Search results for " Cysts"

showing 10 items of 106 documents

Congenital Cystic Lesions of the Bile Ducts: Imaging-Based Diagnosis

2020

Congenital cystic lesions of the bile ducts represent a spectrum of liver and biliary system lesions, resulting from abnormal embryologic development of the ductal plate. These disorders include Caroli disease, choledochal cysts, autosomal dominant polycystic liver disease, congenital hepatic fibrosis, and biliary hamartomas. Each disorder carries a peculiar clinical presentation, prognosis, and risk of complications. Knowledge of radiological findings of fibropolycystic liver diseases is crucial for their appropriate detection and for differential diagnosis with other similar hepatic cystic lesions, in order to avoid relevant misdiagnosis. The aim of this review is to provide an illustrati…

Liver Cirrhosismedicine.medical_specialtyCaroli diseaseDigestive System DiseasesHamartomaCystic lesions030218 nuclear medicine & medical imagingDiagnosis Differential03 medical and health sciencesCystic lesion0302 clinical medicineMedicineHumansRadiology Nuclear Medicine and imagingCholedochal cystsFibropolycystic liver diseasemedicine.diagnostic_testbusiness.industryCystsPolycystic liver diseaseLiver DiseasesUltrasoundGenetic Diseases InbornMagnetic resonance imagingmedicine.diseaseCaroli DiseaseLiver030220 oncology & carcinogenesisCongenital hepatic fibrosisRadiologyDifferential diagnosisbusinessSettore MED/36 - Diagnostica Per Immagini E Radioterapia
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Gray value measurement for the evaluation of local alveolar bone density around impacted maxillary canine teeth using cone beam computed tomography

2021

Background To investigate whether any relationship between local alveolar bone density and maxillary canine impaction using gray values from cone beam computed tomography. Material and Methods The cone beam computed tomography images of 151 patients were retrospectively evaluated. Maxillary canine was defined as an impacted tooth when root formation was complete and the patient’s age older than 13 or the other side of the maxillary canine has completely erupted. Similarly, complete eruption was defined as the tooth in its expected occlusion and position. Using the cone beam computed tomography software, the region of interest which was 5 mm2 in area, was placed in the trabecular bone on cro…

MaleCuspidCone beam computed tomographyBone densitydiagnosisBone DensityOcclusionMaxillaHumansMedicineGeneral DentistryUNESCO:CIENCIAS MÉDICASDental alveolusRetrospective StudiesOrthodonticsOral Medicine and Pathologybusiness.industryImpactionImpacted toothResearchTooth ImpactedMaxillary canineIncreased Bone DensityCone-Beam Computed Tomographynonodontogenic cystsOtorhinolaryngologyFemaleoral cavitySurgeryoral pathologybusinessMedicina Oral Patología Oral y Cirugia Bucal
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Variable phenotype in 17q12 microdeletions: Clinical and molecular characterization of a new case

2014

Microdeletions of 17q12 including the hepatocyte nuclear factor 1 beta (HNF1B) gene, as well as point mutations of this gene, are associated with the Renal Cysts and Diabetes syndrome (RCAD, OMIM 137920) and genitourinary alterations. Also, microdeletions encompassing HNF1B were identified as a cause of Mayer-Rokitansky-Kuster-Hauser Syndrome (MRKH, OMIM 277000) in females and, recently, were associated with intellectual disability, autistic features, cerebral anomaly and facial dysmorphisms. In this report, we describe a boy with a deletion in 17q12 region detected by SNP array, encompassing the HNF1B gene, that showed dysmorphic features, intellectual disability (ID), serious speech delay…

MaleLIM-Homeodomain ProteinsSingle-nucleotide polymorphismHaploinsufficiencyBiologyBioinformaticsPolymorphism Single NucleotideIntellectual DisabilityIntellectual disabilityGeneticsmedicineHumansAbnormalities MultipleLanguage Development DisordersAutistic DisorderChildHNF1B 17q12 SNP array Renal Cysts and Diabetes syndrome Intellectual disabilityHepatocyte Nuclear Factor 1-betaGeneticsHaplotypeForkhead Transcription FactorsGeneral Medicinemedicine.diseaseHNF1BPenetrancePhenotypeHaplotypesSpeech delayFemalemedicine.symptomChromosome DeletionHaploinsufficiencySNP arrayAcetyl-CoA CarboxylaseChromosomes Human Pair 17Transcription Factors
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Microsurgical fenestration of perineural cysts to the thecal sac at the level of the distal dural sleeve

2011

Background Surgery for symptomatic sacral perineural cysts remains an issue of discussion. Assuming micro-communications between the cyst and thecal sac resulting in a valve mechanism and trapping of CSF as a pathomechanism, microsurgical fenestration from the cyst to the thecal sac was performed to achieve free CSF communication. Methods In 13 consecutive patients (10 female, 3 male), MRI revealed sacral perineural cysts and excluded other pathologies. Micro-communication between the thecal sac and the cysts was shown by delayed contrast filling of the cysts on postmyelographic CT. Surgical fenestration achieved free CSF communication between the thecal sac and cysts in all patients. The p…

MaleMicrosurgerymedicine.medical_specialtyTarlov cystendocrine systemCauda EquinaDura matermedicine.medical_treatmentSacral perineural cyst; Tarlov cyst; Meningeal cyst; Meningeal diverticulum; Sacral radiculopathyClinical Neurology610Neurosurgical ProceduresTarlov cyst03 medical and health sciences0302 clinical medicineparasitic diseasesmedicineHumansCyst030212 general & internal medicineSacral perineural cystAgedRetrospective StudiesMeningeal cystClinical Articlemedicine.diagnostic_testbusiness.industryCauda equinaInterventional radiologyMiddle AgedMicrosurgerymedicine.diseasePerineural CystTarlov Cysts3. Good healthSurgeryRadiographymedicine.anatomical_structureFemaleSurgeryDura MaterNeurology (clinical)Thecal sacSpinal Nerve RootsMeningeal diverticulumbusinessMedicine & Public Health; Neurosurgery; Minimally Invasive Surgery; Surgical Orthopedics; Neuroradiology; Neurology; Interventional Radiology030217 neurology & neurosurgerySacral radiculopathyActa Neurochirurgica
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NCAM (CD56) Expression in keratin-producing odontogenic cysts: aberrant expression in KCOT

2015

Background: Keratin-producing odontogenic cysts (KPOCs) are a group of cystic lesions that are often aggressive, with high rates of recurrence and multifocality. KPOCs included orthokeratinised odontogenic cyst (OOC) and parakeratotic odontogenic cysts, which are now considered true tumours denominated keratocystic odontogenic tumours (KCOTs). GLUT1 is a protein transporter that is involved in the active uptake of glucose across cell membranes and that is overexpressed in tumours in close correlation with the proliferation rate and positron emission tomography (PET) imaging results. Methods: A series of 58 keratin-producing odontogenic cysts was evaluated histologically and immunohistochemi…

MalePathologymedicine.medical_specialtyClinical NeurologyOdontogenic TumorsKeratocystsCohort StudiesPathogenesisBasal (phylogenetics)KeratinmedicineHumansCàncerNCAMReceptorNeural Cell Adhesion MoleculesGeneral DentistryRetrospective Studieschemistry.chemical_classificationRegulation of gene expressionOrthokeratinized odontogenic cystDentistry(all)business.industryResearchBiopsy NeedlePrognosisPatologiaImmunohistochemistryGene Expression Regulation NeoplasticKeratocystic odontogenic tumorLogistic Modelsnervous systemOtorhinolaryngologychemistryOdontogenic CystsKeratinsImmunohistochemistryFemaleNeural cell adhesion moleculeKeratocystic Odontogenic TumorNeurology (clinical)Neoplasm Recurrence LocalbusinessSignal TransductionHead & Face Medicine
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Epidemiologic study of odontogenic and non-odontogenic cysts in children and adolescents of a Brazilian population

2017

Background The objective of this study was to describe the frequency of cystic lesions in a Brazilian population of patients histopathologically diagnosed in the first and second decade of life. Material and Methods Retrospective descriptive cross-sectional study was performed. Biopsy records were obtained from the archives of a Brazilian referral center between 1980 and 2016. Results A total of 2.114 biopsy records of pediatric patients were analyzed with oral and maxillofacial lesions. Data such as gender, age, anatomical location, and histopathological diagnosis were collected and categorized. Among all oral and maxillofacial lesions (n=2.114), were diagnosed 294 cases of odontogenic cys…

MalePediatricsEpidemiologic studyCross-sectional study0302 clinical medicineMedicineYoung adultChildeducation.field_of_studyRadicular Cystmedicine.diagnostic_testSoft tissueEpidermoid cystNonodontogenic Cysts:CIENCIAS MÉDICAS [UNESCO]OdontogenicChild Preschool030220 oncology & carcinogenesisUNESCO::CIENCIAS MÉDICASFemaleOral SurgeryBrazilmedicine.medical_specialtyAdolescentPopulationPathology and Forensic MedicineYoung Adult03 medical and health sciencesBiopsyparasitic diseasesHumansRadiology Nuclear Medicine and imagingDentistry (miscellaneous)educationGeneral DentistryRetrospective StudiesOral Medicine and Pathologybusiness.industryResearchInfantRetrospective cohort study030206 dentistrymedicine.diseaseDermatologyEpidemiologic StudiesCross-Sectional StudiesOtorhinolaryngologyOdontogenic CystsBrazilian populationSurgerybusiness
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Orthokeratinized odontogenic cysts: a Spanish tertiary care centre study based on HPV DNA detection

2018

Abstract Background The role of human papillomavirus (HPV) in orthokeratinized odontogenic cysts (OOCs) has rarely been studied. The objective is to describe the clinicopathological findings in a series of OOCs from a Spanish population that were investigated in relation to the possible presence of HPV. Methods A clinicopathological retrospective analysis followed by a molecular analysis of 28 high- and low-risk HPV genotypes was performed in OOC samples of patients seen during the last 15-years in a Spanish tertiary care center. Results Of 115 odontogenic cysts with keratinization, 16 cases of OOCs were confirmed and evaluated. OOCs occurred predominantly in the mandible of males (mean age…

MaleTertiary careCohort StudiesTertiary Care Centers0302 clinical medicineRecurrenceMedicinePapillomaviridaeBiopsy Needlevirus diseasesMiddle AgedImmunohistochemistryfemale genital diseases and pregnancy complicationsOdontogenicMolecular analysisHPV DNA detectionCell Transformation Neoplastic030220 oncology & carcinogenesisCarcinoma Squamous CellOral and maxillofacial surgeryMouth NeoplasmsAdultmedicine.medical_specialtyHPVAdolescentlcsh:Specialties of internal medicineDents MalaltiesRisk AssessmentYoung Adult03 medical and health scienceslcsh:RC581-951HumansMandibular DiseasesNeoplastic transformationGeneral DentistryRetrospective Studiesbusiness.industryOrthokeratinized odontogenic cystResearch030206 dentistryHigh- and low-riskDermatologyOtorhinolaryngologyOtorhinolaryngologySpainDNA ViralOdontogenic CystsEtiologyNeurology (clinical)HPV High- and low-risk Orthokeratinized odontogenic cyst RecurrencebusinessFollow-Up StudiesHead & Face Medicine
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Jaw cysts at children and adolescence : a single-center retrospective study of 152 cases in southern Bulgaria

2010

One hundred fifty two cysts of the upper and lower jaw were examined at patients up to 18 years old treated in the Clinics of Maxillo-Facial Surgery, University Hospital, Plovdiv, Bulgaria for the period 1998 - 2007. Patients were distributed in four age groups (up to 4 years old, from 5 to 9 years old, from 10 to 14 years old, from 15 to 18 years old). Both sexes were constantly affected (52% male, 48% female). The biggest number cystic lesions were found in the third age group (48.7%). The mandible was preferable localization of the lesions (69.7%). Dentigerous cysts predominated (61.8%) - more affected was third age group (31.6%). Radicular cysts were observed two times less (31.6%) - mo…

Malemedicine.medical_specialtyAdolescentJaw CystsOne Hundred FiftySingle CenterCystic lesionAge groupsmedicineHumansBulgariaChildGeneral DentistryRetrospective StudiesSurgical approachbusiness.industryIntraoral approachInfantRetrospective cohort studyUniversity hospital:CIENCIAS MÉDICAS [UNESCO]SurgeryOtorhinolaryngologyChild PreschoolUNESCO::CIENCIAS MÉDICASSurgeryFemalebusiness
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The recurrence of odontogenic keratocysts in pediatric patients is associated with clinical findings of Gorlin-Goltz Syndrome

2019

Background Odontogenic keratocyst (OKC) is an odontogenic developmental cyst that presents distinct clinical behavior. This lesion has been described as dental cysts with keratinization since the 1930s, however the term "OKC" was established in 1956. This study aims to determine the frequency and features of OKC in children aged 0 to 14 years in an oral pathology service in Brazil. Material and Methods A retrospective study was performed to review cases of OKC in children diagnosed between 1986 and 2017. Clinical data were evaluated from medical records (gender, race, age, anatomical location, treatment, radiographic findings and follow-up). Results Ninety-seven cases of OKC were diagnosed …

Malemedicine.medical_specialtyAdolescentmedicine.medical_treatmentBasal Cell Nevus SyndromeAsymptomaticRecurrenceOral and maxillofacial pathologyHumansMedicineKeratocystChildGeneral DentistryRetrospective StudiesOral Medicine and Pathologybusiness.industryResearchInfant NewbornInfantBasal Cell Nevus SyndromeRetrospective cohort study:CIENCIAS MÉDICAS [UNESCO]medicine.diseaseDermatologyCurettagestomatognathic diseasesOtorhinolaryngologyEl NiñoChild PreschoolUNESCO::CIENCIAS MÉDICASOdontogenic CystsFemaleSurgeryNeoplasm Recurrence Localmedicine.symptomDifferential diagnosisbusinessBrazilMedicina Oral Patología Oral y Cirugia Bucal
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A giant fetal urinoma in a neonate without detectable obstructive uropathy

2003

UNLABELLED Fetal urinoma is an uncommon finding in prenatal investigations. Most previous reports have, almost in every case, referred to the presence of an obstructive uropathy and thus to very high pressure in the upper urinary tract during fetal life. In this paper we present a prenatally detected fetal giant urinoma occurring in the absence of an apparent obstructive uropathy but associated with an ipsilateral vesico-ureteral reflux. CASE REPORT A 5-day-old boy, born after a caesarean section in the 37th week of gestation, but without any perinatal distress, came under our observation because of the evidence of a right upper quadrant abdominal mass. This mass had already been detected p…

Malemedicine.medical_specialtyVoiding cystourethrogrammedicine.medical_treatmentFetal urinomaPercutaneous nephrostomySyringoceleUrineurologic and male genital diseasesVesicoureteral refluxNeonateNephrostomy PercutaneouMedicineHumansObstructive uropathyUpper urinary tractNephrostomy PercutaneousUltrasonographymedicine.diagnostic_testFetal urinoma; Neonate; Percutaneous nephrostomy; Syringocele; Vesico-ureteral reflux; Cysts; Drainage; Humans; Infant Newborn; Infant Premature; Male; Nephrostomy Percutaneous; Urine; Pediatrics Perinatology and Child Healthbusiness.industryCystsRefluxInfant NewbornVesico-ureteral refluxmedicine.diseaseUrinomaSurgeryStenosisCystNephrostomyPediatrics Perinatology and Child HealthDrainageSurgerybusinessInfant PrematureHuman
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