Search results for "hair disease"

showing 7 items of 7 documents

Pilomatrixoma. Review of 205 cases.

2011

Podeu consultar la versió en castellà del document a: http://hdl.handle.net/2445/153543

AdultMalemedicine.medical_specialtySkin NeoplasmsAdolescentJawsEpitheliumLesionYoung AdultMedicineHumansYoung adultChildGeneral DentistryTumorsAgedRetrospective StudiesMaxil·larsbusiness.industryIncidence (epidemiology)InfantRetrospective cohort studyMiddle Aged:CIENCIAS MÉDICAS [UNESCO]PilomatrixomaDermatologySurgeryOtorhinolaryngologyChild PreschoolUNESCO::CIENCIAS MÉDICASPilomatrixomaSurgeryFemaleMaxillary Sinus NeoplasmDifferential diagnosisPresentation (obstetrics)medicine.symptombusinessHair DiseasesEpiteliMedicina oral, patologia oral y cirugia bucal
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Impaired GH secretion in patients with SHOX deficiency and efficacy of recombinant human GH therapy.

2012

<b><i>Background/Aims:</i></b> Mutations of the short stature homeobox-containing <i>(SHOX)</i> gene on the pseudoautosomal region of the sex chromosomes cause short stature. GH treatment has been recently proposed to improve height in short patients with SHOX deficiency. The aim of this study was to evaluate GH secretion and analyze growth and safety of recombinant human GH (rhGH) therapy in short children and adolescents with SHOX deficiency. <b><i>Patients and Design:</i></b> We studied 16 patients (10 females; 9.7 ± 2.9 years old; height –2.46 ± 0.82 standard deviation score, SDS) with SHOX deficiency. All subjects underwent au…

MaleLanger-Giedion SyndromeEndocrinology Diabetes and MetabolismSHOX deficiencyPseudoautosomal regionMadelung deformityLer Weill syndromelaw.inventionEndocrinologySettore MED/38 - Pediatria Generale E SpecialisticaShort Stature Homeobox ProteinGH treatmentShort Stature Homeobox ProteinlawSHOX DeficiencyChildGrowth DisordersHuman Growth HormoneGrowth hormone secretionRecombinant ProteinsGHRecombinant Human GHChild PreschoolRecombinant DNAFemalemedicine.symptomSHOX Deficiencymedicine.medical_specialtyAdolescentNoseOsteochondrodysplasiasShort statureFingersInternal medicinemedicineHumansLéri–Weill dyschondrosteosisGeneLeri-Weill dyschondrosteosiHomeodomain Proteinsbusiness.industrymedicine.diseaseBody HeightSHOX Deficiency; Ler Weill syndrome; Recombinant Human GHShort statureEndocrinologyGrowth HormonePediatrics Perinatology and Child HealthbusinessHair DiseasesSHOX
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Matrical carcinoma with prominent melanocytic hyperplasia (malignant melanocytic matricoma?) A report of two cases.

2003

Melanocytic matricoma is a recently described lesion characterized by well-circumscribed nodules composed of matrical and supramatrical cells with clustered ghost cells, and admixed pigmented dendritic melanocytes, with no cyst formation or connection to the epidermis or pre-existing hair follicles. Although variable cytologic atypia and frequent mitoses in the epithelial component may be present, given the well-defined margins and absence of tumor recurrences, these lesions were initially considered benign neoplasms, and not matrical carcinoma. Theoretically, the detection of numerous melanocytes in matrical carcinoma should not be surprising, but is in fact a very unusual feature. A case …

Malemedicine.medical_specialtyPathologySkin NeoplasmsDermatologyBiologyPathology and Forensic MedicineLesionMatrical CarcinomamedicineCarcinomaHumansAgedAnatomical pathologyGhost cellGeneral MedicineMiddle Agedmedicine.diseasePilomatrixomaImmunohistochemistrymedicine.anatomical_structureImmunohistochemistryMelanocytesHistopathologyEpidermismedicine.symptomHair DiseasesThe American Journal of dermatopathology
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Nodular Lesion in Cheek With a Hair Tuft

2017

Trichostasis spinulosa is a rarely diagnosed disorder of the pilosebaceous unit, characterized by retention of telogen hairs within the dilated follicles. A hair tuft can be seen protruding from the follicles. We present a case of trichostasis spinulosa associated with intradermal melanocytic nevi, where dermoscopy helps to identify this entity.

Skin NeoplasmsKeratosisDermoscopyDermatologyConservative TreatmentPathology and Forensic MedicineDiagnosis Differential030207 dermatology & venereal diseases03 medical and health sciences0302 clinical medicineTrichostasis spinulosaHumansMedicineNevusTuftAgedNevus Pigmentedintegumentary systembusiness.industryPruritusBiopsy NeedleKeratosisAnatomyGeneral MedicineCheekmedicine.diseaseHair follicleImmunohistochemistryCheekmedicine.anatomical_structureHair disease030220 oncology & carcinogenesisFemaleDifferential diagnosisHair DiseasesbusinessHair FollicleFollow-Up StudiesThe American Journal of Dermatopathology
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Trichostasis spinulosa misdiagnosed as alopecia areata.

2020

medicine.medical_specialtyAlopecia Areatabusiness.industryPruritusDermatologyGeneral MedicineKeratosisAlopecia areatamedicine.diseaseDermatologymedicineTrichostasis spinulosaHumansDiagnostic ErrorsbusinessHair DiseasesDermatologic therapyREFERENCES
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Clinical, Microscopic and Ultrastructural Findings in a Case of Short Anagen Syndrome

2017

Short anagen syndrome is an uncommon and recently described disease characterized by many telogen hairs and short maximum hair length. We report here the case of a 3-year-old girl whose short, sparse, fine hair since birth was consistent with short anagen syndrome. X-ray microanalysis demonstrated normal composition of the main bioelements of her hairs.

medicine.medical_specialtyDermatology030207 dermatology & venereal diseases03 medical and health sciences0302 clinical medicineotorhinolaryngologic diseasesmedicineHumansElectron probe microanalysisintegumentary systembusiness.industrySyndromemedicine.diseaseShort anagen syndromeDermatologybody regionsChild Preschool030220 oncology & carcinogenesisPediatrics Perinatology and Child HealthUltrastructureFemalesense organsHair DiseasesbusinessElectron Probe MicroanalysisHairPediatric Dermatology
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Pili Torti: A Feature of Numerous Congenital and Acquired Conditions

2021

Pili torti is a rare condition characterized by the presence of the hair shaft, which is flattened at irregular intervals and twisted 180° along its long axis. It is a form of hair shaft disorder with increased fragility. The condition is classified into inherited and acquired. Inherited forms may be either isolated or associated with numerous genetic diseases or syndromes (e.g., Menkes disease, Björnstad syndrome, Netherton syndrome, and Bazex-Dupré-Christol syndrome). Moreover, pili torti may be a feature of various ectodermal dysplasias (such as Rapp-Hodgkin syndrome and Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome). Acquired pili torti was described in numerous forms of …

medicine.medical_specialtyDiscoid lupus erythematosushair shaft disorderhair diseaseReviewmedicineNetherton syndromehair shaft abnormalitiesPili tortiintegumentary systembusiness.industrypili tortitrichoscopyRBjörnstad syndromeGeneral MedicineAlopecia areatamedicine.diseaseDermatologyTrichoscopyHair diseasetwisted hairMedicinemedicine.symptombusinessFolliculitis decalvansJournal of Clinical Medicine
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