2022
Considerations in the management of hereditary angioedema due to C1-INH deficiency in women of childbearing age
Hsu FI, Lumry W, Riedl M, Tachdjian R. Considerations in the management of hereditary angioedema due to C1-INH deficiency in women of childbearing age. Allergy, Asthma & Clinical Immunology 2022, 18: 64. PMID: 35831891, PMCID: PMC9281160, DOI: 10.1186/s13223-022-00689-9.Peer-Reviewed Reviews, Practice Guidelines, Standards, and Consensus StatementsHereditary angioedemaHealth statusAdverse fetal outcomesCohort of patientsChoice of therapyContinuity of careMedical Advisory BoardC1-INH deficiencyWomen's health statusRisk-benefit assessmentHAE attacksHAE managementFetal outcomesProphylactic therapyPatient populationTreatment optionsFemale sexDisease burdenTreatment decisionsContraceptive useUnpredictable episodesTreatment efficacyMucous membranesGynecologic specialistsPregnancy
2020
Pathologies of oral and sinonasal mucosa following facial vascularized composite allotransplantation
Kauke-Navarro M, Tchiloemba B, Haug V, Kollar B, Diehm Y, Safi AF, Treister NS, Annino DJ, Marty FM, Lian CG, Murphy GF, Pomahac B. Pathologies of oral and sinonasal mucosa following facial vascularized composite allotransplantation. Journal Of Plastic Reconstructive & Aesthetic Surgery 2020, 74: 1562-1571. PMID: 33376080, DOI: 10.1016/j.bjps.2020.11.028.Peer-Reviewed Original ResearchConceptsNasal mucous membraneMucous membranesMucosal inflammationMucosal lesionsBanff gradeInflammatory mucosal lesionsUlceration/erosionRetrospective cohort studyClinico-pathologic variablesMucosal rejectionCohort studyCutaneous changesIndependent predictorsMucosal assessmentOral lesionsSkin rejectionSinonasal mucosaCommon lesionsMedical recordsUnivariate analysisCutaneous pathologyBuccal mucosaNasal vestibuleOral cavityComposite allotransplantation
2013
Esophageal stricture secondary to drug-induced toxic epidermal necrolysis presenting in an adult: an unusual complication of a rare disease.
Njei B, Schoenfeld A, Vaziri H. Esophageal stricture secondary to drug-induced toxic epidermal necrolysis presenting in an adult: an unusual complication of a rare disease. Connecticut Medicine 2013, 77: 541-4. PMID: 24273804.Peer-Reviewed Original ResearchConceptsToxic epidermal necrolysisAllopurinol-induced toxic epidermal necrolysisEsophageal strictureEpidermal necrolysisDrug-induced toxic epidermal necrolysisPercutaneous endoscopic gastrostomy feeding tubePercutaneous endoscopic gastrostomy siteEsophageal dilatation proceduresProximal esophageal strictureLife-threatening skin diseaseAdult patientsGastrostomy feeding tubeTriamcinolone acetonideWidespread inflammationDilation proceduresGastrostomy siteRare diseaseRegular dietEsophageal lumenUltrasound endoscopyPatientsEndoscopyFeeding tubeMucous membranesRare situationSystemic retinoids in the management of ichthyoses and related skin types
DiGiovanna JJ, Mauro T, Milstone LM, Schmuth M, Toro JR. Systemic retinoids in the management of ichthyoses and related skin types. Dermatologic Therapy 2013, 26: 26-38. PMID: 23384018, PMCID: PMC3884695, DOI: 10.1111/j.1529-8019.2012.01527.x.Peer-Reviewed Reviews, Practice Guidelines, Standards, and Consensus StatementsConceptsSkin typeHigh-dose vitaminMainstay of therapyTeratogenic side effectsSystemic retinoidsTerm retinoidsCareful surveillanceLimit toxicityEffective therapyDemonstrated efficacySide effectsMucous membranesVitamin ASevere ichthyosisSynthetic retinoidsEarly useRetinoidsTherapyVariety of agesSynthetic derivativesEfficacyTreatmentLimited usefulnessAcetretinEtretinate
2011
The Multifunctional LigB Adhesin Binds Homeostatic Proteins with Potential Roles in Cutaneous Infection by Pathogenic Leptospira interrogans
Choy HA, Kelley MM, Croda J, Matsunaga J, Babbitt JT, Ko AI, Picardeau M, Haake DA. The Multifunctional LigB Adhesin Binds Homeostatic Proteins with Potential Roles in Cutaneous Infection by Pathogenic Leptospira interrogans. PLOS ONE 2011, 6: e16879. PMID: 21347378, PMCID: PMC3036719, DOI: 10.1371/journal.pone.0016879.Peer-Reviewed Original Research
1992
Ocular Manifestations of Pigmentary Disorders
Park S, Albert D, Bolognia J. Ocular Manifestations of Pigmentary Disorders. Dermatologic Clinics 1992, 10: 609-622. PMID: 1617818, DOI: 10.1016/s0733-8635(18)30328-0.ChaptersConceptsPigment epitheliumPigmentary disordersCutaneous pigmentary changesObserved neurologic abnormalitiesRetinal pigment epitheliumNevus of OtaDisorders of pigmentationHarada syndromeInflammatory causesVogt-KoyanagiOcular manifestationsUveal tractEye findingsOcular motilityNeurologic abnormalitiesNeurologic developmentFoveal hypoplasiaPigmentary changesMelanin-producing cellsPigmentary abnormalitiesIris heterochromiaMucous membranesVisual pathwayAcquired disordersFrequent association
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