Search results for "Pathology"

showing 10 items of 8489 documents

Normale und pathologische Reaktionen der Erythrozytenmembran

1963

medicine.medical_specialtyPathologyErythrocyte membraneHematologyMembraneChemistryInternal medicinemedicineAutoantibodyHematologyGeneral MedicinePathologicalBlut Zeitschrift für Blutforschung
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Endoscopic Ultrasonography in the Diagnosis of Regional Lymph Nodes in Esophageal and Gastric Cancer - Results of Studies in Vitro

1993

A total of 90 regional lymph nodes (43 benign/47 metastatic) from 16 surgical resection specimens of patients with esophageal and gastric carcinoma were examined in vitro by endosonography. The validity of endosonographic criteria of lymph node dignity (size, echogenicity, internal echo pattern and margin structure) was assessed using computer-supported B-mode analysis and compared to histopathological results. Of 26 lymph nodes with a diameter of more than 10 mm, 19 were metastatic (72%). The subjective assessment of the internal echo pattern (homogeneity) and the node margins by an experienced observer allowed the diagnosis of metastatic lymph nodes, but there was a high proportion of fal…

medicine.medical_specialtyPathologyEsophageal NeoplasmsEndoscopic ultrasonographyIn Vitro TechniquesSensitivity and SpecificityStomach NeoplasmsHumansMedicineEsophagusLymph nodeUltrasonographybusiness.industryEsophageal diseaseStomachGastroenterologyEchogenicityCancerEndoscopymedicine.diseasemedicine.anatomical_structureLymphatic MetastasisLymph NodesLymphRadiologybusinessEndoscopy
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FOXP2 and language alterations in psychiatric pathology

2019

Background. From the first reports of the linguist Noam Chomsky it has become clear that the development of language has an important genetic component. Several reports in families have shown the relationship between language disorders and genetic polymorphisms. The FOXP2 gene has been a fundamental piece for the understanding of language development. This gene codes for a transcription factor containing a forkhead domain of DNA binding and participates in the regulation of the expression of a large number of genes involved in the embryonic development of fundamental neuronal structures needed for the development of speech and language. Objective. To present an updated view of the relations…

medicine.medical_specialtyPathologyFOXP2 GeneFOXP2030227 psychiatry03 medical and health sciencesPsychiatry and Mental healthClinical PsychologyLanguage development0302 clinical medicineExpression (architecture)Component (UML)medicineNarrative reviewPsychologyPsychiatrySalud mental
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When a death apparently associated to sexual assault is instead a natural death due to idiopathic hypereosinophilic syndrome: The importance of gamma…

2017

We here report a case involving a 21-year-old female, found dead in a central square of a city in the south of Italy. Initial evidences and circumstances were suggestive of a death associated with a sexual assault. Two peripheral blood and two vitreous humor samples were collected for the purpose of gamma-hydroxybutyric acid (GHB) testing from the dead body at two different post-mortem intervals (PMIs): approximately 2 (t0) and 36 (t1) hours. The obtained results showed that, between t0 and t1, there was an increase of GHB concentrations in peripheral blood and vitreous humor of 66.3% and 8.1%, respectively. This case was the first evidence of GHB post mortem production in a dead body and n…

medicine.medical_specialtyPathologyForensic investigationPhysiologyPoison controlHydroxybutyratesAutopsyVitreous humorHypereosinophilic syndrome01 natural sciencesPathology and Forensic Medicine03 medical and health sciencesYoung Adult0302 clinical medicineInternal medicinemedicineEosinophiliaHumans030216 legal & forensic medicineCause of deathHematologyHypereosinophilic syndromebusiness.industry010401 analytical chemistrygamma-Hydroxybutyric acidForensic Medicinemedicine.disease0104 chemical sciencesVitreous BodyIssues ethics and legal aspectsDrug-facilitated sexual assault (DFSA)ItalyRapeFemalesense organsAutopsymedicine.symptomEosinophilic vasculitisbusinessGHBmedicine.drug
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Rare occurrence of Whipple Disease in a young female patient with a fatal outcome

2013

Abstract Whipple Disease is a rare chronic multi-systemic disease caused by the ubiquitous environmental Gram-positive bacterium Tropheryma whipplei . It can be fatal if untreated. Here we describe the fatal outcome in a 27-year-old Caucasian female patient with a three-month history of persistent fever, anemia, weight loss and diarrhea. The final resolution of the diagnostic process was only reached after the patient’s death thanks to autopsy. The case depicted is a classic Whipple Disease histologically characterized by digestive involvement based on positive periodic acid-Schiff (PAS) staining and immunohistochemical analysis for T. whipplei and systemic involvement (pericarditis, brain …

medicine.medical_specialtyPathologyForensic pathologyHealth (social science)AnemiaEpidemiologyAutopsyDiseasePathology and Forensic MedicineForensic pathologyTropheryma whippleiPericarditisSettore MED/43 - Medicina LegalemedicineFat embolismPost-mortem diagnosisbiologybusiness.industryWhipple DiseasePost-mortem diagnosibiology.organism_classificationmedicine.diseaseDermatologyImmunohistochemistryTropheryma whippleibusinessLawWhipple Disease
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Chromoendoscopy in Barrett's oesophagus: is cresyl violet the magic bullet?

2006

The endoscopic detection of Barrett’s epithelium remains challenging even for modern endoscopy. This is mainly due to the fact that Barrett’s epithelium is often patchy and can easily be overlooked by conventional endoscopy with random biopsies. Thus, chromoendoscopy and magnifying endoscopy were introduced to facilitate diagnosis of Barrett’s epithelium and Barrett’s associated neoplasias. Methylene blue-aided chromoendoscopy was firstly introduced by Canto et al. [1]. The authors could show that methylene blue selectively stains specialised columnar epithelium, which is pathognomonic for Barrett’s epithelium. In contrast, dysplastic areas revealed no or weaker staining due to changes in t…

medicine.medical_specialtyPathologyGastroenterologyChromoendoscopyBarrett EsophagusInternal medicineOxazinesmedicineHumansEndoscopy Digestive SystemVillous PatternColoring AgentsHepatologymedicine.diagnostic_testbusiness.industryGastroenterologymedicine.diseaseEpitheliumEndoscopyStainingBenzoxazinesAutofluorescencemedicine.anatomical_structureDysplasiaMagic bulletbusinessDigestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver
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Confocal Laser Endomicroscopy: Technical Advances and Clinical Applications

2010

Since its introduction in 2004, confocal laser endomicroscopy (CLE) has emerged as a valuable tool for gastrointestinal endoscopic imaging. Endomicroscopy enables the endoscopist to obtain real time in vivo histology during ongoing endoscopy thereby creating “optical biopsies.” To date, numerous studies have shown potential applications of endomicroscopy in the clinical setting, including in vivo diagnosis of esophageal squamous cell carcinoma, Barrett’s esophagus, celiac disease, and colonic polyps. Moreover, recent data suggest the potential application of endomicroscopy in the field of molecular imaging. Additionally, in recent months new applications and developments in the field of con…

medicine.medical_specialtyPathologyGastrointestinal DiseasesEndoscopy GastrointestinalFood and drug administrationEndoscopic imagingConfocal imagingPredictive Value of TestsmedicineEndomicroscopyHumansConfocal laser endomicroscopyMicroscopy ConfocalMucous MembraneHepatologymedicine.diagnostic_testbusiness.industryGastroenterologyEquipment DesignWide fieldMolecular ImagingEndoscopyEndoscopes GastrointestinalGastrointestinal TractRadiologyMolecular imagingbusinessGastroenterology
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Surgical pathology and the diagnosis of invasive visceral yeast infection: two case reports and literature review

2013

Invasive mycoses are life-threatening opportunistic infections that have recently emerged as a cause of morbidity and mortality following general and gastrointestinal surgery. Candida species are the main fungal strains of gut flora. Gastrointestinal tract surgery might lead to mucosal disruption and cause Candida spp. to disseminate in the bloodstream. Here we report and discuss the peculiar clinical and morphological presentation of two cases of gastrointestinal Candida albicans lesions in patients who underwent abdominal surgery. Although in the majority of cases reported in the literature, diagnosis was made on the basis of microbiological criteria, we suggest that morphological feature…

medicine.medical_specialtyPathologyGastrointestinal candidaSettore MED/17 - Malattie InfettiveReviewGut floraSettore MED/08 - Anatomia PatologicaSurgical pathologyDiagnosismedicineIn patientSurgical pathologybiologybusiness.industryDiagnosis; Gastrointestinal candidiasis; Surgical pathology; Surgery; Emergency Medicinebiology.organism_classificationSurgical pathology Gastrointestinal candidiasis DiagnosisDermatologyCorpus albicansGastrointestinal candidiasiSettore MED/18 - Chirurgia GeneraleCandida sppEmergency MedicineSurgeryGastrointestinal tract surgeryGastrointestinal candidiasisbusinessAbdominal surgeryDiagnosi
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Aberrant copy numbers of ALK gene is a frequent genetic alteration in neuroblastomas.

2009

A total of 50 neuroblastomas were assessed for frequency of ALK gene copy number aberrations by interphase fluorescence in situ hybridization using a break-apart fluorescence in situ hybridization probe. The data were compared with status of MYCN, 11q, 17q, and 1p36. We observed ALK aberrations (amplification, 1 of 45; gain, 15 of 45 and loss/imbalance, 11 of 45) in a total of 27 (60%) of 45 neuroblastomas. Synchronic MYCN and ALK aberrations accounted for 23 of 45 (51%) tumors; however, MYCN alterations were also detected in 11 (60%) of 18 tumors without ALK aberrations. Our data suggest that copy number aberrations of the ALK gene is a frequent genetic event in the development of neurobla…

medicine.medical_specialtyPathologyGene DosageBiologyPathology and Forensic MedicineNeuroblastomahemic and lymphatic diseasesNeuroblastomamedicineAnaplastic lymphoma kinaseHumansAnaplastic Lymphoma KinaseCopy number aberrationneoplasmsIn Situ Hybridization FluorescenceOncogene ProteinsN-Myc Proto-Oncogene Proteinmedicine.diagnostic_testGenetic AlterationCancerNuclear ProteinsReceptor Protein-Tyrosine KinasesAnatomical pathologyProtein-Tyrosine Kinasesmedicine.diseaseTissue Array AnalysisCancer researchAutonomic neuropathyFluorescence in situ hybridizationHuman pathology
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Syndrome of autosomal recessive polycystic kidneys with skeletal and facial anomalies is not linked to the ARPKD gene locus on chromosome 6p

2000

We report on two sibs, both males, one born at 37 the other at 24 weeks of gestation, both with a syndrome similar to that seen in three sets of sibs by Gillessen-Kaesbach et al. [1993: Am J Med Genet 45:511–518]. Both propositi had polycystic kidneys and hepatic fibrosis indistinguishable from that seen in autosomal recessive polycystic kidney disease (ARPKD), and skeletal and facial anomalies. Skeletal abnormalities included “butterfly” vertebrae, square shape of pelvis, and brachymelia. The facial anomalies included hypertelorism, epicanthic folds, and anteverted nares. Additional external findings were apparently low-set ears and a short neck. Histopathological examination of the kidney…

medicine.medical_specialtyPathologyGenetic heterogeneityBiologyCystic Changemedicine.diseaseAutosomal Recessive Polycystic Kidney DiseaseEndocrinologyGenetic linkageInternal medicinemedicineCystHypertelorismmedicine.symptomGenetics (clinical)Potter SyndromeKidney diseaseAmerican Journal of Medical Genetics
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