet, Eloïse, Jean-Laurent Guyomard, Emilie Barnay, Franck Jegoux, and Jean-François Charlin. "Cephalic Tetanus from Penetrating Orbital Wound." Case Reports in Medicine 2009 (2009): 1–3. http://dx.doi.org/10.1155/2009/548343.

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Tetanus is a neurologic disorder caused by tetanospasmin, a protein toxin elaborated by Clostridium tetani. Cephalic tetanus is a localized form of the disease causing trismus and dysfunction of cranial nerves. We report the case of a man who presented with facial trauma, complete ophthalmoplegia, exophthalmos, areactive mydriasis, and periorbital hematoma. An orbital CT revealed air bubbles in the right orbital apex. The patient was given a tetanus toxoid booster and antibiotherapy. After extraction of a wooden foreign body, the patient developed right facial nerve palsy, disorders of swallow
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Bhattacharjee, Bappaditya, Roopal Srivastava, Rajesh Bansal, and Naresh K. Sharma. "Fabrication of orbital prosthesis by two different methods in patients with post-COVID-19 rhino-orbital maxillary mucormycosis: A case series." National Journal of Maxillofacial Surgery 15, no. 1 (2024): 164–67. http://dx.doi.org/10.4103/njms.njms_183_22.

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ABSTRACT Neoplasms, congenital disorders, fungal infections, and traumatic injuries are the predominant causes of orbital defects. Various retentive mechanisms such as application of adhesive, utilization of mechanical undercuts, and implant-supported attachments are generally used in the maxillofacial prosthesis. In the orbital region, the result of magnet-retained attachments is favorable compared with other mechanisms. Different advantages of the magnet-retained prosthesis are less manual dexterity needed during insertion or removal and better maintenance of hygiene. The skin–implant interf
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Lystratenko, O. I., A. M. Kardash, D. O. Lystratenko, A. V. Vashchenko, and O. F. Smyrnova. "Diagnosis and Surgical Treatment of Orbital Tumors of Various Localizations and Histostructures." Neuroscience and Neurological Surgery 6, no. 1 (2020): 01–11. http://dx.doi.org/10.31579/2578-8868/111.

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The article reviews and analyzes the results of treatment of 32 patients with orbital tumors operated in the clinic, neurosurgery until the period from 2015 till September 2019. Goals and objectives: coverage of clinical signs and symptoms, histology, diagnostic methods and treatment of patients operated on with orbital tumors during the period 2015-2019. Determination of optimal surgical approach to the tumors with different localization for performing the radical organ-preserving surgery, with maximal saving of visual functions, minimization of oculomotor disorders, patient disability. Mater
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