Search results for "Alopecia Areata"

showing 10 items of 11 documents

Thyroid-associated orbitopathy is linked to gastrointestinal autoimmunity

2014

Summary Common autoimmune disorders tend to co-exist in the same subjects and cluster in families. The objective of this study was to determine the prevalence of autoimmune co-morbidity in patients with autoimmune thyroid disease (AITD) with and without thyroid-associated orbitopathy (TAO). This was a cross-sectional study conducted at an academic tertiary referral centre. Of 1310 patients with AITD [n = 777 or 59% with Graves' disease (GD) and n = 533, 41% with Hashimoto's thyroiditis (HT)] followed at a specialized joint thyroid–eye out-patient clinic, 176 (13·4%) had an adult type of the autoimmune polyglandular syndrome, 129 (9·8%) type 1 diabetes, 111 (8·5%) coeliac disease, 60 (4·6%) …

AdultMaleAdolescentAutoimmune GastritisImmunologyThyroid GlandAutoimmunityVitiligomedicine.disease_causeCoeliac diseaseThyroiditisAutoimmune DiseasesAutoimmunityYoung AdultOrbital DiseasesPrevalencemedicineHumansImmunology and AllergyChildAgedRetrospective StudiesAged 80 and overType 1 diabetesbusiness.industryOriginal ArticlesMiddle AgedAlopecia areatamedicine.diseaseThyroid DiseasesGastrointestinal TractGraves OphthalmopathyCross-Sectional StudiesChild PreschoolRheumatoid arthritisImmunologyFemalebusinessClinical and Experimental Immunology
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Local reactions to tick bites

2008

A retrospective histological and immunohistochemical study has been carried out in 25 cases of tick bites recorded in our Departments. The samples that included an attached tick showed a cement cone anchoring the mouthparts to the skin and a blood-soaked, spongiform appearance of the superficial dermis, with a mild neutrophilic and eosinophilic infiltration. The vessels displayed a loose multilayered endothelial proliferation, with plump endothelia, permeated with erythrocytes. A few of them were severed, allowing copious blood extravasation. The established lesions included the following: erythema chronicum migrans-like cases, foreign body granulomas-sometimes containing remnants of the mo…

AdultMalePathologymedicine.medical_specialtyHistologyErythemaAdolescentAlopecia AreataT-LymphocytesDermatologyBiologySettore MED/08 - Anatomia PatologicaSkin DiseasesLymphoid hyperplasiaPathology and Forensic MedicineHost-Parasite InteractionsLymphocytic InfiltrateDermisPseudolymphomamedicineSettore MED/35 - Malattie Cutanee E VenereeAnimalsHumansChildAgedRetrospective StudiesAged 80 and overB-LymphocytesIxodeslocal reactionInsect Bites and StingsHistologyGeneral MedicineAnatomyHyperplasiaMiddle Agedmedicine.diseaseHistology; local reactions; tick attacksArthropod mouthpartsExtravasationmedicine.anatomical_structuretick attacksErythema Chronicum MigransFemalemedicine.symptom
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Trichobiolight: A new, effective protocol in the treatment of androgenetic alopecia and telogen effluvium

2021

Androgenetic alopecia (AGA) with its precursor miniaturization of anagen phase (MA) and telogen effluvium (TE) represent nonscarring hair loss diseases which causes moderate to severe aesthetic and psychologic discomfort in affected people. Several therapeutic approaches have been tested through the latest decades, with different degree of success. In this study we aim to analyze the efficacy and outcome of an innovative therapeutic protocol, named TRICHOBIOLIGHT, a combination of active principles conveyed by mesotherapy directly on the scalp with a subsequent photobiostimulation session with LED light (630 nm). About 107 patients (49 women, 58 men, mean age 45-year-old) with clinical and …

MaleModerate to severemedicine.medical_specialtyAlopecia AreataDermatologyScarring alopeciaTelogen effluvium030207 dermatology & venereal diseases03 medical and health sciences0302 clinical medicinemedicineHumansAdverse effectScalpintegumentary systembusiness.industryAlopeciaGeneral MedicineMiddle Agedmedicine.diseaseDermatologyMesotherapyHair lossmedicine.anatomical_structureItaly030220 oncology & carcinogenesisScalpFemaleThickeningbusinessHairDermatologic Therapy
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Chronic active hepatitis associated with vitiligo, nail dystrophy, alopecia and a new variant of LKM antibodies

1990

In this report we describe the case of a 7-year-old boy, suffering from autoimmune-type chronic active hepatitis (AI-CAH) associated with vitiligo, nail dystrophy, alopecia areata and a variant of liver kidney microsomal (LKM) autoantibodies. This patient's antibodies are different from LKM-1 which are directed against cytochrome P450 db1. They react predominantly with perivenous hepatocytes in contrast to LKM-1 antibodies which homogeneously stain the whole liver lobule in immunofluorescence. In Western blot analysis this LKM variant reacts with a liver microsomal protein of approx. 50 kDa, but not with recombinant LKM-1 (cytochrome P450 db1) antigen. Immunosuppressive treatment led to a n…

MalePathologymedicine.medical_specialtyBlotting WesternVitiligoFluorescent Antibody TechniqueVitiligoImmunofluorescenceAutoimmune DiseasesNail DiseasesAntigenmedicineHumansChildskin and connective tissue diseasesAutoantibodiesHepatitis ChronicAutoimmune diseaseHepatitisintegumentary systemHepatologybiologymedicine.diagnostic_testbusiness.industryAutoantibodyGenetic VariationAlopeciaAlopecia areatamedicine.diseaseImmunologybiology.proteinAntibodybusinessJournal of Hepatology
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Pili Annulati Coincident with Alopecia Areata, Autoimmune Thyroid Disease, and Primary IgA Deficiency: Case Report and Considerations on the Literatu…

2012

Pili annulati is a rare autosomal dominant hair disorder clinically characterized by a pattern of alternating bright and dark bands of the hair, the bright bands appearing dark if observed by transmitted light. This pattern is due to the periodic occurrence of air-filled cavities along the hair cortex which scatter and reflect the light while precluding its transmission. A susceptibility region, including a possibly responsible Frizzled gene, has been mapped to the telomeric region of chromosome 12q, although a specific mutation has not been identified. The condition has sometimes been observed in concurrence with alopecia areata, and in this paper we report a case in whom the concomitant s…

Pathologymedicine.medical_specialtyAlopecia areataAutoimmune thyroid diseaseDermatologyPili annulati · Alopecia areata · Molecular changes · Autoimmune diseaseImmune systemAutoimmune diseaselcsh:DermatologymedicineSettore MED/35 - Malattie Cutanee E VenereeIgA deficiencyskin and connective tissue diseasesAutoimmune diseaseintegumentary systembusiness.industryPublished online: November 2012Molecular changeslcsh:RL1-803Alopecia areatamedicine.diseasePili annulatiHair rootHair DisorderImmunologysense organsbusinessPili annulatiCase Reports in Dermatology
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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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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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COVID‐19 and exacerbation of dermatological diseases: A review of the available literature

2021

Abstract Since the emergence of the new coronavirus disease 19 (COVID‐19) pandemic, there has been a concern for the patients with chronic autoimmune diseases including dermatological conditions over the potential exacerbation of these underlying conditions after infection with severe acute respiratory syndrome coronavirus‐2 (SARS‐CoV2). We performed a systematic review to evaluate presentations, postinfection change in the manifestation, diagnosis, and management of flare‐ups of underlying dermatologic disease in patients with COVID‐19. A total of 17 articles were recovered reporting on flare‐ups of dermatological disease including pemphigus vulgaris, psoriasis, subacute cutaneous lupus er…

medicine.medical_specialtyExacerbationShort ReportDiseaseSclerodermaSubacute cutaneous lupus erythematosusexacerbationShort ReportsCOVID‐19PsoriasismedicineHumansflare‐upworseningskin and connective tissue diseasesPandemicsSARS‐Cov2business.industrySARS-CoV-2Pemphigus vulgarispemphigusCOVID-19General MedicinepsoriasisAlopecia areatamedicine.diseaseDermatologydermatologyPemphigusRNA ViralbusinessDermatologic Therapy
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p53 Involvement in the control of murine hair follicle regression.

2001

p53 is a transcription factor mediating a variety of biological responses including apoptotic cell death. p53 was recently shown to control apoptosis in the hair follicle induced by ionizing radiation and chemotherapy, but its role in the apoptosis-driven physiological hair follicle regression (catagen) remains to be elucidated. Here, we show that p53 protein is strongly expressed and co-localized with apoptotic markers in the regressing hair follicle compartments during catagen. In contrast to wild-type mice, p53 knockout mice show significant retardation of catagen accompanied by significant decrease in the number of apoptotic cells in the hair matrix. Furthermore, p53 null hair follicles…

medicine.medical_specialtyTumor suppressor genemedicine.medical_treatmentDown-RegulationApoptosisBiologyPathology and Forensic MedicineTelogen effluviumMiceBcl-2-associated X proteinDownregulation and upregulationInternal medicineProto-Oncogene ProteinsmedicineAnimalsbcl-2-Associated X ProteinMice Knockoutintegumentary systemGrowth factorAlopecia areatamedicine.diseaseHair follicleCell biologyUp-RegulationMice Inbred C57BLEndocrinologymedicine.anatomical_structureInsulin-Like Growth Factor Binding Protein 3Proto-Oncogene Proteins c-bcl-2Knockout mousebiology.proteinCommentaryFemaleTumor Suppressor Protein p53Hair FollicleThe American journal of pathology
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Differentiation of frontal fibrosing alopecia and Lichen planopilaris on trichoscopy: A comprehensive review.

2021

Trichoscopy in dermatology has opened up the new concept in overcoming the optical challenge faced clinically. It reveals the diagnostic details to the depth of superficial dermis, and thereby increasing the clinician's diagnostic accuracy and the level of confidence. The importance of trichoscopy in cicatricial alopecia is very evident in the current scenario for its precise diagnosis. The clinical picture in delineating lichen planopilaris (LPP) and frontal fibrosing alopecia (FFA) from each other and also from other close mimickers such as androgenetic alopecia, alopecia areata, female patterned hair loss, and other cicatricial alopecia is bewildered due to its varied presentation and co…

medicine.medical_specialtyintegumentary systemAlopecia Areatabusiness.industryFrontal fibrosing alopecia610 MedizinLichen PlanusDiagnostic accuracyAlopeciaDermatologyAlopecia areatamedicine.diseaseLichen planopilarisDermatologyTrichoscopybody regionsstomatognathic diseasesCicatrixHair loss610 Medical sciencesmedicineHumansFemaleskin and connective tissue diseasesbusinessJournal of cosmetic dermatologyREFERENCES
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