2025
Mixed Gestational Trophoblastic Tumors
Hui P. Mixed Gestational Trophoblastic Tumors. 2025, 185-191. DOI: 10.1007/978-3-031-83545-2_12.Peer-Reviewed Original ResearchGestational trophoblastic tumorsEpithelioid trophoblastic tumorGestational trophoblastic neoplasiaTrophoblastic tumorElevated serum hCG levelsSerum hCG levelsAntecedent pregnancyTrophoblastic neoplasiaVaginal bleedingTumor presentationHCG levelsPresenting symptomsRare formDiagnostic considerationsReproductive ageTumorPresentationGestationBleedingPregnancyInterval timeNeoplasiaPatientsCasesDiagnosisEndovascular Embolization versus Observation of Congenital Renal Arteriovenous Malformations: A Retrospective Study
Hufnagle J, Fish A, Schlachter T. Endovascular Embolization versus Observation of Congenital Renal Arteriovenous Malformations: A Retrospective Study. Journal Of Vascular And Interventional Radiology 2025, 36: 988-993.e1. PMID: 39938714, DOI: 10.1016/j.jvir.2025.02.001.Peer-Reviewed Original ResearchCongenital renal arteriovenous malformationRenal arteriovenous malformationType I AVMArteriovenous malformationsEndovascular embolizationAdverse eventsImaging review of patientsReview of patientsArteriovenous malformation ruptureFollow-up dataYakes classificationTransarterial embolizationEmbolization groupPresenting symptomsPatient demographicsRetrospective studyProcedural imagingImaging reviewEmbolizationPatientsObservation groupMalformationsComplicationsVessel sizeNephrectomy
2024
Hybrid aorto-iliac reconstruction for acute infrarenal aortic occlusion: A case report.
Loh S, Aboian E. Hybrid aorto-iliac reconstruction for acute infrarenal aortic occlusion: A case report. Vascular 2024, 17085381241273272. PMID: 39142331, DOI: 10.1177/17085381241273272.Peer-Reviewed Original ResearchAcute aortic occlusionAcute infrarenal aortic occlusionInfrarenal aortic occlusionAortic occlusionAorto-iliac reconstructionStent graftOpen thrombectomyChronic aorto-iliac occlusive diseasePost-operative day 3Lower extremity painArtery stent graftAorto-iliac occlusive diseaseEndovascular balloon occlusionBilateral iliac artery stentsIliac artery stentingDistal embolic protectionExtremity painPresenting symptomsBalloon occlusionCase reportOpen bypassFemoral cutdownFollow-upOpen revascularizationArtery stentingLamotrigine Emerging as a Driver of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis: An 8-Year Retrospective Study
Glahn J, Almeida M, Kochen A, Noel O, Stogner V, Hsia H, Savetamal A. Lamotrigine Emerging as a Driver of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis: An 8-Year Retrospective Study. Burns 2024, 50: 2114-2123. PMID: 39127578, DOI: 10.1016/j.burns.2024.07.006.Peer-Reviewed Original ResearchStevens-Johnson syndromeToxic epidermal necrolysisOff-label useEpidermal necrolysisCause of SJS/TENDiagnosis of SJS/TENBurn centerNon-bipolar mood disordersImpact clinical courseLength of stayBiopsy confirmationDesquamating rashRegional burn centerCausative drugsClinical coursePresenting symptomsClinical presentationSJS/TEN patientsPrescribed lamotriginePatient demographicsHospital courseRetrospective cohortStevens-JohnsonSevere manifestationsPatient populationPresenting clinical and imaging features of patients with clinically amyopathic interstitial lung disease associated with myositis-specific autoantibodies
Tzilas V, Tzouvelekis A, Sotiropoulou V, Panopoulos S, Bouros E, Avdoula E, Ryu J, Bouros D. Presenting clinical and imaging features of patients with clinically amyopathic interstitial lung disease associated with myositis-specific autoantibodies. Frontiers In Medicine 2024, 11: 1392659. PMID: 38711778, PMCID: PMC11070581, DOI: 10.3389/fmed.2024.1392659.Peer-Reviewed Original ResearchMyositis-specific autoantibodiesPresence of myositis-specific autoantibodiesImaging features of patientsChest imaging studiesIdiopathic inflammatory myopathiesFeatures of patientsInterstitial lung diseaseIncreased CK levelsSignificant diagnostic challengeMedian DLCOMedian FVCHRCT patternGottron's papulesUIP patternMedian agePresenting symptomsLung involvementInflammatory myopathiesRadiological featuresDiagnostic challengeMuscle involvementInspiratory cracklesRaynaud's phenomenonComputer-assisted searchLung diseaseComparative analysis of patients with new onset refractory status epilepticus preceded by fever (febrile infection‐related epilepsy syndrome) versus without prior fever: An interim analysis
Jimenez A, Gopaul M, Asbell H, Aydemir S, Basha M, Batra A, Damien C, Day G, Eka O, Eschbach K, Fatima S, Fields M, Foreman B, Gerard E, Gofton T, Haider H, Hantus S, Hocker S, Jongeling A, Aparicio M, Kandula P, Kang P, Kazazian K, Kellogg M, Kim M, Lee J, Marcuse L, McGraw C, Mohamed W, Orozco J, Pimentel C, Punia V, Ramirez A, Steriade C, Struck A, Taraschenko O, Treister A, Yoo J, Zafar S, Zhou D, Zutshi D, Gaspard N, Hirsch L, Hanin A. Comparative analysis of patients with new onset refractory status epilepticus preceded by fever (febrile infection‐related epilepsy syndrome) versus without prior fever: An interim analysis. Epilepsia 2024, 65: e87-e96. PMID: 38625055, DOI: 10.1111/epi.17988.Peer-Reviewed Original ResearchFebrile infection-related epilepsy syndromeRefractory status epilepticusMacrophage inflammatory protein-1 alphaOnset refractory status epilepticusStatus epilepticusCerebrospinal fluidFIRES patientsCerebrospinal fluid interleukin-6Magnetic resonance imaging findingsComparative analysis of patientsAnalysis of patientsChemokine ligand 2Presenting symptomsFebrile infectionsClinical featuresGastrointestinal prodromeImaging findingsInflammatory biomarkersAntiseizure medicationsInterleukin-6Epilepsy syndromesInterim analysisPatientsEpilepticusFever
2023
Seizure as Presenting Symptom of Multisystem Inflammatory Syndrome in Children
D’Ambrosio E, Gauguet S, Miller C, McMahon E, Driscoll C, Mohanty M, Guggina T. Seizure as Presenting Symptom of Multisystem Inflammatory Syndrome in Children. Case Reports In Infectious Diseases 2023, 2023: 3581310. PMID: 37456213, PMCID: PMC10349669, DOI: 10.1155/2023/3581310.Peer-Reviewed Original ResearchMIS-CMultisystem inflammatory syndromeNew-onset seizuresPresenting symptomsInflammatory syndromeDiagnosis of multisystem inflammatory syndromeSevere cardiac dysfunctionCoronary artery dilationCardiac dysfunctionClinical entityCase reportNeurological involvementArtery dilationCOVID-19 infectionClinical pictureFebrile seizuresMedical literatureSeizuresSARS-CoV-2Disease processSyndromeFeverDiagnosisChildhood illnessesSymptoms
2021
Variable Clinical Presentation of Children With Hereditary Hypophosphatemic Rickets With Hypercalciuria: A Case Series
Christensen S, Tebben P, Sas D, Creo A. Variable Clinical Presentation of Children With Hereditary Hypophosphatemic Rickets With Hypercalciuria: A Case Series. Journal Of The Endocrine Society 2021, 5: a708-a708. PMCID: PMC8090272, DOI: 10.1210/jendso/bvab048.1442.Peer-Reviewed Original ResearchYear old maleYear old femaleHereditary hypophosphatemic ricketsHypophosphatemic ricketsDihydroxyvitamin DSerum phosphorusPhosphate wastingVitamin DElevated 1,25-dihydroxyvitamin DRecurrent urinary stonesLower extremity painVariable clinical presentationLow serum phosphorusPatellofemoral pain syndromePhenotype-genotype correlationProximal renal tubular cellsRenal tubular cellsSLC34A3 geneRenal ultrasoundUrine phosphorusExtremity painPain syndromePresenting symptomsUrine phosphateBone symptoms
2019
Differentiation syndrome in acute promyelocytic leukaemia
Stahl M, Tallman M. Differentiation syndrome in acute promyelocytic leukaemia. British Journal Of Haematology 2019, 187: 157-162. PMID: 31410848, DOI: 10.1111/bjh.16151.Peer-Reviewed Original ResearchConceptsAll-trans retinoic acidDifferentiation syndromeAcute promyelocytic leukemia differentiation syndromeArsenic trioxideAcute renal failureTreated with all-trans retinoic acidAcute promyelocytic leukemiaSteroid prophylaxisUnexplained hypotensionPulmonary infiltratesClinical suspicionUnexplained feverPresenting symptomsPericardial effusionProphylaxis strategiesRenal failureImmediate treatmentSevere casesPromyelocytic leukemiaProphylaxisClinical signsRetinoic acidSyndromeSteroidsAPL
2016
Esophageal adenocarcinoma and squamous cell carcinoma in children and adolescents: Report of 3 cases and comprehensive literature review
Theilen T, Chou A, Klimstra D, LaQuaglia M. Esophageal adenocarcinoma and squamous cell carcinoma in children and adolescents: Report of 3 cases and comprehensive literature review. Journal Of Pediatric Surgery Case Reports 2016, 5: 23-29. PMID: 27057484, PMCID: PMC4819333, DOI: 10.1016/j.epsc.2015.12.008.Peer-Reviewed Original ResearchSquamous cell carcinomaCell carcinomaEsophageal adenocarcinomaPatients treated with surgeryCases of esophageal adenocarcinomaMalignant esophageal tumorsHistory of dysphagiaCases of SCCYears of ageCases of ACMetastatic diseaseEsophageal tumorsAC tumorsPresenting symptomsSCC tumorsGastroesophageal junctionMale predominanceMalignant diseasePatient demographicsYounger patientsDistal esophagusClinical deteriorationAdenocarcinomaDisease characteristicsTumor
2014
Impact of Glanzmann’s Thrombasthenia (GT): Perceptions from US Patients and Parents
Recht M, Rajpurkar M, Chitlur M, Reding M, Frey M, Peltier S, Guelcher C, Stephens D, Cooper D. Impact of Glanzmann’s Thrombasthenia (GT): Perceptions from US Patients and Parents. Blood 2014, 124: 4853. DOI: 10.1182/blood.v124.21.4853.4853.Peer-Reviewed Original ResearchGlanzmann's thrombastheniaMucocutaneous bleedingPlatelet transfusionsAdult patientsAbnormal menstrual cyclesFrequent presenting symptomGlycoprotein IIb/IIIa expressionBleeding disorders populationSevere mucocutaneous bleedingIIb/IIIa expressionParents of affected childrenHematology referralsPresenting symptomsDefinitive diagnosisMenstrual cyclePrevent bleedingUS patientsBleedingImmediate treatmentPatientsHematologistsTransfusionConfirmatory testPlateletThrombasthenia
2000
Carcinoid Tumors of the Extrahepatic Bile Ducts
Maitra A, Krueger J, Tascilar M, Offerhaus G, Angeles–Angeles A, Klimstra D, Hruban R, Albores–Saavedra J. Carcinoid Tumors of the Extrahepatic Bile Ducts. The American Journal Of Surgical Pathology 2000, 24: 1501-1510. PMID: 11075851, DOI: 10.1097/00000478-200011000-00005.Peer-Reviewed Original ResearchMeSH KeywordsAdultAgedBile Duct NeoplasmsBile Ducts, ExtrahepaticCarcinoid TumorChromograninsCytoplasmic GranulesDNA, NeoplasmDNA-Binding ProteinsFemaleFollow-Up StudiesGastrinsHumansImmunoenzyme TechniquesLoss of HeterozygosityLymph NodesLymphatic MetastasisMicrosatellite RepeatsMiddle AgedNeurosecretory SystemsPancreatic PolypeptidePancreaticoduodenectomySerotoninSmad4 ProteinSomatostatinSynaptophysinTrans-ActivatorsTreatment OutcomeConceptsExtrahepatic bile ductCarcinoid tumorsBile ductPresence of lymph node metastasisLoss of heterozygosity analysisCodon 12 of K-rasDisease free 2Low malignant potentialLymph node metastasisPancreatic polypeptideRound neurosecretory granulesPeptic ulcer diseaseIndolent coursePainless jaundiceExpressed synaptophysinP53 mutationsPresenting symptomsMalignant potentialDpc4 proteinNode metastasisObstructive jaundiceGranular chromatinSegmental resectionEndocrine manifestationsP53 loss
1998
THE RIGID FLATFOOT Tarsal Coalitions
Blakemore L, Cooperman D, Thompson G. THE RIGID FLATFOOT Tarsal Coalitions. Foot And Ankle Clinics 1998, 3: 609-631. DOI: 10.1016/s1083-7515(24)00063-9.Peer-Reviewed Original ResearchRigid flatfoot deformityCartilaginous coalitionTarsal coalitionCalcaneonavicular coalitionFlatfoot deformityOnset of symptomsPlain radiographsTalocalcanealSymptomatic recurrenceOperative treatmentPresenting symptomsSurgical treatmentComputerized tomographyMesenchymal differentiationDegenerative changesChildrenSymptomsPatientsMultiple coalitionsArthrodesisPainTreatmentTiming of ossificationAdolescents
1995
A Clinicopathologic Study of 28 Cases
Klimstra D, Moran C, Perino G, Koss M, Rosai J. A Clinicopathologic Study of 28 Cases. The American Journal Of Surgical Pathology 1995, 19: 782-791. PMID: 7793476, DOI: 10.1097/00000478-199507000-00006.Peer-Reviewed Original ResearchConceptsFocal myxoid areasMature-appearing lymphocytesHigh-grade tumorsLow-grade tumorsRoutine chest radiographyWell-differentiated tumorsClinical follow-upRecurrent tumorsAggressive courseChest painMediastinal liposarcomaLymphoid neoplasmsMyxoid subtypeFibroinflammatory conditionMyxoid tumorsPresenting symptomsSclerosing subtypeChest radiographyResidual thymusThymic tissuePlasma cellsPleomorphic typeFollow-upLipoma-likeMyxoid areas
1992
Acinar Cell Carcinoma of the Pancreas
Klimstra D, Heffess C, Oertel J, Rosai J. Acinar Cell Carcinoma of the Pancreas. The American Journal Of Surgical Pathology 1992, 16: 815-837. PMID: 1384374, DOI: 10.1097/00000478-199209000-00001.Peer-Reviewed Original ResearchConceptsAcinar cell carcinomaCell carcinomaIncreased serum lipase levelsCase of acinar cell carcinomaSerum lipase levelsRegional lymph nodesZymogen-like granulesFollow-up informationDiastase-resistant cytoplasmic granulesMetastatic diseaseMinimal pleomorphismHistological subtypesDesmoplastic stromaPresenting symptomsClinical behaviorIndividual tumorsInfluence prognosisLymph nodesSolid tumorsAdult patientsImmunohistochemical staining propertiesLipase levelsScanty cytoplasmFollow-upPleomorphic electron-dense granules
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