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  1 / 4458 MEDLINE  
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[PMID]:22727533
[Au] Autor:Besemer F; Verschoor AJ; Diamant M; Hoogma RP
[Ad] Dirección:Department of Internal Medicine, Groene Hart Hospital, Bleulandweg 10, 2800 BB Gouda Netherlands. fbesemer@gmail.com
[Ti] Título:Vesiculopustular dermatosis: an uncommon side-effect of liraglutide?
[So] Fuente:J Diabetes Complications;26(5):458-9, 2012 Sep-Oct.
[Is] ISSN:1873-460X
[Cp] País de publicación:United States
[La] Idioma:eng
[Ab] Resumen:Liraglutide is a GLP-1 receptor agonist, a novel medication for type 2 diabetes. We describe a case of pustules in a patient recently started on liraglutide. Common side effects of liraglutide are gastrointestinal disorders. Skin and tissue reactions are less well-known side effects. Liraglutide could be the cause of skin eruptions in this patient, possibly by immunogenicity.
[Mh] Términos MeSH primario: Diabetes Mellitus Tipo 2/complicaciones
Erupciones por Medicamentos/diagnóstico
Péptido 1 Similar al Glucagón/análogos & derivados
Hipoglucemiantes/efectos adversos
Enfermedades Cutáneas Vesiculoampollosas/diagnóstico
[Mh] Términos MeSH secundario: Diabetes Mellitus Tipo 2/quimioterapia
Diagnóstico Diferencial
Monitoreo de Drogas
Eructación/etiología
Fiebre/etiología
Péptido 1 Similar al Glucagón/efectos adversos
Péptido 1 Similar al Glucagón/uso terapéutico
Humanos
Hipoglucemiantes/uso terapéutico
Masculino
Mediana Edad
Enfermedades Cutáneas Vesiculoampollosas/inducido químicamente
Enfermedades Cutáneas Vesiculoampollosas/etiología
Tórax
[Pt] Tipo de publicación:CASE REPORTS; JOURNAL ARTICLE
[Nm] Nombre de substancia:
0 (Hypoglycemic Agents); 839I73S42A (liraglutide); 89750-14-1 (Glucagon-Like Peptide 1)
[Em] Mes de ingreso:1301
[Cu] Fecha actualización por clase:130513
[Lr] Fecha última revisión:130513
[Sb] Subgrupo de revista:IM
[Da] Fecha de ingreso para procesamiento:120907
[St] Status:MEDLINE
[do] DOI:10.1016/j.jdiacomp.2012.05.018


  2 / 4458 MEDLINE  
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[PMID]:23151326
[Au] Autor:Zweegers J; Bovenschen HJ
[Ad] Dirección:Máxima Medisch Centrum, afd. Dermatologie, Veldhoven, the Netherlands.
[Ti] Título:[A woman with skin abnormalities around the mouth].
[Ti] Título:Een vrouw met huidafwijkingen rond de mond..
[So] Fuente:Ned Tijdschr Geneeskd;156(46):A4613, 2012.
[Is] ISSN:1876-8784
[Cp] País de publicación:Netherlands
[La] Idioma:dut
[Ab] Resumen:A 33-year-old healthy woman consulted her dermatologist when an acute and painful perioral pustular dermatosis erupted one day after she had taken azitromycin for a throat infection. A preliminary diagnosis of acute localized exanthematous pustulosis (ALEP) was made, which was later confirmed by cultures and histopathological examination. Medication was cessated immediately and the dermatosis disappeared completely afterwards.
[Mh] Términos MeSH primario: Antibacterianos/efectos adversos
Azitromicina/efectos adversos
Exantema/inducido químicamente
Enfermedades Cutáneas Vesiculoampollosas/inducido químicamente
[Mh] Términos MeSH secundario: Adulto
Antibacterianos/uso terapéutico
Azitromicina/uso terapéutico
Exantema/diagnóstico
Femenino
Humanos
Enfermedades Cutáneas Vesiculoampollosas/diagnóstico
[Pt] Tipo de publicación:CASE REPORTS; ENGLISH ABSTRACT; JOURNAL ARTICLE
[Nm] Nombre de substancia:
0 (Anti-Bacterial Agents); 83905-01-5 (Azithromycin)
[Em] Mes de ingreso:1305
[Sb] Subgrupo de revista:IM
[Da] Fecha de ingreso para procesamiento:121115
[St] Status:MEDLINE


  3 / 4458 MEDLINE  
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[PMID]:22940757
[Au] Autor:Matsumura Y; Miyachi Y
[Ad] Dirección:Department of Dermatology, Kyoto University School of Medicine, 54 Shogoin-Kawahara-cho, Sakyo-ku, Kyoto 606-8507, Japan. yumatsu@kuhp.kyoto-u.ac.jp
[Ti] Título:Atypical clinical appearance of eosinophilic pustular folliculitis of seborrheic areas of the face.
[So] Fuente:Eur J Dermatol;22(5):658-62, 2012 Sep-Oct.
[Is] ISSN:1952-4013
[Cp] País de publicación:France
[La] Idioma:eng
[Ab] Resumen:Eosinophilic pustular folliculitis is a pruritic eruption that preferentially involves the face. It is characterized by well-demarcated erythema, extending peripherally with a central clearing and pigmentation, together with sterile pustules lining the periphery. We describe five cases of eosinophilic pustular folliculitis with pruritic papules and erythema on seborrheic areas of the face, which lacked the typical features of classic eosinophilic pustular folliculitis--pustules and peripheral extension--but showed eosinophilic infiltration of the hair follicles, histologically. The eruption quickly responded to oral indomethacin except for one case that responded to tranilast and one case that was associated with acquired immunodeficiency syndrome, with recurrences in defined areas of the face. Our findings in these cases suggest that eosinophilic pustular folliculitis may vary in clinical appearance.
[Mh] Términos MeSH primario: Eosinofilia/patología
Dermatosis Facial/patología
Foliculitis/patología
Enfermedades Cutáneas Vesiculoampollosas/patología
[Mh] Términos MeSH secundario: Adulto
Antiinflamatorios no Esteroideos/uso terapéutico
Diagnóstico Diferencial
Eosinofilia/quimioterapia
Dermatosis Facial/quimioterapia
Femenino
Foliculitis/quimioterapia
Humanos
Inmunosupresores/uso terapéutico
Indometacina/uso terapéutico
Masculino
Mediana Edad
Recurrencia
Enfermedades Cutáneas Vesiculoampollosas/quimioterapia
Tacrolimus/uso terapéutico
ortoaminobenzoatos/uso terapéutico
[Pt] Tipo de publicación:CASE REPORTS; JOURNAL ARTICLE
[Nm] Nombre de substancia:
0 (Anti-Inflammatory Agents, Non-Steroidal); 0 (Immunosuppressive Agents); 0 (ortho-Aminobenzoates); 109581-93-3 (Tacrolimus); 53-86-1 (Indomethacin); 53902-12-8 (tranilast)
[Em] Mes de ingreso:1305
[Sb] Subgrupo de revista:IM
[Da] Fecha de ingreso para procesamiento:121024
[St] Status:MEDLINE
[do] DOI:10.1684/ejd.2012.1825


  4 / 4458 MEDLINE  
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[PMID]:22913880
[Au] Autor:Dietrich N; Beltraminelli H; Borradori L
[Ti] Título:Linear IgA bullous dermatosis mimicking a neutrophilic dermatosis.
[So] Fuente:Eur J Dermatol;22(5):713-4, 2012 Sep-Oct.
[Is] ISSN:1952-4013
[Cp] País de publicación:France
[La] Idioma:eng
[Mh] Términos MeSH primario: Dermatosis Bullosa IgA Lineal/diagnóstico
[Mh] Términos MeSH secundario: Anciano de 80 o más Años
Antiinflamatorios no Esteroideos/efectos adversos
Diagnóstico Diferencial
Diclofenaco/efectos adversos
Erupciones por Medicamentos/diagnóstico
Erupciones por Medicamentos/patología
Femenino
Humanos
Inmunoglobulina A/metabolismo
Dermatosis Bullosa IgA Lineal/inducido químicamente
Dermatosis Bullosa IgA Lineal/quimioterapia
Enfermedades Cutáneas Vesiculoampollosas/diagnóstico
[Pt] Tipo de publicación:CASE REPORTS; LETTER
[Nm] Nombre de substancia:
0 (Anti-Inflammatory Agents, Non-Steroidal); 0 (Immunoglobulin A); 15307-86-5 (Diclofenac)
[Em] Mes de ingreso:1305
[Sb] Subgrupo de revista:IM
[Da] Fecha de ingreso para procesamiento:121024
[St] Status:MEDLINE
[do] DOI:10.1684/ejd.2012.1809


  5 / 4458 MEDLINE  
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[PMID]:22681514
[Au] Autor:Walsh S; Creamer D
[Ti] Título:A diagnostic challenge: acute generalized exanthematous pustulosis or pustular psoriasis due to terbinafine: comment.
[So] Fuente:Clin Exp Dermatol;37(8):919, 2012 Dec.
[Is] ISSN:1365-2230
[Cp] País de publicación:England
[La] Idioma:eng
[Mh] Términos MeSH primario: Pustulosis Exantemática Aguda Generalizada/diagnóstico
Erupciones por Medicamentos/diagnóstico
Psoriasis/diagnóstico
Enfermedades Cutáneas Vesiculoampollosas/diagnóstico
[Mh] Términos MeSH secundario: Humanos
Masculino
[Pt] Tipo de publicación:COMMENT; LETTER
[Em] Mes de ingreso:1305
[Sb] Subgrupo de revista:IM
[Da] Fecha de ingreso para procesamiento:121122
[St] Status:MEDLINE
[do] DOI:10.1111/j.1365-2230.2012.04407.x


  6 / 4458 MEDLINE  
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[PMID]:22548627
[Au] Autor:Malik M; Perkins W; Leach I
[Ad] Dirección:Department of Dermatology, Queens Medical Centre, Nottingham University Hospital, Nottingham, UK. moona.malik@nuh.nhs.uk
[Ti] Título:Anti-neutrophil cytoplasmic antibody-positive neutrophilic dermatosis of the dorsal hands.
[So] Fuente:Clin Exp Dermatol;37(8):869-70, 2012 Dec.
[Is] ISSN:1365-2230
[Cp] País de publicación:England
[La] Idioma:eng
[Ab] Resumen:Neutrophilic dermatosis of the hands is a localized variant of Sweet syndrome (SS). It was first reported in 1995, and is an uncommon condition, with < 100 cases reported to date. The female preponderance, morphological and histological features, and response to treatment are similar to SS, but it differs in its distribution on the body. There may also be a lack of systemic features and inconsistent laboratory findings. Significantly, about half of all cases are associated with haematological problems, i.e. myelodysplasia and leukaemia. Other cases may be associated with ulcerative colitis or solid tumours. We describe a case of a 71-year-old man with neutrophilic dermatoses of the hands, who also had involvement of the lips. There was an associated rise in his anti-neutrophil cytoplasmic antibody level, which corresponded with the activity of the disease.
[Mh] Términos MeSH primario: Anticuerpos Citoplasmáticos Antineutrófilo/metabolismo
Dermatosis de la Mano/inmunología
Enfermedades de los Labios/inmunología
Enfermedades Cutáneas Vesiculoampollosas/inmunología
[Mh] Términos MeSH secundario: Anciano
Dermatosis de la Mano/patología
Humanos
Enfermedades de los Labios/patología
Masculino
Enfermedades Cutáneas Vesiculoampollosas/patología
[Pt] Tipo de publicación:CASE REPORTS; JOURNAL ARTICLE
[Nm] Nombre de substancia:
0 (Antibodies, Antineutrophil Cytoplasmic)
[Em] Mes de ingreso:1305
[Sb] Subgrupo de revista:IM
[Da] Fecha de ingreso para procesamiento:121122
[St] Status:MEDLINE
[do] DOI:10.1111/j.1365-2230.2012.04359.x


  7 / 4458 MEDLINE  
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[PMID]:22563626
[Au] Autor:Patel NP; Laguda B; Roberts NM; Francis ND; Agnew K
[Ti] Título:Treatment of eosinophilic pustulosis of infancy with topical tacrolimus.
[So] Fuente:Br J Dermatol;167(5):1189-91, 2012 Nov.
[Is] ISSN:1365-2133
[Cp] País de publicación:England
[La] Idioma:eng
[Mh] Términos MeSH primario: Eosinofilia/quimioterapia
Foliculitis/quimioterapia
Inmunosupresores/administración & dosificación
Enfermedades Cutáneas Vesiculoampollosas/quimioterapia
Tacrolimus/administración & dosificación
[Mh] Términos MeSH secundario: Administración Tópica
Eosinofilia/patología
Foliculitis/patología
Humanos
Lactante
Masculino
Enfermedades Cutáneas Vesiculoampollosas/patología
Resultado del Tratamiento
[Pt] Tipo de publicación:CASE REPORTS; LETTER
[Nm] Nombre de substancia:
0 (Immunosuppressive Agents); 109581-93-3 (Tacrolimus)
[Em] Mes de ingreso:1304
[Sb] Subgrupo de revista:IM
[Da] Fecha de ingreso para procesamiento:121030
[St] Status:MEDLINE
[do] DOI:10.1111/j.1365-2133.2012.11045.x


  8 / 4458 MEDLINE  
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[PMID]:22876746
[Au] Autor:van Beek N; Rentzsch K; Probst C; Komorowski L; Kasperkiewicz M; Fechner K; Bloecker IM; Zillikens D; Stöcker W; Schmidt E
[Ad] Dirección:Department of Dermatology, University of Luebeck, Luebeck, Germany.
[Ti] Título:Serological diagnosis of autoimmune bullous skin diseases: prospective comparison of the BIOCHIP mosaic-based indirect immunofluorescence technique with the conventional multi-step single test strategy.
[So] Fuente:Orphanet J Rare Dis;7:49, 2012.
[Is] ISSN:1750-1172
[Cp] País de publicación:England
[La] Idioma:eng
[Ab] Resumen:BACKGROUND: Various antigen-specific immunoassays are available for the serological diagnosis of autoimmune bullous diseases. However, a spectrum of different tissue-based and monovalent antigen-specific assays is required to establish the diagnosis. BIOCHIP mosaics consisting of different antigen substrates allow polyvalent immunofluorescence (IF) tests and provide antibody profiles in a single incubation. METHODS: Slides for indirect IF were prepared, containing BIOCHIPS with the following test substrates in each reaction field: monkey esophagus, primate salt-split skin, antigen dots of tetrameric BP180-NC16A as well as desmoglein 1-, desmoglein 3-, and BP230gC-expressing human HEK293 cells. This BIOCHIP mosaic was probed using a large panel of sera from patients with pemphigus vulgaris (PV, n=65), pemphigus foliaceus (PF, n=50), bullous pemphigoid (BP, n=42), and non-inflammatory skin diseases (n=97) as well as from healthy blood donors (n=100). Furthermore, to evaluate the usability in routine diagnostics, 454 consecutive sera from patients with suspected immunobullous disorders were prospectively analyzed in parallel using a) the IF BIOCHIP mosaic and b) a panel of single antibody assays as commonly used by specialized centers. RESULTS: Using the BIOCHIP mosaic, sensitivities of the desmoglein 1-, desmoglein 3-, and NC16A-specific substrates were 90%, 98.5% and 100%, respectively. BP230 was recognized by 54% of the BP sera. Specificities ranged from 98.2% to 100% for all substrates. In the prospective study, a high agreement was found between the results obtained by the BIOCHIP mosaic and the single test panel for the diagnosis of BP, PV, PF, and sera without serum autoantibodies (Cohen's κ between 0.88 and 0.97). CONCLUSIONS: The BIOCHIP mosaic contains sensitive and specific substrates for the indirect IF diagnosis of BP, PF, and PV. Its diagnostic accuracy is comparable with the conventional multi-step approach. The highly standardized and practical BIOCHIP mosaic will facilitate the serological diagnosis of autoimmune blistering diseases.
[Mh] Términos MeSH primario: Enfermedades Autoinmunes/diagnóstico
Técnica del Anticuerpo Fluorescente Indirecta/métodos
Enfermedades Cutáneas Vesiculoampollosas/diagnóstico
[Mh] Términos MeSH secundario: Secuencia de Bases
Cartilla de ADN
Células HEK293
Humanos
Estudios Prospectivos
[Pt] Tipo de publicación:COMPARATIVE STUDY; JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T; VALIDATION STUDIES
[Nm] Nombre de substancia:
0 (DNA Primers)
[Em] Mes de ingreso:1304
[Sb] Subgrupo de revista:IM
[Da] Fecha de ingreso para procesamiento:130101
[St] Status:MEDLINE
[do] DOI:10.1186/1750-1172-7-49


  9 / 4458 MEDLINE  
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[PMID]:23021058
[Au] Autor:Magro CM; Roberts-Barnes J; Crowson AN
[Ad] Dirección:Department of Pathology and Laboratory Medicine, Weill Medical College of Cornell University, New York, NY 10065, USA.
[Ti] Título:Direct immunofluorescence testing in the diagnosis of immunobullous disease, collagen vascular disease, and vascular injury syndromes.
[So] Fuente:Dermatol Clin;30(4):763-98, viii, 2012 Oct.
[Is] ISSN:1558-0520
[Cp] País de publicación:United States
[La] Idioma:eng
[Ab] Resumen:Direct and indirect immunofluorescence (IF) plays a role in the evaluation of immunobullous diseases and their mimics, and in the investigation of vascular injury syndromes and autoimmune connective tissue disease (CTD). IF mapping may be an important adjunct in the assessment of congenital epidermolysis bullosa syndromes and in Alport disease, in which antibodies are directed at certain components of the basement membrane zone to assay for their deficiency. In many cases of immunobullous and autoimmune CTDs, correlation with direct IF results is useful and often decisive in lesional evaluation and thus in patient management.
[Mh] Términos MeSH primario: Enfermedades Autoinmunes/diagnóstico
Enfermedades del Tejido Conjuntivo/diagnóstico
Inmunoglobulina A/inmunología
Enfermedades Cutáneas Vesiculoampollosas/diagnóstico
Vasculitis/inmunología
[Mh] Términos MeSH secundario: Anticuerpos Citoplasmáticos Antineutrófilo/metabolismo
Síndrome Antifosfolípido/diagnóstico
Síndrome Antifosfolípido/inmunología
Autoanticuerpos/sangre
Autoantígenos/metabolismo
Enfermedades Autoinmunes/inmunología
Enfermedades Autoinmunes/patología
Membrana Basal/metabolismo
Colágeno/metabolismo
Enfermedades del Tejido Conjuntivo/inmunología
Enfermedades del Tejido Conjuntivo/patología
Técnica del Anticuerpo Fluorescente Directa
Técnica del Anticuerpo Fluorescente Indirecta
Humanos
Lupus Eritematoso Sistémico/diagnóstico
Lupus Eritematoso Sistémico/inmunología
Lupus Eritematoso Sistémico/patología
Microscopía Electrónica
Nefritis Hereditaria/diagnóstico
Enfermedades Cutáneas Vesiculoampollosas/inmunología
Enfermedades Cutáneas Vesiculoampollosas/patología
Vasculitis/diagnóstico
Vasculitis/metabolismo
[Pt] Tipo de publicación:JOURNAL ARTICLE; REVIEW
[Nm] Nombre de substancia:
0 (Antibodies, Antineutrophil Cytoplasmic); 0 (Autoantibodies); 0 (Autoantigens); 0 (Immunoglobulin A); 9007-34-5 (Collagen)
[Em] Mes de ingreso:1304
[Sb] Subgrupo de revista:IM
[Da] Fecha de ingreso para procesamiento:121001
[St] Status:MEDLINE


  10 / 4458 MEDLINE  
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[PMID]:23021053
[Au] Autor:Fung MA; Barr KL
[Ad] Dirección:UC Davis Dermatopathology Service, Department of Dermatology, University of California Davis School of Medicine, 3301 C Street, Suite 1400, Sacramento, CA 95816, USA. maxwell.fung@ucdmc.ucdavis.edu
[Ti] Título:Current knowledge in inflammatory dermatopathology.
[So] Fuente:Dermatol Clin;30(4):667-84, vii, 2012 Oct.
[Is] ISSN:1558-0520
[Cp] País de publicación:United States
[La] Idioma:eng
[Ab] Resumen:The complex and fascinating spectrum of inflammatory skin disease, and the comprehension of it, is ever expanding and evolving. During the first decade of the 21st century, numerous advances in the understanding of inflammatory disease mechanisms have occurred, particularly in psoriasis and atopic dermatitis. Continuation of this trend will assure a future in which molecular tests for biomarkers of immediate clinical relevance are used in routine patient care, not only for diagnosis but also for prognosis and management. This article focuses on selected recent or noteworthy developments that are clinically relevant for the histologic diagnosis of inflammatory skin diseases.
[Mh] Términos MeSH primario: Dermatitis/patología
Glucagonoma/diagnóstico
Micosis Fungoide/diagnóstico
Eritema Necrolítico Migratorio/diagnóstico
Neoplasias Pancreáticas/diagnóstico
Neoplasias Cutáneas/diagnóstico
[Mh] Términos MeSH secundario: Arteritis/patología
Dermatitis/diagnóstico
Diagnóstico Diferencial
Erupciones por Medicamentos/patología
Humanos
Levamisol/efectos adversos
Lupus Eritematoso Cutáneo/patología
Eritema Necrolítico Migratorio/patología
Síndromes Paraneoplásicos/patología
Trastornos por Fotosensibilidad/patología
Pitiriasis Rubra Pilaris/patología
Enfermedades Cutáneas Genéticas/patología
Enfermedades Cutáneas Vesiculoampollosas/patología
Neoplasias Cutáneas/patología
Síndrome de Sweet/patología
[Pt] Tipo de publicación:JOURNAL ARTICLE; REVIEW
[Nm] Nombre de substancia:
14769-73-4 (Levamisole)
[Em] Mes de ingreso:1304
[Sb] Subgrupo de revista:IM
[Da] Fecha de ingreso para procesamiento:121001
[St] Status:MEDLINE



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