Search results for "Case Report"

showing 10 items of 771 documents

Long-Lasting Cranial Nerve III Palsy as a Presenting Feature of Chronic Inflammatory Demyelinating Polyneuropathy

2015

We describe a patient with chronic inflammatory demyelinating polyneuropathy (CIDP) in which an adduction deficit and ptosis in the left eye presented several years before the polyneuropathy. A 52-year-old man presented with a 14-year history of unremitting diplopia, adduction deficit, and ptosis in the left eye. At the age of 45 a mild bilateral foot drop and impaired sensation in the four limbs appeared, with these symptoms showing a progressive course. The diagnostic workup included EMG/ENG which demonstrated reduced conduction velocity with bilateral and symmetrical sensory and motor involvement. Cerebrospinal fluid studies revealed a cytoalbuminologic dissociation. A prolonged treatmen…

Diplopiamedicine.medical_specialtyWeaknessbusiness.industrylcsh:Rlcsh:MedicineCase ReportChronic inflammatory demyelinating polyneuropathyGeneral Medicinemedicine.diseaseNerve conduction velocitySurgeryCerebrospinal fluidPtosisSensationmedicineSettore MED/26 - Neurologiamedicine.symptombusinessPolyneuropathypolyneuropathy CIDP cranial nervesCase Reports in Medicine
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Successful management of heparin-induced thrombocytopenia using argatroban in a very old woman: a case report.

2012

Thrombosis due to heparin-induced thrombocytopenia (HIT) is rare but has a severe prognosis. Its management is not always easy, particularly in old patients with renal insufficiency. A 95-year-old woman was hospitalized for dyspnea. Curative treatment with unfractionated heparin was started because pulmonary embolism was suspected. Disseminated intravascular coagulation was then suspected because of thrombocytopenia, hypoprothrombinemia, hypofibrinogenemia, and a positive ethanol gelation test. The first immunoassay for HIT was negative. On the 12th day of hospitalization, bilateral cyanosis of the toes occurred associated with recent deep bilateral venous and arterial thrombosis at duplex …

Disseminated intravascular coagulationmedicine.medical_specialtybusiness.industrylcsh:Rlcsh:MedicineCase ReportGeneral MedicineHeparinHypofibrinogenemiamedicine.diseaseThrombosisArgatrobanSurgeryPulmonary embolismHeparin-induced thrombocytopeniamedicineHypoprothrombinemiabusinessmedicine.drugCase reports in medicine
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Mucocele of the dorsal surface of the tongue : a case report

2018

Mucoceles represent one of the most common lesions of the oral cavity, developing as a result of saliva accumulation. The most frequent affected area is the lower lip, followed by floor of mouth, ventral tongue and buccal mucosa. Despite numerous reports of mucoceles originating on the ventral surface of the tongue, only scarce cases of such a lesion identified on the dorsal tongue surface have been described. In this report a mucocele developed on the dorsal tongue of a 74-year-old woman is described. Additionally a review of previously published mucoceles of the dorsal surface of the tongue is provided and discussed. A 74-year-old female patient was referred for a painless swelling on the…

DorsumGranular cell tumorOral Medicine and Pathologymedicine.diagnostic_testbusiness.industryConnective tissueCase Report030206 dentistryAnatomyLingual Thyroid Glandmedicine.disease:CIENCIAS MÉDICAS [UNESCO]Lesion03 medical and health sciences0302 clinical medicinemedicine.anatomical_structureTongue030220 oncology & carcinogenesisUNESCO::CIENCIAS MÉDICASBiopsymedicineMucocelemedicine.symptombusinessGeneral Dentistry
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Q fever: a new ocular manifestation

2011

P Udaondo1,3, S Garcia-Delpech1,2, D Salom1,2, M Garcia-Pous1, M Diaz-Llopis1,21Department of Ophthalmology, Nuevo Hospital Universitario y Politecnico La Fe, Valencia, Spain; 2Faculty of Medicine, Universitat de València, Valencia, Spain; 3Universidad Cardenal Herrera CEU, Valencia, SpainAbstract: Q Fever is a zoonosis caused by Coxiella burnetii. Ocular manifestations are rare in this infection. We describe the case of a man complaining of an intense retro-orbital headache, fever, arthralgia, and bilateral loss of vision, who showed an anterior uveitis accompanied by exudative bilateral inferior retinal detachment and optic disk edema. At the beginning, a Vogt–Koyanag…

Doxycyclineexudative retinal detachmentmedicine.medical_specialtybiologyVkh syndromebusiness.industryPanuveitispanuveitisRetinal detachmentQ feverCase ReportExudative retinal detachmentRE1-994Coxiella burnetiibiology.organism_classificationmedicine.diseaseVogt-Koyanagi-Harada syndromeComplete resolutioneye diseasesOphthalmologyOphthalmologymedicinebusinessQ fevermedicine.drugClinical Ophthalmology
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Necrotizing Soft Tissue Fasciitis after Intramuscular Injection

2018

Necrotizing soft tissue fasciitis (NSTIs) or necrotizing fasciitis is an infrequent and serious infection. Herein, we describe the clinical course of a female patient who received a diagnosis of NSTIs after gluteus intramuscular injection. We also report the results of our review of published papers from 1997 to 2017. Since now, 19 cases of NSTIs following intramuscular injections have been described. We focus on the correlation between intramuscular injection and NSTIs onset, especially in immunosuppressed patients treated with corticosteroids, suffering from chronic diseases or drug addicted. Intramuscular injections can provoke severe tissue trauma, representing local portal of infection…

Drug injectionmedicine.medical_specialtyNecrosisnecrotizing fasciitisbusiness.industryClinical courselcsh:SurgerySoft tissueCase ReportSerious infectionlcsh:RD1-811medicine.diseaseSurgery030207 dermatology & venereal diseases03 medical and health sciences0302 clinical medicineMedicinePharmacology (medical)030212 general & internal medicineRisk factormedicine.symptombusinessIntramuscular injectionFasciitisCase Reports in Surgery
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ECG-gated multislice computed tomography angiography as a comprehensive non-invasive imaging tool in patient with aortic coarctation

2021

We describe a case of a 52-year-old-woman with aortic coarctation demonstrated by means of 40-slice MSCT angiography. Based on the information extracted from MSCT it was possible to display the anatomical configuration of the disease, the thoraco-abdominal collateral pathways. The best therapeutic approach was established on the basis of MSCT findings. MSCT is a reliable and comprehensive tool for the assessment of adult patients with aortic coarctation. (www.actabiomedica.it).

ECG-Gated ScanComputed Tomography AngiographyAngiographyCase ReportCollateralsMiddle AgedCoronary AngiographyAortic CoarctationElectrocardiographyMultidetector Computed TomographyHumansCollateral VascularizationFemaleMultislice Computed Tomography AngiographyActa Bio Medica : Atenei Parmensis
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A novel EDA variant causing X-linked hypohidrotic ectodermal dysplasia: Case report

2021

Abstract Hereditary ectodermal dysplasias are a complex group of inherited disorders characterised by abnormalities in two or more ectodermal derivatives (skin, nails, sweat glands, etc.). There are two main types of these disorders – hidrotic and hypohidrotic/anhidrotic ectodermal dysplasias. Hypohidrotic ectodermal dysplasia (HED) or Christ-Siemens-Touraine syndrome (OMIM: 305100 ) occurs in 1 out of 5000–10,000 births [19] and has an X-linked recessive inheritance pattern (X-linked hypohydrotic ectodermal dysplasia – XLHED) [2] . The main cause of XLHED is a broad range of pathogenic variants in the EDA gene (HGNC:3157, Xq12-13) which encodes the transmembrane protein ectodysplasin-A [4]…

Ectodermal dysplasiaMedicine (General)QH301-705.5Case ReportEctodermal dysplasiaBiologyEndocrinologyR5-920Recessive inheritanceGeneticsmedicineHypohidrotic ectodermal dysplasiaAlleleBiology (General)Molecular BiologyX-linked recessive inheritanceGenetic testingGeneticsmedicine.diagnostic_testPGT-MXLHEDmedicine.diseaseFamily memberChrist-Siemens-Touraine syndromeEctodysplasin AEDAX-linked recessive disorderMolecular Genetics and Metabolism Reports
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Atypical posterior circulation strokes: a case-based review of rare anatomical variations involved

2021

The circle of Willis is a very important vascular mechanism of protecting against cerebral ischemia, especially when circulation within the main arteries irrigating the brain is somehow impeded. As result of congenital malformation arising early in embryonic development, the fetal-type posterior circle of Willis remains as such during the rest of one's life. Consequently, the posterior cerebral artery (PCA) becomes a branch of the internal carotid artery (ICA), rather than of the basilar artery (BA). Furthermore, the rest of collateral circulation, between the anterior and the posterior regions of the brain, is also negatively affected (e.g., leptomeningeal vessels). The anatomical variant …

EmbryologyThalamusCase ReportPosterior cerebral arteryanatomic variantArtery of PercheronMagnetic resonance angiographyPathology and Forensic Medicineartery of Percheronmedicine.arterymedicineBasilar arteryHumanscircle of WillisRetrospective StudiesPosterior Cerebral Arterymedicine.diagnostic_testbusiness.industryCell BiologyGeneral MedicineAnatomyCollateral circulationstrokemedicine.anatomical_structureCerebrovascular CirculationInternal carotid arterybusinessCarotid Artery InternalMagnetic Resonance AngiographyDevelopmental BiologyCircle of WillisMRIRomanian Journal of Morphology and Embryology
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Chameleonic appearance of caseous calcification of the mitral valve – still a problem for its appropriate management

2021

According to the research literature, the caseous calcification of the mitral annulus (CCMA) is a rare variant of the mitral annulus calcification (MAC) entity, described mostly in elderly women. The aim of this study was to present the case of a 53-year-old female patient with caseous calcification of the mitral valve annulus and posterior cusp, which was diagnosed as papillary fibroelastoma. An echo-dense and quasi-homogeneous tumoral mass, measuring 1.6/1.4 cm, at the level of the posterior mitral ring was detected by echocardiographic examination, as well as by cardiac magnetic resonance imaging (MRI). Histopathological analysis revealed fibrous connective tissue with myxoid areas, hyal…

Embryologymedicine.medical_specialtyHeart Valve DiseasesCase ReportPathology and Forensic Medicinemitral calcificationCardiac magnetic resonance imagingMitral valvemedicineAnimalsHumanscaseous calcificationMitral Valve Annuluscardiovascular diseasesMitral annulusmedicine.diagnostic_testbusiness.industrymitral annulusCell BiologyGeneral MedicineMiddle Agedmedicine.diseaseFibrous connective tissuemyxoid structuremedicine.anatomical_structurePapillary fibroelastomacardiovascular systemMitral ValveFemaleRadiologyDifferential diagnosisbusinessDevelopmental BiologyCalcificationRomanian Journal of Morphology and Embryology
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The use of spiral CT in the detection and management of a permanent maxillary first molar with single root and single canal : a rare occurrence

2017

A sound knowledge of the normal tooth morphology and its numerous variations is essential to the success of endodontic therapy. While extra canals and lateral canals are routinely encountered and documented, there also exists the rare possibility of a fewer number of canals than normal. Early detection of such an occurrence is critical to the prevention of iatrogenic errors during endodontic treatment. The advent of spiral CT as a diagnostic tool serves as a much needed confirmation to understand the complex three dimensional anatomy of teeth. The aim of this case report is to highlight one such case reporting unusual morphology of the permanent maxillary first molar displaying single canal…

Endodontic therapyOrthodonticsbusiness.industryDentistryEarly detectionCase Report:CIENCIAS MÉDICAS [UNESCO]Tooth morphologyOperative Dentistry and EndodonticsUNESCO::CIENCIAS MÉDICASMaxillary first molarotorhinolaryngologic diseasesMedicineThree dimensional anatomysense organsbusinessRoot canal anatomySpiral ctGeneral DentistrySpiral
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