Search results for "Case Report"

showing 10 items of 771 documents

Retinal detachment with spontaneous dialysis of the ora serrata in a 13-year-old child with neurofibromatosis type 1: a case report.

2020

A 13‑year‑old child diagnosed with neurofibromatosis type 1 who on a routine control presented with rhegmatogenous retinal detachment associated to dialysis of the ora serrata in the left eye (OS). There were no clinical signs or history of contuse ocular trauma. Neurofibromatosis produces alterations in fibroblasts of the cortex of the vitreous base. This results in deficient production of the collagen fibers that anchor the vitreous base to the pars plana and the peripheral neurosensory retina. Thus, suboptimal function of the fibroblasts explains spontaneous avulsion of the vitreous base. Such avulsion in turn is related to dialysis of the ora serrata.

Pars planamedicine.medical_specialtygenetic structuresmedicine.medical_treatmentCase Reportsneurofibromatosis type 1Avulsion03 medical and health sciences0302 clinical medicinelcsh:OphthalmologyOphthalmologyfibroblastsmedicineOra serrataNeurofibromatosisDialysisRetinabusiness.industryrhegmatogenous retinal detachmentRetinal detachmentdialysis of the ora serratamedicine.diseaseeye diseasesvitreous baseOphthalmologymedicine.anatomical_structurelcsh:RE1-994030221 ophthalmology & optometrysense organsbusinessVitreous baseUlls030217 neurology & neurosurgery
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Inverted ductal papilloma of the oral cavity secondary to lower lip trauma. A case report and literature review

2013

Inverted ductal papilloma of the oral cavity is an infrequent benign neoplasm of papillary appearance that originates in the secretory duct of a salivary gland. The etiology is unknown, though some authors have related it to human papillomavirus (HPV) infection. We present the case of a 40-year-old woman with a tumor of the lower lip mucosa. Histopathological study of the lesion diagnosed inverted ductal papilloma of the oral cavity. Human papillomavirus DNA detection and typing based on tumor lesion DNA amplification and posterior hybridization, revealed no presence of viral DNA. The antecedents of trauma reported by the patient could have played an important role in the development of thi…

Pathologymedicine.medical_specialtyAdenomaPapillomavirusesCase ReportOdontologíaLesionMucosa oralIntraductal papillomamedicineotorhinolaryngologic diseasesNeoplasmPapil·lomavirusGeneral DentistryneoplasmsOral Medicine and PathologySalivary glandbusiness.industryvirus diseasesmedicine.disease:CIENCIAS MÉDICAS [UNESCO]Ciencias de la saludstomatognathic diseasesmedicine.anatomical_structureUNESCO::CIENCIAS MÉDICASEtiologyPapillomaOral mucosamedicine.symptombusinessDuct (anatomy)
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Paraneoplastic Focal Outer Retinitis and Optic Neuropathy in a Patient with Small Cell Lung Carcinoma and Anti-CRMP5, Anti-HU and Anti-Amphiphysin An…

2020

Our aim is to describe clinical and optical coherence tomographic features of acute paraneoplastic focal outer retinitis associated with optic neuropathy in a patient diagnosed with small cell lung carcinoma. Bilateral focal outer retinitis, bilateral optic disc oedema and vitritis were identified in a patient with progressive bilateral visual loss and ataxia. Spectral domain optical coherence tomography (SD-OCT) revealed various extents of granular hyperreflectivity and atrophy of the macular outer retinal layers. Serum and cerebrospinal fluid positivity for anti-CRMP5, anti-HU and anti-amphiphysin antibodies intensified the search for an underlying malignancy, and a small cell lung carcin…

Pathologymedicine.medical_specialtyAtaxiagenetic structuresmedicine.medical_treatmentRetinitisCase ReportMalignancy01 natural sciencesOptic neuropathy03 medical and health scienceschemistry.chemical_compound0302 clinical medicineAtrophylcsh:Ophthalmologymedicine0101 mathematicsOptic disc oedemabusiness.industry010102 general mathematicsRetinitisRetinalmedicine.diseaseCollapsin response mediator protein 5eye diseasesRadiation therapyOphthalmologychemistrylcsh:RE1-994030221 ophthalmology & optometryParaneoplastic syndromeAtaxiaSmall Cell Lung Carcinomasense organsmedicine.symptombusinessCase Reports in Ophthalmology
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Primary multifocal anaplastic large cell lymphoma with eyelid involvement: a case report

2019

ABSTRACT Ocular adnexal involvement in CD30+ lymphoproliferative disorders is rare. We report the case of a 73-year-old woman with a relapsing primary cutaneous anaplastic large cell lymphoma on her eyelid. A systemic extension study excluded extracutaneous involvement. Systemic chemotherapy resulted in an optimal response, with complete regression of the cutaneous lesions. There has been no recurrence during the 2 years of follow-up. RESUMO O acometimento ocular adicional nos distúrbios linfoproliferativos CD30+ é raro. Relatamos o caso de uma mulher de 73 anos com linfoma de grandes células anaplásicas primárias recidivantes em sua pálpebra. A avaliação sistêmica excluiu envolvimento extr…

Pathologymedicine.medical_specialtyCD30Neoplasias palpebraisLymphoproliferative disordersPrimary cutaneous anaplastic large cell lymphomalcsh:OphthalmologyComplete regressionmedicineLinfoma anaplásico cutâneo primário de células grandesAnaplastic large-cell lymphomaLymphoma primary cutaneous anaplastic large cellCase reportsRelatos de casosSystemic chemotherapybusiness.industryGeneral MedicineLymphoma T-cell cutaneousEyelid Neoplasmmedicine.diseaseOphthalmologymedicine.anatomical_structurelcsh:RE1-994Linfoma cutâneo de células TEyelidbusinessEyelid neoplasms
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Oral bilateral collagenous fibroma : a previously unreported case and literature review

2018

Collagenous fibroma, also known as desmoplastic fibroblastoma, is a rare benign slow growing tumor particularly uncommon in the oral cavity. The aim of this study was to analyze the clinical and histopathological features of an oral collagenous fibroma as well as to compare this data with those reported in an English-literature review. The thirteenth case of collagenous fibroma in the oral cavity and the first to present clinically as a bilateral mass was described. A 48-years-old female patient was referred to a School of Dentistry, complaining about an asymptomatic swelling on the hard palate, lasting around ten years. The intraoral examination revealed two well-defined mass, bilaterally …

Pathologymedicine.medical_specialtyCD34Connective tissueCase Report03 medical and health sciences0302 clinical medicineBiopsyOral and maxillofacial pathologymedicineGeneral DentistryMouth neoplasmOral Medicine and Pathologymedicine.diagnostic_testbusiness.industry030206 dentistryCollagenous fibromamedicine.disease:CIENCIAS MÉDICAS [UNESCO]stomatognathic diseasesmedicine.anatomical_structure030220 oncology & carcinogenesisUNESCO::CIENCIAS MÉDICASHard palateDifferential diagnosisbusiness
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Primary intraosseous squamous cell carcinoma arising in dentigerous cyst: Report of 2 cases and review of the literature

2015

Dentigerous cysts are one of the most common odontogenic cysts of the oral cavity. Odontogenic cysts can give rise to a variety of neoplasms. Carcinoma arising in a dentigerous cyst is extremely rare, with a review of literature showing near 30 cases. The present report describes 2 cases of primary intraosseous squamous cell carcinoma originated from a dentigerous cyst. The first one refers to a 57-year old female with a persistent lesion in the left retromolarregion and diagnosed with squamous cell carcinoma originated fromthe incomplete excision of the lower third molar follicle during its surgical extraction. The second case describes the case of an 18-year old male with an impacted uppe…

Pathologymedicine.medical_specialtyCancer cellsPrimary Intraosseous Squamous Cell CarcinomaOdontologíaCase ReportQuistosLesionOdontogenic cystCarcinomamedicineGeneral Dentistrybusiness.industrymedicine.disease:CIENCIAS MÉDICAS [UNESCO]Ciencias de la saludDentigerous cystOdontogenicCysts (Pathology)stomatognathic diseasesOdontogenic carcinomaEstudi de casosUNESCO::CIENCIAS MÉDICASCèl·lules cancerosesCase studiesmedicine.symptomDifferential diagnosisOral SurgerybusinessJournal of Clinical and Experimental Dentistry
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A rare case of solitary brain Langerhans cell histiocytosis with intratumoral hemorrhage in a patient affected by Turner syndrome

2016

Background: Langerhans cell histiocytosis (LCH) is a rare disease involving clonal proliferation of cells with characteristics similar to bone marrow-derived Langerhans cells. The case of a young woman, affected by Turner syndrome and a solitary intraparenchymal LCH associated with an osteolytic lesion of the overlying skull, is presented. Case Description: The patient, with an insidious history of headache and a growing soft mass in the left frontal region, presented with a sudden generalized tonic-clonic epileptic seizure. Neuroradiological investigations showed an osteolytic lesion of the left frontal bone and an underlying brain lesion associated with recent signs of bleeding. The patie…

Pathologymedicine.medical_specialtyCase ReportHemorrhageHemorrhage Langerhans cell histiocytosis skull neoplasm03 medical and health sciences0302 clinical medicineLangerhans cell histiocytosisTurner syndromeRare caseMedicineskull neoplasmbusiness.industryPatient affectedLangerhans cell histiocytosiLangerhans cell histiocytosisSkull Neoplasmmedicine.diseaseHemorrhage; Langerhans cell histiocytosis; skull neoplasmOsteolytic lesionSkullmedicine.anatomical_structure030220 oncology & carcinogenesisSurgeryNeurology (clinical)business030217 neurology & neurosurgeryRare diseaseSurgical Neurology International
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Longitudinal 18F-FDG PET and MRI Reveal Evolving Imaging Pathology That Corresponds to Disease Progression in a Patient With ALS-FTD

2019

Single time point positron emission tomography (PET) studies of patients with amyotrophic lateral sclerosis and frontotemporal dementia (ALS-FTD), have demonstrated hypometabolism or hypermetabolism in certain brain regions. To determine whether longitudinal (at baseline and 20.4 months later) PET and magnetic resonance imaging (MRI) reveal evolving brain imaging pathology corresponding to clinical progression in a patient with ALS-FTD, cerebral glucose metabolic rate, cortical thickness (CT) and cortical area (CA) were obtained and symmetric percent change (SPC) for each calculated. The patient had worsening symptoms and signs of bulbar-onset upper motor neuron-predominant ALS as well as l…

Pathologymedicine.medical_specialtyCase ReportLateralization of brain functionlcsh:RC346-429030218 nuclear medicine & medical imagingPrimary progressive aphasia03 medical and health sciences0302 clinical medicineNeuroimagingAphasiaALS-FTDMedicineAmyotrophic lateral sclerosislcsh:Neurology. Diseases of the nervous systemcortical areamedicine.diagnostic_testbusiness.industryMagnetic resonance imagingcortical thicknessmedicine.diseaseaphasiaPETNeurologyNeurology (clinical)medicine.symptombusinessNeurocognitive030217 neurology & neurosurgeryFrontotemporal dementiaMRIFrontiers in Neurology
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Peripheral ameloblastoma of the upper gingiva: Report of a case and literature review

2014

According to the 2005 histological classification of odontogenic neoplasms by the World Health Organization, ameloblastoma is a benign, locally invasive epithelial odontogenic tumor of putative enamel organ origin. There are four distinct subgroups in which this neoplasm can be gathered: the solid/multicystic type, the unicystic type, the desmoplastic and the peripheral type. Peripheral ameloblastoma is believed to be the rarest subgroup, making up for 2 to 10% of all ameloblastomas. From its first description by Kuru in 1911 to date, less than 200 cases of PA have been described in literature. PAs commonly affect the mandible, in the maxilla the most common location is the soft palatal tis…

Pathologymedicine.medical_specialtyCase ReportOdontologíaAmeloblastoma; Oral Disease; Oral surgeryLesionAmeloblastomaOral surgeryPeripheral ameloblastomamedicineAmeloblastomaGeneral DentistryPathologicalOral DiseaseOral Medicine and Pathologybusiness.industryMandibleEnamel organOdontogenic tumormedicine.disease:CIENCIAS MÉDICAS [UNESCO]Ciencias de la saludstomatognathic diseasesMaxillaUNESCO::CIENCIAS MÉDICASmedicine.symptombusiness
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Oral encapsulated vascular malformation: an undescribed presentation in the mouth

2016

Vascular lesions have been classified in two broad categories, hemangiomas and malformations. Encapsulated vascular lesions have not been reported in the oral cavity, but they were described in other sites, mainly in the orbit. Herein, we present a case of an oral encapsulated vascular lesion located in the right buccal mucosa of a 69-year-old male, including histological and immunohistochemical description and a literature review. Key words:Buccal mucosa, hemangioma, vascular malformation, oral cavity.

Pathologymedicine.medical_specialtyCase ReportOdontologíaBioinformaticsOral cavityBuccal mucosaHemangioma03 medical and health sciences0302 clinical medicinemedicineGeneral DentistryOral Medicine and Pathologybusiness.industryVascular malformation030206 dentistryVascular lesionmedicine.disease:CIENCIAS MÉDICAS [UNESCO]Ciencias de la saludeye diseasesstomatognathic diseasesRight buccal mucosamedicine.anatomical_structure030220 oncology & carcinogenesisUNESCO::CIENCIAS MÉDICASsense organsPresentation (obstetrics)businessOrbit (anatomy)
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