2024
Skin Thickening and Vascular Lesions
Andrejeva L, Lanjewar S, Woolf G, Killelea B, Brownson K, Podany P, Harigopal M. Skin Thickening and Vascular Lesions. 2024, 297-323. DOI: 10.1007/978-3-031-65711-5_11.Peer-Reviewed Original ResearchRare group of neoplasmsInflammatory breast carcinomaInvasive lobular carcinomaMalignant vascular tumorsGroup of neoplasmsIll-defined marginsLobular carcinomaBreast carcinomaBenign tumorsClinical presentationBenign lesionsVascular tumorsBreast parenchymaClinical historyWell-circumscribedSkin thickeningMalignant processVascular lesionsRare groupImaging appearanceSubcutaneous tissueContrast enhancementBreastCarcinomaTumor
2023
Vascular steal and associated intratumoral aneurysms in highly vascular brain tumors: illustrative case
Hong C, Marianayagam N, Morales-Valero S, Barak T, Tabor J, O’Brien J, Huttner A, Baehring J, Gunel M, Erson-Omay E, Fulbright R, Matouk C, Moliterno J. Vascular steal and associated intratumoral aneurysms in highly vascular brain tumors: illustrative case. Journal Of Neurosurgery Case Lessons 2023, 5: case22512. PMID: 36880509, PMCID: PMC10550659, DOI: 10.3171/case22512.Peer-Reviewed Original ResearchVascular brain tumorsVascular stealIntratumoral aneurysmBrain tumorsAdditional vascular imagingRight ophthalmic arteryMaximal safe resectionDiagnostic cerebral angiographyMinimal blood lossVascular steal phenomenonOpen tumor resectionDural-based lesionsSteal phenomenonBlood lossCerebral angiographyClinical suspicionNeurological symptomsOphthalmic arterySurgical strategySafe resectionVascular tumorsBlurred visionEndovascular embolizationTomography angiographyTumor resectionUpdate of pediatric bone tumors—other mesenchymal tumors of bone, hematopoietic neoplasms of bone, and WHO classification of undifferentiated small round cell sarcomas of bone
Wang A, Maloney E, Al-Dasuqi K, Irshaid L, Ahmed A, Haims A, Porrino J. Update of pediatric bone tumors—other mesenchymal tumors of bone, hematopoietic neoplasms of bone, and WHO classification of undifferentiated small round cell sarcomas of bone. Skeletal Radiology 2023, 52: 1443-1463. PMID: 36656343, DOI: 10.1007/s00256-023-04286-8.Peer-Reviewed Original ResearchConceptsUndifferentiated small round cell sarcomaSmall round cell sarcomasBone tumorsRound cell sarcomasPediatric populationCell sarcomaMesenchymal tumorsHematopoietic neoplasmsWorld Health Organization classificationGiant cell-rich tumorsPediatric bone tumorsOsteogenic tumorsOrganization classificationVascular tumorsNotochordal tumorsTumorsGenetic sequencing techniquesChondrogenic tumorsCertain lesionsSoft tissueBoneSarcomaNeoplasmsSeparate manuscriptDetailed update
2022
Update of pediatric bone tumors—notochordal tumors, chondrogenic tumors, and vascular tumors of the bone
Lee H, Wang A, Cheng R, Moran J, Al-Dasuqi K, Irshaid L, Maloney E, Porrino J. Update of pediatric bone tumors—notochordal tumors, chondrogenic tumors, and vascular tumors of the bone. Skeletal Radiology 2022, 52: 1101-1117. PMID: 36369290, DOI: 10.1007/s00256-022-04235-x.Peer-Reviewed Original ResearchRare presentation of angiomatosis in the paranasal sinuses mimicking juvenile nasopharyngeal angiofibroma in a 16 year old male
Suresh N, Shah V, Matichak D, Ghiam M, Pasick L, Abecassis I, Saad A, Morcos J, Sargi Z, Bhatia R. Rare presentation of angiomatosis in the paranasal sinuses mimicking juvenile nasopharyngeal angiofibroma in a 16 year old male. Radiology Case Reports 2022, 17: 3527-3534. PMID: 35923345, PMCID: PMC9340122, DOI: 10.1016/j.radcr.2022.07.031.Peer-Reviewed Original ResearchJuvenile nasopharyngeal angiofibromaParanasal sinusesSkull baseRare presentationNasopharyngeal angiofibromaHistory of presentationTertiary care centerBroad differential diagnosisInternal maxillary arteryYear old maleSkull base massAdjacent paranasal sinusesFinal pathologyPreoperative embolizationLateral gazeTransphenoidal resectionClinical outcomesEndoscopic biopsyVisual acuitySurgical interventionVascular tumorsEmergency roomSubjective diplopiaCare centerCavernous sinus
2020
A rare case of pediatric intranasal lobular capillary hemangioma
Schild S, Irizarry R, Plum A. A rare case of pediatric intranasal lobular capillary hemangioma. International Journal Of Otorhinolaryngology And Head And Neck Surgery 2020, 6: 2115-2118. DOI: 10.18203/issn.2454-5929.ijohns20204641.Peer-Reviewed Original ResearchLobular capillary hemangiomaCapillary hemangiomaVascular tumorsNine-year-old maleBenign vascular growthsEndoscopic surgical excisionIntermittent unilateral epistaxisNasal cavity tumorsWide local excisionBony-cartilaginous junctionPediatric vascular tumorsNeck literatureFinal histologyPreoperative embolizationLocal excisionNasal traumaArtery supplySurgical excisionCartilaginous involvementRare entityVascular lesionsUnilateral epistaxisDifferential diagnosisRare caseEffective treatmentSolitary Fibrous Tumor of Pancreas With Unusual Features: A Case Report
Afzal A, Maldonado-Vital M, Khan S, Farooque U, Luo W. Solitary Fibrous Tumor of Pancreas With Unusual Features: A Case Report. Cureus 2020, 12: e10833. PMID: 33173639, PMCID: PMC7647364, DOI: 10.7759/cureus.10833.Peer-Reviewed Original ResearchPancreatic solitary fibrous tumorSolitary fibrous tumorGastrointestinal stromal tumorsFibrous tumorDiagnosis of SFTCommon neuroendocrine tumorMalignant clinical courseCluster of differentiationPotential diagnostic pitfallMajority of SFTsClinical courseBiopsied specimensStromal tumorsImmunohistochemical featuresVascular tumorsCase reportNeuroendocrine tumorsDiagnostic challengeDedifferentiated liposarcomaPathological spectrumAnatomic sitesDiagnostic pitfallsFocal positivityHypercellular areasAtypical features
2019
Angiolymphoid Hyperplasia with Eosinophilia with Clinical Presentation Concerning for Juvenile Temporal Arteritis
Li E, Sinard J, Distefano A, Sohrab M. Angiolymphoid Hyperplasia with Eosinophilia with Clinical Presentation Concerning for Juvenile Temporal Arteritis. Ocular Oncology And Pathology 2019, 6: 25-30. PMID: 32002401, PMCID: PMC6984143, DOI: 10.1159/000500361.Peer-Reviewed Original ResearchJuvenile temporal arteritisTemporal arteritisRare eosinophilic dermatosisMagnetic resonance imagingAngiolymphoid hyperplasiaPreoperative workupClinical presentationEosinophilic dermatosisPediatric populationUnknown etiologyVascular tumorsExcisional biopsyFinal diagnosisMonths durationRecent traumaDoppler ultrasoundRight eyebrowResonance imagingComplete examinationArteritisEosinophiliaHyperplasiaWorkupDiagnosisDuration
2018
Pediatric Congenital Cerebrovascular Anomalies
Goyal P, Mangla R, Gupta S, Malhotra A, Almast J, Sapire J, Kolar B. Pediatric Congenital Cerebrovascular Anomalies. Journal Of Neuroimaging 2018, 29: 165-181. PMID: 30378722, DOI: 10.1111/jon.12575.Peer-Reviewed Original ResearchConceptsVascular malformationsCerebrovascular anomaliesCentral nervous system vascular malformationsMultiple developmental venous anomaliesPersistent carotid-vertebrobasilar anastomosesFamilial associationAssociated vascular malformationCarotid-vertebrobasilar anastomosesDevelopmental venous anomaliesPediatric age groupMultiple cavernous malformationsSturge-Weber syndromeCongenital vascular malformationsHereditary hemorrhagic telangiectasiaArterial anomaliesSinus thrombosisVenous anomaliesVenous malformationsVascular abnormalitiesVascular tumorsVascular lesionsDiverse etiologiesArteriovenous malformationsSystemic conditionsFurther managementA practical diagnostic approach to hepatic masses.
Vyas M, Jain D. A practical diagnostic approach to hepatic masses. Indian Journal Of Pathology And Microbiology 2018, 61: 2-17. PMID: 29567877, DOI: 10.4103/ijpm.ijpm_578_17.Peer-Reviewed Original ResearchConceptsDifferential diagnosisHepatic massCorrect diagnosisRight diagnosisBackground liver diseaseUnknown primary siteFocal nodular hyperplasiaHepatic mass lesionsPractical diagnostic approachList of antibodiesNonhepatocellular originProper workupClinical presentationHepatocellular originLiver diseaseHistologic featuresPrimary lesionClinicopathological correlationHepatic adenomaVascular tumorsMass lesionNonepithelial neoplasmsCommon siteNeedle biopsyNodular hyperplasia
2017
Clinicopathological analysis of ATRX, DAXX and NOTCH receptor expression in angiosarcomas
Panse G, Chrisinger JS, Leung CH, Ingram DR, Khan S, Wani K, Lin H, Lazar AJ, Wang W. Clinicopathological analysis of ATRX, DAXX and NOTCH receptor expression in angiosarcomas. Histopathology 2017, 72: 239-247. PMID: 28796347, DOI: 10.1111/his.13337.Peer-Reviewed Original ResearchMeSH KeywordsAdaptor Proteins, Signal TransducingAdolescentAdultAgedAged, 80 and overBiomarkers, TumorCo-Repressor ProteinsDisease-Free SurvivalFemaleHemangiosarcomaHumansKaplan-Meier EstimateMaleMiddle AgedMolecular ChaperonesNuclear ProteinsPrognosisReceptors, NotchX-linked Nuclear ProteinYoung AdultConceptsNotch2 expressionWorse disease-specific survivalWorse event-free survivalDisease-specific survivalEvent-free survivalMalignant vascular tumorsPoor clinical outcomeATRX lossCase of angiosarcomaDeep soft tissuesPathogenesis of angiosarcomaTumor suppressive roleProtein 6 expressionNotch receptor expressionMental retardation syndrome XMultiple genetic alterationsSite of originInhibition of NotchAdvanced diseaseCutaneous sitesClinical outcomesPrognostic significanceClinicopathological analysisSyndrome XVascular tumors
2016
GNA14 Somatic Mutation Causes Congenital and Sporadic Vascular Tumors by MAPK Activation
Lim YH, Bacchiocchi A, Qiu J, Straub R, Bruckner A, Bercovitch L, Narayan D, Genomics Y, McNiff J, Ko C, Robinson-Bostom L, Antaya R, Halaban R, Choate KA. GNA14 Somatic Mutation Causes Congenital and Sporadic Vascular Tumors by MAPK Activation. American Journal Of Human Genetics 2016, 99: 443-450. PMID: 27476652, PMCID: PMC4974082, DOI: 10.1016/j.ajhg.2016.06.010.Peer-Reviewed Original ResearchMeSH KeywordsCells, CulturedChild, PreschoolEnzyme ActivationGTP-Binding Protein alpha SubunitsGTP-Binding Protein alpha Subunits, Gq-G11Human Umbilical Vein Endothelial CellsHumansInfantInfant, NewbornIntercellular Signaling Peptides and ProteinsMaleMAP Kinase Signaling SystemMelanocytesMitogen-Activated Protein KinasesMutationProto-Oncogene Proteins c-aktVascular NeoplasmsConceptsLobular capillary hemangiomaVascular tumorsKaposiform hemangioendotheliomaMonths of lifeYears of ageSomatic activating mutationsGNA14 mutationsHuman endothelial cellsPharmacologic interventionsSignificant complicationsCommon neoplasmCapillary hemangiomaInfantile hemangiomasLCH lesionsPrimary human endothelial cellsTherapeutic interventionsActivating mutationsGNA11 mutationsTumorsEndothelial cellsLesionsPotential targetHemangiomaGNA14Somatic mutations
2015
Somatic p.T771R KDR (VEGFR2) Mutation Arising in a Sporadic Angioma During Ramucirumab Therapy
Lim YH, Odell ID, Ko CJ, Choate KA. Somatic p.T771R KDR (VEGFR2) Mutation Arising in a Sporadic Angioma During Ramucirumab Therapy. JAMA Dermatology 2015, 151: 1240-1243. PMID: 26422291, DOI: 10.1001/jamadermatol.2015.1925.Peer-Reviewed Original ResearchConceptsVascular endothelial growth factor 2Vascular lesionsRamucirumab therapyNon-small cell lung carcinomaExome sequencingNew vascular lesionsMetastatic rectal cancerCell lung carcinomaRich blood supplySomatic mutationsInhibition of angiogenesisVia exome sequencingPotential adverse effectsRight shinAntiangiogenic therapeuticsGrowth factor 2Rectal cancerCombination therapyVascular tumorsGastric adenocarcinomaHistological featuresLung carcinomaBlood supplyRight legIrinotecan hydrochlorideRenal Cell Carcinoma and Targeted Therapy
Gartrell B, Small A, Oh W, Galsky M. Renal Cell Carcinoma and Targeted Therapy. 2015, 287-295. DOI: 10.1002/9781118468678.ch29.Peer-Reviewed Original ResearchRenal cell carcinomaVascular endothelial growth factor (VEGF)/vascular endothelial growth factor receptorClear-cell renal cell carcinomaResistant to cytotoxic chemotherapyEndothelial growth factor receptorTumor suppressor gene functionEvaluate tumor heterogeneityClear-cell RCCSerum of patientsGrowth factor receptorPathogenesis of renal cell carcinomaMolecular pathogenesis of renal cell carcinomaCytotoxic chemotherapyCell carcinomaVascular tumorsTargeted therapyRenal carcinomaTumor heterogeneityMechanisms of diseaseFactor receptorClinical trialsMolecular pathogenesisVHL diseaseNext-generation sequencingMammalian target
2012
Does a common vascular origin confer similar prognosis to malignant tumors of the liver?
Groeschl R, Pappas S, Christians K, Tsai S, Quebbeman E, Gamblin T, Turaga K. Does a common vascular origin confer similar prognosis to malignant tumors of the liver? Journal Of Clinical Oncology 2012, 30: 186-186. DOI: 10.1200/jco.2012.30.4_suppl.186.Peer-Reviewed Original ResearchMalignant vascular tumorsEpithelioid variantHepatic malignant vascular tumorsOverall survival of patientsAbsence of surgical interventionAnnual standardized incidenceSurvival of patientsAssociated with survivalCox regression modelsStandardized incidence rateMedian survivalSurgical resectionTumor histologyOverall survivalDistant metastasisPrognostic factorsSEER databaseVascular tumorsHepatic hemangiomaShorter survivalSurgical interventionHepatic angiosarcomaMalignant tumorsMetastatic potentialAngiosarcoma
2008
MRI characteristics and classification of peripheral vascular malformations and tumors
Moukaddam H, Pollak J, Haims AH. MRI characteristics and classification of peripheral vascular malformations and tumors. Skeletal Radiology 2008, 38: 535-547. PMID: 19020874, DOI: 10.1007/s00256-008-0609-2.Peer-Reviewed Original ResearchConceptsMagnetic resonance imagingVascular malformationsVascular tumorsPeripheral vascular malformationsCommon vascular tumorSoft tissue massMultiple tissue planesPercutaneous sclerotherapyAnatomic extentSignificant morbidityTransarterial embolizationCongenital hemangiomaMRI characteristicsInfantile hemangiomasTissue massResonance imagingProliferative phaseMain treatmentTissue planesTumorsVital structuresHemangiomaMalformationsSignal voidLesions
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