Search results for "Differential diagnosis"

showing 10 items of 404 documents

International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency

2016

BACKGROUND: The consensus documents published to date on hereditary angioedema with C1 inhibitor deficiency (C1-INH-HAE) have focused on adult patients. Many of the previous recommendations have not been adapted to pediatric patients. We intended to produce consensus recommendations for the diagnosis and management of pediatric patients with C1-INH-HAE.METHODS: During an expert panel meeting that took place during the 9th C1 Inhibitor Deficiency Workshop in Budapest, 2015 (www.haenet.hu), pediatric data were presented and discussed and a consensus was developed by voting.RESULTS: The symptoms of C1-INH-HAE often present in childhood. Differential diagnosis can be difficult as abdominal pain…

MaleAbdominal painPediatricsdiagnosisComorbidityDiseaseSeverity of Illness IndexEcallantide0302 clinical medicineRisk FactorsDiagnosisImmunology and Allergyheterocyclic compounds030212 general & internal medicineHereditary angioedemaPediatricHereditary Angioedema Types I and IIAge FactorsDisease ManagementCombined Modality TherapyImmunodeficienciesManagementHereditary angioedemaFemaleOriginal ArticleSymptom Assessmentmedicine.symptommanagementAlgorithmsmedicine.drugmedicine.medical_specialtyC1 inhibitor deficiencyImmunology03 medical and health sciencesMeta-Analysis as TopicmedicineHumansMucous MembraneAdult patientsbusiness.industryOriginal ArticlesC1 inhibitor deficiency; Diagnosis; Hereditary angioedema; Management; Pediatric; Immunology and Allergy; Immunologybacterial infections and mycosesmedicine.diseasehereditary angioedemarespiratory tract diseasesClinical trialpediatric030228 respiratory systemC1 inhibitor deficiencyDifferential diagnosisbusinessBiomarkers
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Nonendodontic periapical lesions: a retrospective descriptive study in a Brazilian population

2021

Background Several nonendodontic diseases can occur in the periapical region, resembling endodontic inflammatory conditions. Therefore, the aim of the present study was to determine the frequency of nonendodontic periapical lesions diagnosed in a Brazilian population. Material and Methods The files of two Oral Pathology laboratories were reviewed and all cases including at least one clinical diagnosis of endodontic periapical lesions were selected for the study. After initial selection, demographic and clinical data, clinical diagnosis and final diagnosis were reviewed and tabulated. Final diagnosis included endodontic periapical lesions, and benign and malignant nonendodontic periapical le…

MaleDental practiceDelayed DiagnosisDentistryOdontogenic Tumorswhole exome sequencingAmeloblastomahspa4Oral and maxillofacial pathologyHumansMedicinesomatic mutationGeneral DentistryUNESCO:CIENCIAS MÉDICASRetrospective StudiesPosterior mandibleOral Medicine and PathologyGeneral distributionbusiness.industryResearchmedicine.diseaseOdontogenicOtorhinolaryngologyClinical diagnosisSurgeryBrazilian populationtwo-hit theoryDifferential diagnosisbusinessbrafBrazilMedicina Oral Patología Oral y Cirugia Bucal
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Temporobasal, Transsphenoidal Meningoencephalocele Becoming Symptomatic with Spontaneous Cerebrospinal Fluid Rhinorrhea: Diagnostic Work-up and Micro…

2012

Background  We report the rare case of an adult transsphenoidal meningoencephalocele and outline the microneurosurgical strategy. Clinical history, the findings of computerized tomography (CT) scans and magnetic resonance imaging (MRI), the microsurgical procedure, and histopathology are reported. Case Report  A 54-year-old female patient complained about cerebrospinal fluid (CSF) rhinorrhea; a transnasal biopsy of a mass in the maxillar sinus prior to diagnostic work-up was performed elsewhere. Persisting CSF leakage prompted CT and MRI, which showed brain tissue extending from the left middle cranial fossa into the left sphenoid sinus through several bony defects. The diagnosis of a trans…

MaleMicrosurgerymedicine.medical_specialtyCerebrospinal Fluid RhinorrheaMiddle cranial fossaMeningoceleNeurosurgical Procedures03 medical and health sciences0302 clinical medicineCerebrospinal fluidSphenoid BoneBiopsymedicineHumansSinus (anatomy)Encephalocelerhinorrheamedicine.diagnostic_testbusiness.industryTemporal BoneMagnetic resonance imagingMiddle AgedMagnetic Resonance Imaging3. Good healthSurgeryTreatment Outcomemedicine.anatomical_structure030221 ophthalmology & optometryFemaleSurgeryHistopathologyDura MaterNeurology (clinical)medicine.symptomDifferential diagnosisTomography X-Ray Computedbusiness030217 neurology & neurosurgeryJournal of Neurological Surgery Part A: Central European Neurosurgery
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Multiple sclerosis-like neurological manifestations in a coeliac patient: nothing is as it seems

2012

Cobalamin (vitamin B12) deficiency occurs with several disorders, involving different organs and systems, including blood, bowel, nervous system and eyes. Although the most important features are usually haematological ones, presence of neurological involvement, in the absence of blood count alterations, has just been described in the literature. Here we report the case of a 48-year-old man, suffering from coeliac disease for approximately 5 years, vegetarian, who was admitted to our department, referring dysaesthesia of the left lower limb, decreased libido and erectile dysfunction. Vitamin B12 deficiency was proved, even in the absence of blood count alteration, and treated with a vitamin…

MaleNervous systemmedicine.medical_specialtyMultiple SclerosisSettore MED/09 - Medicina InternaGastroenterologyCobalaminArticleCoeliac diseaseDiagnosis DifferentialMultiple sclerosis; coeliac diseasechemistry.chemical_compoundFolic AcidErectile DysfunctionInternal medicinemedicineHumansMultiple sclerosiParesthesiaVitamin B12business.industryMultiple sclerosisBrainVitamin B 12 DeficiencyGeneral MedicineMiddle Agedmedicine.diseaseMagnetic Resonance ImagingDecreased LibidoSurgeryCeliac DiseaseErectile dysfunctionmedicine.anatomical_structureSpinal CordchemistryVitamin B ComplexDifferential diagnosisbusinesscoeliac disease
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Focal nodular hyperplasia of the liver: an unusual association with diabetes mellitus in a child and review of literature

2010

Abstract Hepatic hemangioma, adenoma and focal nodular hyperplasia are the most frequent benign lesions of the liver, but they are all infrequent among pediatric population. The reports of focal nodular hyperplasia in children have recently increased in number, with many cases associated to drug intake, particularly to chemotherapy. We here describe, to our knowledge, the first case of focal nodular hyperplasia in association with diabetes mellitus in childhood.

MalePathologymedicine.medical_specialtyAdenomamedicine.medical_treatmentBiopsyDiagnosis DifferentialBiliary atresiaDiabetes mellitusBiopsyCase reportmedicineHepatectomyHumansChildChemotherapymedicine.diagnostic_testbusiness.industryFocal nodular hyperplasialcsh:RJ1-570lcsh:Pediatricsmedicine.diseaseDiabetes Mellitus Type 1Focal Nodular HyperplasiaDifferential diagnosisHepatectomybusinessTomography X-Ray ComputedFollow-Up Studies
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Urachal remnants in asymptomatic children: sonographic morphology.

1991

The sonographic morphology of urachal remnants is not well known and findings tend to be misinterpreted. We present urachal remnants in 16 asymptomatic children (1 week-16 years). In the prevesical part two different types of urachal remnants were found: the tubular type with a small outer muscle wall and the fusiform type with a muscle wall thickness up to 12 mm. Further subvariants are presented. Differential diagnosis of the fusiform type includes urachal cyst and tumorous muscle thickening.

MalePathologymedicine.medical_specialtyAdolescentAsymptomaticUrachusReference ValuesmedicineHumansRadiology Nuclear Medicine and imagingChildUrachusUltrasonographybusiness.industrydigestive oral and skin physiologyInfant NewbornInfantAnatomymedicine.diseaseUrachal cystmedicine.anatomical_structureReference valuesChild PreschoolPediatrics Perinatology and Child HealthFemaleThickeningDifferential diagnosisUltrasonographymedicine.symptombusinessWall thicknessPediatric radiology
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Ectopic thymus in the neck; a case report and review of the literature

1987

A soft, poorly defined mass in the right upper neck of a 7-week-old boy was shown on histology to be ectopic thymus. As aberrant thymic tissue often does change into cysts or neoplasms removal is the treatment of choice. Its persistence in the upper neck seems to be very rare. Embryology, incidence, differential diagnosis and treatment are discussed with a review of the literature.

MalePathologymedicine.medical_specialtyEctopic thymusbusiness.industryIncidence (epidemiology)InfantHistologyThymus GlandChoristomamedicine.diseaseThymic TissueOtorhinolaryngologyHead and Neck NeoplasmsEmbryologyMedicineHumansSurgeryDifferential diagnosisbusinessBritish Journal of Plastic Surgery
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Exophthalmos and basilar impression. A contribution to differential diagnosis of endocrine orbitopathy.

1988

We report on a male patient with exophthalmos of unclear etiology, basilar impression, syringohydromyelia and type II Arnold-Chiari malformation. Two diseases involving the orbital region were to be considered in differential diagnostic terms: endocrine orbitopathy and osseous orbit dysplasia. The typical physical appearance associated with basilar impression as well as suppurative keratitis in Lagophthalmos was striking. Tetraspasticity with pareses, bulbar symptoms, proximally pronounced muscular atrophy as well as a left hemihypesthesia was shown neurologically. Although the orbit CT was normal, sonography revealed thickened ocular muscles. There was euthyroidism in diffuse goiter with n…

MalePathologymedicine.medical_specialtyExophthalmosLagophthalmosContext (language use)Endocrine System DiseasesVascular anomalyAutoimmune DiseasesDiagnosis DifferentialAtrophyPlatybasiamedicineOrbital DiseasesExophthalmosHumansbusiness.industryGeneral MedicineMiddle Agedmedicine.diseaseeye diseasesSyringomyeliaArnold-Chiari Malformationmedicine.anatomical_structureDysplasiaSurgerysense organsNeurology (clinical)Differential diagnosismedicine.symptombusinessTomography X-Ray ComputedOrbit (anatomy)Neurosurgical review
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Solitary intraosseous neurofibroma of the mandible. Apropos of a case

2010

Neurofibroma is a benign neoplasm derived from peripheral nerves. Most of these are associated with Neurofibromatosis but may also occur as solitary lesions. When found on the head and neck they are generally located in the soft tissue. Intraosseous location is very rare. The following report describes a case of an intraosseous neurofibroma located in the left mandibular ramus of a 14-year-old child. The patient did not had clinical evidence of the lesion and it was found on a routine radiographic examination. Surgical excision of the lesion was scheduled and the sample was submitted to histopathological study. Representative sample cuts were studied using conventional techniques of hematox…

MalePathologymedicine.medical_specialtyNeurofibromaAdolescentbusiness.industryRadiographyMandibleSoft tissue:CIENCIAS MÉDICAS [UNESCO]medicine.diseaseLesionMandibular NeoplasmsImmunophenotypingOtorhinolaryngologyUNESCO::CIENCIAS MÉDICASmedicineHumansNeurofibromaSurgerymedicine.symptomDifferential diagnosisNeurofibromatosisbusinessGeneral Dentistry
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h-caldesmon immunoreactivity in atypical fibroxanthoma: implications for the differential diagnosis.

2017

MalePathologymedicine.medical_specialtySkin NeoplasmsSkin DiseasesH caldesmonPathology and Forensic MedicineDiagnosis Differential030207 dermatology & venereal diseases03 medical and health sciences0302 clinical medicinemedicineXanthomatosisHumansAgedAged 80 and overHistiocytoma Benign Fibrousbusiness.industryAtypical fibroxanthomamedicine.diseaseImmunohistochemistry030220 oncology & carcinogenesisImmunohistochemistryCalmodulin-Binding ProteinsFemaleDifferential diagnosisbusinessPathology
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