Gotowe bibliografie tematyczne / Ocular oncology and case report

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Gotowa bibliografia na temat „Ocular oncology and case report”

Autor: Grafiati

Data publikacji: 2 czerwca 2025

Data aktualizacji: 19 lipca 2025

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Artykuły w czasopismach na temat "Ocular oncology and case report"

Nixon, Nisha, Vaidehi Konteti, Karan Gupta, Anna Thompson, Erika Damato, and Madhavan Rajan. "Severe Ocular Adverse Reaction Following Single Pembrolizumab Infusion: A Case Report." Clinics of oncology 07, no. 12 (2024): 01–04. http://dx.doi.org/10.47829/coo.2024.71201.

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1.1. Purpose: To report a case of severe sight loss following single infusion of pembrolzumab 1.2. Methods: Retrospective case report 1.3. Results: Ocular adverse events associated with immune checkpoint inhibitors, due to their rarity, remain poorly characterised. Pembrolizumab targets the programmed cell death (PD-1) protein on T cells, circumventing the mechanisms by which cancer cells evade the body’s adaptive immune response. To date, reports of ocular surface disease, neuro-ophthalmic complications, orbitopathy, retinal dysfunction and uveitis have been reported following pembrolizumab infusion. We report the first case of severe panuveitis resulting in loss of vision, following a single initial infusion of pembrolizumab. 1.4. Conclusion: The case serves as a heartening reminder of the need for prompt reporting of visual symptoms, recognition of ocular immune-related adverse events and a multi-disciplinary approach between oncology and ophthalmology in patients receiving immunotherapy for cancer treatment.

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F, Guido. "Bilateral Sclerochoroidal Calcifications: A Case Report." Open Access Journal of Ophthalmology 8, no. 1 (2023): 1–5. http://dx.doi.org/10.23880/oajo-16000278.

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Purpose: The aim of this case report is to describe a rare condition of bilateral sclerochoroidal calcification Case Report: A 79 years old asymptomatic Caucasian female was referred to our Ocular Oncology Center of the Ophthalmic Surgery Department of Pisa on November 2021. She was in apparent good health. Funduscopic examination revealed yellowwhite irregular lesions in the supero-temporal quadrant of both eyes. Best-corrected visual acuity was 20/20. B-scan and A-scan ultrasound revealed hyper-echoic solid lesions with acoustic orbital shadowing measuring 1.5 mm in thickness and 4.6 mm in diameter, on average. Enhanced Deep Imaging Optical Coherence Tomography showed a scleral lesion compatible with the presence of deposition of calcium with Table Mountain and rolling pattern. Fluorescein angiography revealed hypofluorescence in the arterial phase and a mild hyper-fluorescence in the venous phase with persistent late staining. Indocyanine green angiography showed hypo-fluorescence at the early, middle, and late phases. Systemic investigation of calcium and phosphate metabolism was performed and the patient didn’t display any underlying systemic disorder. Conclusion: It is important to know and recognize this condition. Although most cases of sclerochoroidal calcifications may be idiopathic, systemic laboratory workup must be performed to exclude calcium-phosphate metabolic disorder that can be associated to these ocular signs. Given the rare possible development of choroidal neovascularization, regular imaging checkup is recommended.

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Blanchard, Sierra, Suzzane Li, and Danielle Weiler. "Erdafitinib-associated Central Serous Chorioretinopathy: A Case Report." Canadian Journal of Optometry 84, no. 4 (2022): 35–40. http://dx.doi.org/10.15353/cjo.v84i4.4349.

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Erdafitinib is a pan-fibroblast growth factor receptor (FGFR) kinase inhibitor approved to treat patients with metastatic or advanced urothelial carcinoma and is being developed for the treatment of other cancer types. This oral chemotherapeutic agent carries a warning for potential ocular adverse reactions including central serous chorioretinopathy and dry eyes. This case report describes an 88-year-old Caucasian male co-managed in the eye clinic over the course of treatment with erdafitinib for metastatic urothelial carcinoma. The patient developed asymptomatic episodes of recurring and remitting bilateral central serous chorioretinopathy correlating to erdafitinib dose modifications and interruptions. It is crucial for eye care providers to recognize the potential ocular adverse events related to erdafitinib, its drug class, and medications which target similar pathways. Effective communication and careful co-management with oncology is essential in providing quality care to this subset of patients. With the care coordination, an effective yet tolerable dosing may provide the patient with increased survival rate and improved quality of life.

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Czyz, Craig, Kyle Blair, and Reece Bergstrom. "Leptomeningeal Carcinomatosis with Delayed Ocular Manifestations." Case Reports in Oncology 14, no. 1 (2021): 98–100. http://dx.doi.org/10.1159/000510808.

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The most common presenting symptoms of leptomeningeal carcinomatosis (LC) are ocular manifestations with vision loss. There are multiple reports of undiagnosed LC causing sudden, complete, monocular vision loss as the presenting symptom; however, sudden bilateral vision loss 6 months following diagnosis has not been described. Any new ocular involvement or worsening of previous ocular symptoms warrants reimaging and prompt ophthalmology consultation, as this likely indicates disease progression. This report details a unique case of LC where a previously diagnosed patient developed sudden, complete, bilateral vision loss and multiple cranial nerve palsies with progression of LC on imaging.

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Patidar, Yaman, Smitha C. Saldhana, M. C. Suresh Babu, et al. "Symptomatic orbital metastasis as an initial presentation of adenocarcinoma lung: A case report and review of literature." Lung India 41, no. 5 (2024): 375–78. http://dx.doi.org/10.4103/lungindia.lungindia_60_24.

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ABSTRACT Orbital metastasis is a rare entity in oncology. With increasing awareness and advancement, patients with initial ocular presentation can be diagnosed and treated. Ocular metastasis is more common in breast cancer followed by lung cancer. Lung cancer with ocular presentation generally have poor prognosis because of difficult diagnosis, Vision impairment and delayed management. Here, we report one such case of 59 year old female presented with painful periorbital swelling in left eye for 3 months with no pulmonary symptoms. On evaluation, she was diagnosed as ocular metastasis with primary being lung adenocarcinoma. Through this case, we enlighten the epidemiology, presentation, clinical features and evaluation of such patients which might help clinicians in further management.

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Bhattarai, Sarita, Susmina Maharjan, Reeya Shah, and Anju Shrestha. "A Case of Leukemic Retinopathy." International Journal of Silkroad Institute of Research and Training 2, no. 2 (2024): 115–17. https://doi.org/10.3126/ijsirt.v2i2.74374.

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This case report describes a 4-year-old male with a known history of acute leukemia, presenting with blurred vision in both eyes following chemotherapy. On examination, the child exhibited central, steady, and maintained vision, with findings suggestive of leukemic retinopathy, including scattered retinal infiltration, vitreous cells, and exudative retinal detachment in both eyes. Leukemic retinopathy, a rare ocular manifestation of leukemia, often arises from the direct infiltration of leukemic cells and is more commonly seen in acute leukemia. Ocular involvement, which may include retinal hemorrhages, cotton wool spots, and tortuous veins, can serve as an indicator of disease progression and affect prognosis. The patient was managed with topical steroids for vitritis and referred to oncology for systemic reassessment. This case highlights the importance of recognizing ocular involvement in leukemia, as the eye can reveal direct signs of leukemic infiltration and aid in early diagnosis or monitoring of relapse. Close collaboration between ophthalmologists and hematologists is crucial for optimizing patient care and improving both visual and overall outcomes.

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Colaço, Raul, Mariana Portela, Ilda Costa, Marta Guedes, and António Mota. "Radiotherapy as Salvage Treatment in Intraocular Lymphoma: A Case Report." Case Reports in Oncology 14, no. 1 (2021): 184–89. http://dx.doi.org/10.1159/000512216.

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A 67-year-old previously healthy woman presented with progressive visual impairment including bitemporal hemianopsia. A brain magnetic resonance imaging revealed a contrast-enhancing mass in the optic chiasm, spreading along the left optic tract. The patient underwent a transcranial biopsy of the left optical tract that yielded a diagnosis of diffuse large B-cell lymphoma. CT scans of the chest, abdomen, and pelvis, PET-CT, and bone marrow biopsy revealed no evidence of systemic lymphoma. Thus, the final diagnosis was of primary central nervous system lymphoma of the optic chiasm. Systemic treatment was initiated with full response. Six months after the end of the treatment, recurrence at cerebellum parenchyma and left tentorium was recorded. A new systemic treatment achieved full response. A second recurrence was noted in an optical coherence tomography of the right eye, 2 years after the initial diagnosis. The patient was treated with intravitreal methotrexate with initial success, but eventual failure after 10 months. Intravitreal rituximab was used with no effect. The patient was then referred to radiotherapy and underwent external beam radiotherapy with VMAT. There were no acute toxicities to report. After the radiotherapy treatment, at 1-year follow-up, the patient has no evidence of disease. Long-term toxicities were recorded and are considered manageable. The present case emphasizes the role of ocular irradiation as an option in the management of intraocular lymphoma patients, including in the salvage setting, with an acceptable ocular toxicity profile.

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Acuña, María del Valle, Mariela Ogusuku, and Walter Briggiler. "Síndrome de Gorlin y afectación ocular." Oftalmología Clínica y Experimental 18, no. 2 (2025): e236-e242. https://doi.org/10.70313/2718.7446.v18.n2.424.

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Objectives: To describe the clinical and ophthalmologic features of Gorlin's syndrome, based on a case report. Case report: A 58-year-old male patient with a history of facial melanoma, who had left frontotemporal myiasis on hyperpigmented lesion and palpebral involvement, in addition to malformation of teeth and multiple facial nodular hyperpigmented lesions was consulted. Vision was severely compromised. After consultation with the head and neck surgery, oncology and dentistry services, a presumptive diagnosis of Gorlin's syndrome was made, based on the multisystemic signs observed. The patient left the clinic and returned three months later with worsening of the fourth episode. A CT scan showed a mass occupying the vertex of the left orbit. It was decided to hospitalize him, due to the clinical and social context of the patient. Surgical toilette was performed, biopsies were taken and future therapeutic guidelines were evaluated, including the use of Vismodegib as an option, but they could not be performed since the patient signed his voluntary discharge and has not returned to the institution. Conclusion. In the case presented, the main characteristics of Gorlin syndrome were identified by means of interconsultations between different specialties: basal cell carcinomas in different regions, mandibular keratocystic tumors and skeletal anomalies, together with ophthalmologic manifestations. Unfortunately, due to social conditions it was not possible to follow up the case.

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Davila, Jose R., and Prithvi Mruthyunjaya. "Updates in imaging in ocular oncology." F1000Research 8 (October 1, 2019): 1706. http://dx.doi.org/10.12688/f1000research.19979.1.

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Innovations in ophthalmic imaging have made a profound impact on the diagnosis and treatment of ophthalmic disease. In ocular oncology, the development of optical coherence tomography with enhanced depth imaging and swept source technologies has made it possible to visualize the anatomical characteristics of retinoblastoma and uveal melanoma with a level of detail previously unobtainable on clinical exam alone. As a result, our understanding of the pathophysiology of vision loss in choroidal melanoma in particular has improved. These modalities have also helped identify fundoscopically “invisible” tumors and risk stratify pre-malignant choroidal lesions, making a strong case for their inclusion in all screening evaluations. Optical coherence tomography angiography, on the other hand, has allowed non-invasive imaging of the retinal and uveal vasculatures, providing insight into vascular changes associated with malignant transformation and vision loss following exposure to radiation. While the impact of new imaging technologies on clinical outcomes and overall survival in ocular oncology has yet to be determined, several reports cited herein offer promising results.

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Batis, Vasilios, James Shuttleworth, Garry Shuttleworth, and Gwyn Samuel Williams. "Diagnostic dilemma of ocular lymphoma." BMJ Case Reports 12, no. 6 (2019): e229513. http://dx.doi.org/10.1136/bcr-2019-229513.

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We report a very unusual presentation of primary intraocular lymphoma masquerading as anterior uveitis with atypical symptoms. A 68-year-old man, initially presented with a 4-day history of painless, left blurred vision. Examination revealed 2 or more anterior chamber cells, mutton-fat keratic precipitates and posterior synechiae. Treatment was initiated, the eye settled, and the patient was discharged. He re-presented 7 months later with hypopyon, a hazy cornea, fibrin deposits and a narrowed anterior chamber angle. Over the coming weeks, it became apparent that the temporal iris was thickened, involving the angle, and his intraocular pressure increased despite topical dorzolamide. Following advice from a tertiary centre and referral to a regional ocular oncology centre, a transscleral biopsy was performed and suggested a ciliary body melanoma. Enucleation was advised and performed, with histological examination revealing features consistent with an ocular diffuse large B-cell lymphoma not involving the optic nerve, sclera or cornea. This is the first ever published report of a case of ocular lymphoma masquerading in this way.

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Rozprawy doktorskie na temat "Ocular oncology and case report"

Ververis, Megan, Ahmed Minhas, Elnora MD Spradling, and Laura MD Stewart. "A Case Report of Krukenberg Tumor Arising From Small Bowel Adenocarcinoma." Digital Commons @ East Tennessee State University, 2018. https://dc.etsu.edu/asrf/2018/schedule/67.

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Case Report: Krukenberg tumor is a metastatic adenocarcinoma of the ovary that classically arises from the gastrointestinal tract, most often as a metastasis from the stomach as the primary origin, followed by colon. Krukenberg tumors are very rare malignant tumors of the ovary, only accounting for 1-2% of all ovarian malignancies. They tend to present with bilateral involvement. The most common presenting symptoms are abdominal pain, distention, and ascites, secondary to the large ovarian masses. Postmenopausal vaginal bleeding is a rare presenting symptom of a Krukenberg tumor. The diagnosis is commonly delayed until late in the disease progression. We present a case of a 77-year-old woman with stage IV metastatic adenocarcinoma of lower GI with mesenteric involvement and pulmonary nodules. Her disease was confirmed by mesenteric mass biopsy and was histologically CK20 positive, CDX positive, and CK7 negative. She underwent eighteen rounds of palliative chemotherapy with oral capecitabine (Xeloda) over the course of fifteen months. Sixteen months after the initial diagnosis, imaging uncovered a new cystic pelvic mass measuring 15x13x12 cm, decreased mesenteric mass, increasing liver lesion, metastasis to the left adrenal gland, and minimal ascites. She has had vaginal bleeding. Patient underwent total abdominal hysterectomy with bilateral salpingo-oophorectomy and small bowel resection by gynecological oncologist. The left ovary was involved by metastatic adenocarcinoma, 15 cm, consistent with small bowel origin. The small bowel resection showed adenocarcinoma, 3.3 cm in size with serosal invasion arising in an adenoma. Patient is planned for chemotherapy with irinotecan in palliation. Our case demonstrates a rare case of small bowel adenocarcinoma later presenting as a Krukenburg tumor.

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Piton, Nicolas. "Optimisation de la prise en charge diagnostique, pronostique et théranostique des carcinomes broncho-pulmonaires humains : des techniques d’imagerie in vivo à la biologie moléculaire. Ligation -dependent RT-PCR : a new specific and low-cost technique to detect ALK, ROS and RET rearrangements in lung adenocarcinoma A new assay for detection of theranostic gene translocations and MET exon 14 skipping in thoracic oncology. One-year perspective routine LD-RT-PCR in 413 newly diagnosed lung tumors STK11 mutations are associated with lower PDL1 expression in lung adenocarcinoma BRAF V600E mutation is not always present as expected ! A case report of lung and thyroid carcinomas A novel method for in vivo imaging of solitary lung nodules using navigational bronchoscopy and confocal laser microendoscopy." Thesis, Normandie, 2019. http://www.theses.fr/2019NORMR119.

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Le carcinome pulmonaire est une affection grave et fréquente dont la prise en charge a été bouleversée ces dernières années, tant sur le plan diagnostique que pronostique ou « théranostique » avec l’avènement des « thérapies ciblées ». Ces dernières permettent une nette amélioration de la survie et du confort des patients éligibles, mais ne sont pas sans compliquer le travail médical, depuis le diagnostic de la maladie jusqu’au suivi régulier du patient, sans oublier le choix des traitements ou les problèmes techniques posés par la multiplication arborescente des altérations moléculaires à rechercher à partir d’un tissu tumoral souvent peu abondant dans ce contexte particulier de l’oncologie thoracique. Ce travail de thèse collige 5 travaux de recherche selon deux angles d’approche : les marqueurs moléculaires pronostiques et « théranostiques » du cancer pulmonaire, et les procédures de diagnostic in vivo de cette pathologie. Le premier axe comporte 4 articles. Les deux premiers concernent l’évaluation d’une nouvelle technique moléculaire, la LD-RT-PCR, dans la détection des translocation géniques du cancer pulmonaire : la première étude est une étude de faisabilité, la deuxième est un travail de validation. Le troisième article explore l’association entre la présence d’une mutation STK11 dans les carcinomes pulmonaires et l’expression de PDL1. Enfin, le quatrième article est une étude de cas illustrant l’importance de l’approche morphologique du cancer pulmonaire. Le second axe est représenté par un travail comparant une technique d’imagerie in vivo par voie endoscopique utilisant la micro-endoscopie confocale par laser avec l’approche microscopique conventionnelle<br>Lung cancer is a serious and frequent condition for which the management strategies have been dramatically modified in recent years, from a diagnostic, prognostic and “theranostic” perspective, most notably with the introduction of “targeted therapies”. The latter have demonstrated dramatic improvement in both quality of life and survival rates of eligible patients, yet consequently highlight new complications in diagnosis, treatment options or technical considerations which can be attributed to the growing number of molecular alterations to be detected from limited tissue samples frequently encountered in thoracic oncology. This work combines 5 different research papers from 2 different angles: prognostic and “theranostic” molecular markers of lung cancer, as well as in vivo diagnostic procedures of lung cancer. The first angle encompasses 4 articles. The first two evaluate a new molecular technique, LD-RT-PCR, to detect gene translocation in lung cancer. The third article explores the association between STK11 mutations in lung cancer and the expression of PDL1. Finally, the fourth article is a case report illustrating the importance of a morphological approach to lung cancer. The second angle compares in vivo imaging techniques by endoscopy using confocal laser microendoscopy alongside a conventional microscopic approach

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Carneiro, Ana Sofia Sampaio. "Case Report: Adult Haemophagocytic Lymphohistiocytosis, with chronic active EBV infection and ocular immune reconstitution inflammatory syndrome." Master's thesis, 2020. https://hdl.handle.net/10216/128255.

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Carneiro, Ana Sofia Sampaio. "Case Report: Adult Haemophagocytic Lymphohistiocytosis, with chronic active EBV infection and ocular immune reconstitution inflammatory syndrome." Dissertação, 2020. https://hdl.handle.net/10216/128255.

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Książki na temat "Ocular oncology and case report"

Oncology: A Case-based Manual (Oxford Medical Publications). Oxford University Press, USA, 1999.

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Lin, Esther Muscari. Advanced Practice in Oncology Nursing : Case Studies. Saunders, 2001.

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9780197682180 and Gary T. Deimling. Cancer Survivors in Later Life. Oxford University PressNew York, 2025. https://doi.org/10.1093/med/9780197682173.001.0001.

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Abstract This book examines a broad range of topics concerning cancer survivorship in later life. Most cancers and half of all malignancies occur in individuals older than 65. As the population ages, it is estimated that this will increase to 70% by 2030. With the recent advances in medical care, people are living longer after cancer treatments, and the number of cancer survivors is projected to reach 19 million in 2024. This book realistically portrays life after cancer among older adults in terms of continuing health and the emotional challenges they face, and the strength, resources, and growth of those who have survived cancer. This book is organized into eight chapters that reflect some of the key themes in psychosocial and medical oncology as well as in geriatric and social gerontology literatures: physical and mental health, stress appraisal, coping and adaptation, survivor, and illness identity, and altered life perspectives. Within each chapter, a conceptual framework identifies its core themes. These are then examined in terms of prominent foundational and recent research published by others other working in cancer survivorship and aging. Our own research at the Cancer Survivors Research Program (CSRP) at Case Western Reserve University in Cleveland Ohio is featured as well. In addition to the quantitative findings, each chapter provides a narrative that draws on the lived experiences of older adult survivors who participated in our research in their own words. We hope that these “lived experiences” of survivors illuminate the statistics we report.

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Części książek na temat "Ocular oncology and case report"

Hoekman, K., J. van Doorn, T. Gloudemans, et al. "Tumour-induced hypoglycaemia: A case report." In The Teaching Cases from Annals of Oncology. Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-011-5456-7_3.

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Benson, J. R., K. Mokbel, and M. Baum. "Management of desmoid tumours including a case report of toremifene." In The Teaching Cases from Annals of Oncology. Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-011-5456-7_29.

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Majima, Akio. "A Case Report of Deuteranopia with Ocular Albinism: A Variant of Forsius-Eriksson Syndrome." In Colour Vision Deficiencies VIII. Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-009-4275-2_48.

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Cuccurullo, Corrado, Luca D’Aniello, and Maria Spano. "Thematic atlas of Italian oncological research: the analysis of public IRCCS." In Proceedings e report. Firenze University Press, 2021. http://dx.doi.org/10.36253/978-88-5518-304-8.22.

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This paper has been developed in the frame of the research project “V:ALERE 2019” focused on Italian public-owned Academic Medical Centers. The main aim of the project is to provide evidence, advice, and remarks to help the agents of the public health system to address the many challenges that they face. In recent years, there is an increasing recognition of the potential value of research evidence as one of the many factors considered by policymakers and practitioners. Even more, in the case of medical science, the analysis of research and its impact is indispensable, in light of its implications for public health. The starting point for mapping a research area is to review the related scientific literature because by synthesizing past research findings, it is possible to effectively use the existing knowledge base and advance lines of future researches. In this sense, bibliometrics becomes useful, by providing a structured analysis to a large body of information, to infer trends over time, themes researched, and to show the “big picture” of extant research. In particular, in this work, we focus our attention on the scientific production of the last 20 years of the Scientific Institutes for Research, Hospitalization, and Healthcare (IRCCS “Istituto di Ricovero e Cura a Carattere Scientifico”) specialized in the oncology research. IRCCS are biomedical institutions of relevant national interest that drive clinical assistance in strong relation to research activities. They are committed to being a benchmark for the whole public health system for both the quality of patient care and the innovation skills in the field of the organization. All the analyses were carried out by using the Bibliometrix, an open-source tool for quantitative research in scientometrics and bibliometrics that includes all the main bibliometric methods of analysis.

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Geissbühler, Antoine, Randolph A. Miller, and William W. Stead. "The clinical spectrum of decision-support in oncology with a case report of a real world system." In Artificial Intelligence in Medicine. Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/bfb0029455.

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Porsche, Sabine, and Shuo Cui. "Project Case: Sino-German Platform for Precision Oncology—Tailor-Made Trainings for Medical Professionals." In Sustainable Aging. Springer Berlin Heidelberg, 2024. http://dx.doi.org/10.1007/978-3-662-69139-7_15.

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AbstractMalignant tumour has been the leading cause of death among disease-related deaths for a decade in China, and the incidence and mortality rate of all types of cancers in China are both higher than the worldwide average level (National Bureau of Statistics of China (2020). Annual data, statistical database. Retrieved from: http://www.stats.gov.cn/english/Statisticaldata/AnnualData/ [06.11.2020].). According to the National Cancer Center, 7.5 people were diagnosed with cancer every minute, and there were 2.338 million cancer deaths in 2015 (National Cancer Centre (2019). National cancer report. Retrieved from: https://www.cn-healthcare.com/article/20190623/content-520594.html. [06.11.2020].). In 2018, the three leading forms of cancer among new cases were lung (18.1 per cent), colorectum (12.2 per cent) and stomach (10.6 per cent) (International Agency for Research on Cancer, WHO (2018). Number of new cases in 2018, both sexes, all ages. Retrieved from: https://gco.iarc.fr/today/data/factsheets/populations/160-china-fact-sheets.pdf [06.11.2020].).

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Marchan, Ed M. "Case report forms." In Translational Radiation Oncology. Elsevier, 2023. http://dx.doi.org/10.1016/b978-0-323-88423-5.00042-x.

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Barry, Susan. "Case Report Form Development." In Oncology Clinical Trials. Springer Publishing Company, 2018. http://dx.doi.org/10.1891/9780826168733.0022.

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Darlan, D. M., M. F. Rozi, and R. H. Saragih. "Cryptosporidium sp. findings in AIDS patients: A case report." In Stem Cell Oncology. CRC Press, 2018. http://dx.doi.org/10.1201/9781351190152-42.

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"7.11 Ocular cANCA-Positive Vasculitis: a Case Report." In Schlaglicht Augenheilkunde: Entzündliche Augenerkrankungen, edited by Gerhard K. Lang, Gabriele E. Lang, Claus Cursiefen, and Arnd Heiligenhaus. Georg Thieme Verlag, 2016. http://dx.doi.org/10.1055/b-0036-135334.

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Streszczenia konferencji na temat "Ocular oncology and case report"

BONEA, Elena, and Ioan HUTU. "SURGICAL KERATECTOMY WITH KERATOPLASTY OF A MELANOMA IN A PERSIAN CAT USING VETRIX EYEQ GRAFT." In 24th SGEM International Multidisciplinary Scientific GeoConference 2024. STEF92 Technology, 2024. https://doi.org/10.5593/sgem2024v/4.2/s19.46.

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An ocular melanoma is a type of cancer that originates from the uncontrolled growth of melanocytes. In cats, melanomas are rare, with diffuse iris melanomas being the most common eye tumors. This case report describes an 8-year-old female Persian cat referred to our clinic for evaluation due to a dark spot extending to the cornea, obscuring vision, and unresponsive to prior drug treatments. Diagnosis was confirmed through histopathological examination of a tissue sample. The present case report details a complex keratectomy surgery performed to remove the melanoma, utilizing an amniotic graft to reconstruct the cornea. Initially, the procedure began as a straightforward keratectomy, but the melanoma's deep and superficial extension into the corneal tissue required filling the surgical gap with several layers of An-vision Vetrix� EyeQ amniotic graft for corneal reconstruction. The surgery was completed by applying a protective An-Bandage lens and suturing the external eye angle to reduce the palpebral fissure for added protection. Postoperatively, Vetrix EyeQ amniotic eye drops, An-HyPro eye gel, and antibiotic drops were administered for one month. The cat was reexamined at 1 week, and again at 1-, 6-, and 12-months post-surgery, with no signs of melanoma recurrence observed during follow-up. Our study demonstrates the feasibility of successfully removing the melanoma without enucleation, provided that proper surgical and postoperative management is applied, leading to favorable visual outcomes.

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MIRANDA, E. G. R., G. ISHAK, D. P. CASTRO, et al. "HEPATOCELLULAR CARCINOMA: CASE REPORT." In ONCOLOGY 2023 International Symposium. Even3, 2025. https://doi.org/10.29327/oncology-2023-international-symposium.1084819.

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MIRANDA, E. G. R., G. ISHAK, D. P. CASTRO, et al. "CASE REPORT: KLATSKIN TUMOR." In ONCOLOGY 2023 International Symposium. Even3, 2025. https://doi.org/10.29327/oncology-2023-international-symposium.1084811.

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FERREIRA, J. M. T., L. V. S. S., D. P. C., et al. "CASE REPORT: HEPATIC METASTASECTOMY IN RECTAL NEOPLASM." In ONCOLOGY 2023 International Symposium. Even3, 2025. https://doi.org/10.29327/oncology-2023-international-symposium.1084809.

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A., P. A., D. P. C., L. V. S. S., et al. "CASE REPORT: GASTRIC ADENOCARCINOMA WITH BRAIN METASTASIS." In ONCOLOGY 2023 International Symposium. Even3, 2025. https://doi.org/10.29327/oncology-2023-international-symposium.1084808.

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HAGE, L. D. S. M., I. G., T. G., I. U. A., P. A. A., and E. S. M. N. "CASE REPORT: SOLID PSEUDOPAPILLARY TUMOR OF THE PANCREAS." In ONCOLOGY 2023 International Symposium. Even3, 2025. https://doi.org/10.29327/oncology-2023-international-symposium.1084800.

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VALENTE, R. B., A. C. PARADELA, M. C. A. COSTA, et al. "PLASMABLASTIC LYMPHOMA IN AN IMMUNOCOMPETENT PATIENT: CASE REPORT." In ONCOLOGY 2023 International Symposium. Even3, 2025. https://doi.org/10.29327/oncology-2023-international-symposium.1084831.

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SOUSA, A. C. C., C. M. A. FERNANDES, A. A. DIAS, and M. A. B. GONÇALVES. "MESONEPHRIC ADENOCARCINOMA OF THE UTERINE CERVIX – A CASE REPORT." In ONCOLOGY 2023 International Symposium. Even3, 2025. https://doi.org/10.29327/oncology-2023-international-symposium.1084823.

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MORATTO, M. A., F. O. OLIVEIRA, N. A. SOARES, et al. "GASTRIC ADENOCARCINOMA AND EPSTEIN-BARR VIRUS: A CASE REPORT." In ONCOLOGY 2023 International Symposium. Even3, 2025. https://doi.org/10.29327/oncology-2023-international-symposium.1084798.

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