Search results for " DIAGNOSIS"

showing 10 items of 1378 documents

Value of videoroscopy in the detection of alterations of  Actinic Cheilitis and the selection of biopsy areas

2015

Background To demonstrate the value of videoroscopy in identifying lesions and alterations not seen by oroscopy and to select the area for biopsy. Material and Methods Eighty patients were subjected to anamnesis, physical exam, videoroscopy exam, toluidine blue test and biopsy. A diagram of the lips was created to record the exact location where the lesion was found. Results Physical exam identified 287 lesions, and videoroscopy identified 587 lesions; erythema and white lesions were the most common lesions associated with actinic cheilitis. Of the 59 performed biopsies, 32 (52.4%) cases were identified by videoroscopy that showed lesions that were not detected during physical examination. …

AdultMalePathologymedicine.medical_specialtyErythemaAdolescentBiopsyVideo RecordingOdontologíaPhysical examinationLesionYoung AdultBiopsyMedicineHumansExact locationOral DiagnosisChildGeneral DentistryAgedAged 80 and overOral Medicine and Pathologymedicine.diagnostic_testbusiness.industryActinic cheilitisResearchDiagnosis OralMiddle Aged:CIENCIAS MÉDICAS [UNESCO]medicine.diseaseCiencias de la saludDermatologyLipOtorhinolaryngologyCheilitisUNESCO::CIENCIAS MÉDICASSurgeryPhysical examFemalemedicine.symptombusinessMedicina Oral, Patología Oral y Cirugía Bucal
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Reversible posterior leukoencephalopathy secondary to indinavir-induced hypertensive crisis: A case report

2002

Reversible posterior leukoencephalopathy syndrome (RPLS) is an uncommon entity related to multiple and different pathologies, the most common being hypertensive crisis. It is believed to be secondary to the breakdown on the blood-brain barrier. At the beginning, it is undistinguishable from other leukoencephalopathies. However, the disappearance of brain lesions after removal of the potential cause, establish the differential diagnosis with other leukoencephalopathies. We present the case of an HIV-infected patient with a RPLS related to a hypertensive crisis short after the initiation of indinavir-containing highly active antiretroviral therapy. Once blood pressure was controlled and indin…

AdultMalePathologymedicine.medical_specialtyHypertensive encephalopathymedicine.medical_treatmentHIV InfectionsIndinavirIndinavirAntiretroviral Therapy Highly ActiveHypertensive EncephalopathyInternal MedicinemedicineHumansChemotherapymedicine.diagnostic_testbusiness.industryProgressive multifocal leukoencephalopathyvirus diseasesMagnetic resonance imagingHIV Protease Inhibitorsmedicine.diseaseMagnetic Resonance ImagingHyperintensityNelfinavirDifferential diagnosisbusinessmedicine.drugAmerican Journal of Hypertension
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Circumscribed palmar or plantar hypokeratosis: a distinctive epidermal malformation of the palms or soles.

2002

Abstract Background: Epidermal malformations of the skin include a group of heterogeneous developmental defects that result from errors in morphogenesis of the epidermis during intrauterine life. Objective: The purpose of this study was to report the clinical and histopathologic features of a distinctive epidermal malformation involving the skin of the palms or soles. Methods: Ten patients were included in this study. All of them showed the same clinical features that consisted of a solitary circumscribed and circular area of erythematous depressed skin on the palm or on the sole. Diagnosis was confirmed by histopathologic study. Results: All patients were middle aged or elderly. Nine patie…

AdultMalePathologymedicine.medical_specialtyKeratosisBowen's DiseaseDermatologySeverity of Illness IndexSampling StudiesLesionDiagnosis DifferentialKeratoderma PalmoplantarmedicineHumansProspective StudiesKeratodermaAgedBowen's diseaseCorneocyteintegumentary systembusiness.industryBiopsy NeedleAnatomyMiddle Agedmedicine.diseaseImmunohistochemistryPorokeratosismedicine.anatomical_structureFemaleEpidermismedicine.symptomDifferential diagnosisEpidermisbusinessPorokeratosisJournal of the American Academy of Dermatology
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Manifestations of the tongue in Neurofibromatosis type 1

2006

Objective:  The aim of this study is to analyse alterations of the tongue and the correlation between these lesions and different types of tumor. Subjects and methods:  A total of 258 cases (131 females, 127 males) of neurofibromatosis type 1 were screened between 1994 and 2004 in our Dermatology Department. All patients included in this study have NF1, as defined by the NIH Consensus Conference. Three cases of neurofibromas of the tongue in patients with neurofibromatosis type were reported. Results:  Our patients showed nodular lesions on the tongue, related to neurofibromas in two patients and plexiform neurofibroma in one patient, respectively. Clinical and hystopatological findings wer…

AdultMalePathologymedicine.medical_specialtyNeurofibromatosis 1Skin NeoplasmsBiopsyMalignancyDiagnosis DifferentialTonguePlexiform neurofibromaTongueBiopsyHumansMedicineNeoplasm InvasivenessNeurofibromatosisGeneral DentistryAgedNeurofibromamedicine.diagnostic_testbusiness.industryCafe-au-Lait SpotsPlexiform neurofibromaConsensus conferenceSoft tissuemedicine.diseaseTongue Neoplasmsmedicine.anatomical_structureOtorhinolaryngologyFemaleDifferential diagnosisbusinessNeurofibromatosis type 1Oral Diseases
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Retrospective analysis of jaw biopsies in young adults. A study of 1599 cases in Southern Brazil

2017

Background To evaluate the prevalence and the characteristics of jaw lesions diagnosed in young adults aged 20 to 30 years in a southern Brazil reference center, over a period of 25 years. And to analyze the concordance between clinical and histological diagnosis. Material and Methods In this cross-sectional retrospective study, the biopsies files from this center were retrieved and data regarding sex, age, bone localization, clinical and histological diagnosis were collected. The histological diagnosis were grouped into the categories Cystic lesions of odontogenic origin, Periapical inflammation, Odontogenic tumors, Bone diseases, Health tissue and Nonspecific diagnostic. Absolute and rela…

AdultMalePathologymedicine.medical_specialtyParadental cystPeriapical cystConcordanceBiopsyPeriapical Granuloma03 medical and health sciencesYoung Adult0302 clinical medicineBiopsymedicinePrevalenceHumansYoung adultGeneral DentistryRetrospective StudiesOral Medicine and Pathologymedicine.diagnostic_testbusiness.industryResearchRetrospective cohort study030206 dentistrymedicine.disease:CIENCIAS MÉDICAS [UNESCO]DermatologyCross-Sectional StudiesOtorhinolaryngology030220 oncology & carcinogenesisUNESCO::CIENCIAS MÉDICASSurgeryFemaleDifferential diagnosisbusinessBrazilJaw Diseases
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Tuberculoid leprosy and Type 1 lepra reaction.

2008

Summary A patient is described with tuberculoid leprosy and Type 1 (lepra) reaction from Sicily a non-endemic region, who lived previously in Manila from 2000 to 2005. The skin lesions became acutely inflamed and edematous. The plaques were painless to touch or pinprick, and there was swelling of the nerves in the fibro-osseous tunnels under the surface of the skin, including both the ulnar nerve at the elbow, and the posterior tibial nerve (medial malleolus). During the course of electro-neurographic studies, conduction velocity in the motory nerves indicated a slowing-down. The diagnosis of leprosy was confirmed by residence in an endemic area for about 5 years, by simultaneous skin lesio…

AdultMalePathologymedicine.medical_specialtyPosterior tibial nerveBiopsyPhilippinesElbowNeural ConductionTuberculoid leprosyLeprostatic AgentsClofazimineNerve conduction velocityDiagnosis DifferentialmedicineHumansUlnar nerveSicilyTravelmedicine.diagnostic_testbusiness.industryPublic Health Environmental and Occupational HealthTuberculoid leprosy Type 1 lepra reaction.medicine.diseaseLeprosy TuberculoidInfectious Diseasesmedicine.anatomical_structureSkin biopsyLeprosyDifferential diagnosisRifampinbusinessDapsone
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Clinicopathologic and immunohistochemical characterization of 14 cases of angioleiomyomas in oral cavity

2018

Background Angioleiomyoma (ALM) is a benign neoplasm that originates from vascular smooth muscle. It is extremely rare in oral cavity. The objective of this study was to evaluate the clinicopathological and immunohistochemical characteristics of all oral angioleiomyomas registered in a Center of Diagnosis of Oral Diseases from 1959 to 2017. Material and Methods Slides from 14 cases of ALM stained with hematoxylin and eosin (H&E) were analyzed to confirm the diagnosis. Moreover, an immunohistochemical panel with alpha-smooth muscle actin (alpha-SMA), desmin, AE1/AE3, CD68, S-100, and CD34 antibodies was performed to evaluate semi-quantitatively the positive cells. Results ALM correspond to 0…

AdultMalePathologymedicine.medical_specialtyTime FactorsH&E stainCD3403 medical and health sciences0302 clinical medicineAngioleiomyomamedicineHumansNeoplasmGeneral DentistryRetrospective StudiesOral Medicine and PathologyCD68business.industryResearch030206 dentistryMiddle Aged:CIENCIAS MÉDICAS [UNESCO]medicine.diseaseImmunohistochemistrystomatognathic diseasesAngiomyomaOtorhinolaryngology030220 oncology & carcinogenesisUNESCO::CIENCIAS MÉDICASImmunohistochemistryFemaleMouth NeoplasmsSurgeryDesminMorphologic diagnosisbusinessMedicina Oral Patología Oral y Cirugia Bucal
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Clinical and histological features of gingival lesions: A 17-year retrospective analysis in a northern Italian population

2012

Objectives: Only few studies on gingival lesions considered large enough populations and contemporary literature does not provide a valid report regarding the epidemiology of gingival lesions within the Italian population. The histopathological and clinical appearance of 538 gingival lesions from northern Italians are described and discussed here. Study Design: The case records of patients referred for the diagnosis and management of gingival lesions, from October 1993 to October 2009, were reviewed. Data regarding the histological type of lesion were also obtained from the biopsy register for each case, and blindly re-examined. Results: We reported a greater frequency of benign lesions (re…

AdultMalePathologymedicine.medical_specialtyTime FactorsHistological analysis2734Clinical appearance; Gingival lesions; Histological analysis; Surgery; Otorhinolaryngology; 2734; Pathology and Forensic Medicine; Dentistry (all)Pathology and Forensic MedicineLesionYoung AdultAdult; Aged; Female; Gingival Diseases; Humans; Italy; Male; Middle Aged; Retrospective Studies; Time Factors; Young AdultBiopsymedicineHumansGeneral DentistryAgedRetrospective StudiesOral Medicine and Pathologymedicine.diagnostic_testbusiness.industryIncidence (epidemiology)Retrospective cohort studyMiddle AgedGingival lesions:CIENCIAS MÉDICAS [UNESCO]medicine.diseaseClinical appearanceDesquamative gingivitisstomatognathic diseasesItalyOtorhinolaryngologyUNESCO::CIENCIAS MÉDICASGingival DiseasesDentistry (all)Research-ArticleFemaleSurgeryOral lichen planusDifferential diagnosismedicine.symptombusinessGingival disease
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Malignant peripheral neuroectodermal tumors in urology.

1995

During the past few years, a new tumor type has emerged in the pediatric and adolescent group of cancer patients, which has been designated malignant peripheral neuroectodermal tumor (MPNT). This tumor has some clinical and pathological signs in common with either soft-tissue sarcomas or classic Ewing's sarcoma, but is defined as a distinct entity because of its immunohistological characteristics. The tumor expresses neuronal markers, but the pattern varies: chromogranin, neuron-specific enolase, synaptophysin, protein S-100 and others. MPNT can occur in the urogenital region. The differential diagnosis on clinical grounds must include Ewing's and soft tissue sarcomas, and also Wilms' tumor…

AdultMalePathologymedicine.medical_specialtyUrologic Neoplasmsbusiness.industryUrologySoft tissue sarcomamedicine.medical_treatmentCancerCombination chemotherapymedicine.diseaseCombined Modality TherapyRadiation therapyFatal OutcomemedicineHumansFemaleSarcomaNeuroectodermal Tumors Primitive PeripheralDifferential diagnosisRadical surgeryNeuroectodermal tumorbusinessChildWorld journal of urology
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Survival of Adults with Acute Lymphoblastic Leukemia in Germany and the United States

2014

BackgroundAdulthood acute lymphoblastic leukemia (ALL) is a rare disease. In contrast to childhood ALL, survival for adults with ALL is poor. Recently, new protocols, including use of pediatric protocols in young adults, have improved survival in clinical trials. Here, we examine population level survival in Germany and the United States (US) to gain insight into the extent to which changes in clinical trials have translated into better survival on the population level.MethodsData were extracted from the Surveillance, Epidemiology, and End Results database in the US and 11 cancer registries in Germany. Patients age 15-69 diagnosed with ALL were included. Period analysis was used to estimate…

AdultMalePediatricsmedicine.medical_specialtyAdolescentNon-Clinical MedicineEpidemiologyScienceLymphoblastic LeukemiaBiostatisticsHematologic Cancers and Related DisordersGermanyLeukemiasEpidemiologyHumansMedicineStatistical MethodsYoung adultSurvival analysisAgedHealth Care PolicyMultidisciplinaryRelative survivalbusiness.industryStatisticsQRCancers and NeoplasmsCancerHematologyMiddle AgedPrecursor Cell Lymphoblastic Leukemia-LymphomaAcute Lymphoblastic Leukemiamedicine.diseaseSurvival AnalysisUnited StatesClinical trialOncologyUnited States ; age groups ; cancer treatment ; German people ; Germany ; cancer detection and diagnosis ; acute lymphoblastic leukemia ; leukemiasMedicineFemaleHealth StatisticsbusinessMathematicsResearch ArticleRare diseasePLoS ONE
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