Base de dados : MEDLINE
Pesquisa : C17.800.862 [Categoria DeCS]
Referências encontradas : 1406 [refinar]
Mostrando: 1 .. 10   no formato [Detalhado]

página 1 de 141 ir para página                         

  1 / 1406 MEDLINE  
              next record last record
seleciona
para imprimir
Fotocópia
Texto completo
[PMID]:28822558
[Au] Autor:Peterman CM; Vadeboncoeur S; Mulliken JB; Fishman SJ; Liang MG
[Ad] Endereço:Tufts University School of Medicine, Boston, Massachusetts; Department of Dermatology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts; Vascular Anomalies Center, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts.
[Ti] Título:Wilms tumor screening in diffuse capillary malformation with overgrowth and macrocephaly-capillary malformation: A retrospective study.
[So] Source:J Am Acad Dermatol;77(5):874-878, 2017 Nov.
[Is] ISSN:1097-6787
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:BACKGROUND: CLOVES (congenital lipomatous overgrowth, vascular malformations, epidermal nevi, and skeletal anomalies) syndrome is associated with regional bony and/or soft tissue overgrowth, capillary malformation, and an increased risk for Wilms tumor. OBJECTIVE: To evaluate the frequency of Wilms tumor in patients with 2 similar conditions: diffuse capillary malformation with overgrowth (DCMO) and macrocephaly-capillary malformation (M-CM). METHODS: Culling our Vascular Anomalies Center database, we retrospectively reviewed patients in whom DCMO and M-CM had been diagnosed and who were evaluated between 1998 and 2016 for possible development of Wilms tumor. Patients younger than 8 years of age at their last visit and not seen in more than 2 years were contacted for follow-up. RESULTS: The study comprised 89 patients: 67 with DCMO, 17 with M-CM, and 5 with an indeterminate diagnosis. No case of Wilms tumor was found in these groups. LIMITATIONS: Some patients were younger than 8 years of age at last follow-up visit and the sample size was small. CONCLUSION: Patients with DCMO do not appear to be at increased risk for Wilms tumor. Screening is probably unnecessary in DCMO unless there is associated hemihypertrophy. Although there were no cases in our cohort, there are 2 reports of M-CM associated with Wilms tumor in the literature.
[Mh] Termos MeSH primário: Anormalidades Múltiplas/epidemiologia
Capilares/anormalidades
Neoplasias Renais/epidemiologia
Megalencefalia/epidemiologia
Dermatopatias Vasculares/epidemiologia
Telangiectasia/congênito
Malformações Vasculares/epidemiologia
Tumor de Wilms/epidemiologia
[Mh] Termos MeSH secundário: Anormalidades Múltiplas/diagnóstico por imagem
Anormalidades Múltiplas/patologia
Distribuição por Idade
Capilares/diagnóstico por imagem
Capilares/patologia
Pré-Escolar
Estudos de Coortes
Comorbidade
Bases de Dados Factuais
Feminino
Seguimentos
Seres Humanos
Incidência
Lactente
Recém-Nascido
Neoplasias Renais/diagnóstico por imagem
Neoplasias Renais/patologia
Lipoma/diagnóstico por imagem
Lipoma/epidemiologia
Lipoma/patologia
Imagem por Ressonância Magnética
Masculino
Megalencefalia/diagnóstico por imagem
Megalencefalia/patologia
Anormalidades Musculoesqueléticas/diagnóstico por imagem
Anormalidades Musculoesqueléticas/epidemiologia
Anormalidades Musculoesqueléticas/patologia
Triagem Neonatal
Nevo/diagnóstico por imagem
Nevo/epidemiologia
Nevo/patologia
Doenças Raras
Estudos Retrospectivos
Medição de Risco
Índice de Gravidade de Doença
Distribuição por Sexo
Dermatopatias Vasculares/diagnóstico por imagem
Dermatopatias Vasculares/patologia
Telangiectasia/diagnóstico por imagem
Telangiectasia/epidemiologia
Telangiectasia/patologia
Fatores de Tempo
Malformações Vasculares/diagnóstico por imagem
Malformações Vasculares/patologia
Tumor de Wilms/diagnóstico por imagem
Tumor de Wilms/patologia
[Pt] Tipo de publicação:COMPARATIVE STUDY; JOURNAL ARTICLE
[Em] Mês de entrada:1711
[Cu] Atualização por classe:171102
[Lr] Data última revisão:
171102
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170821
[St] Status:MEDLINE


  2 / 1406 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo
[PMID]:28442217
[Au] Autor:Gru AA; Salavaggione AL
[Ad] Endereço:Department of Pathology & Dermatology, University of Virginia, United States. Electronic address: AAG4B@hscmail.mcc.virginia.edu.
[Ti] Título:Vasculopathic and vasculitic dermatoses.
[So] Source:Semin Diagn Pathol;34(3):285-300, 2017 May.
[Is] ISSN:0740-2570
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:The inflammatory and non-inflammatory disorders affecting the blood vessels are an important cause of death among patients. Additionally, some of the findings could be very subtle, while the consequences of misdiagnosis tragic. There is a limited number of factors by which the cutaneous blood vessels can be affected and the most common examples in the clinical practice will be discussed here: non-inflammatory purpuras; vascular-occlusive disorders; urticarias; vasculitides; and neutrophilic dermatoses.
[Mh] Termos MeSH primário: Dermatopatias Vasculares/patologia
[Mh] Termos MeSH secundário: Seres Humanos
[Pt] Tipo de publicação:JOURNAL ARTICLE; REVIEW
[Em] Mês de entrada:1707
[Cu] Atualização por classe:170726
[Lr] Data última revisão:
170726
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170427
[St] Status:MEDLINE


  3 / 1406 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo
[PMID]:28363337
[Au] Autor:Henneton P; Frank M; Litvinova E; Miranda S; Messas E; Darnige L
[Ad] Endereço:Centre de référence des maladies vasculaires rares, hôpital européen Georges-Pompidou, AP-HP, 75908 Paris cedex 15, France; Médecine interne et médecine vasculaire, hôpital Saint-Éloi, CHRU de Montpellier, 34295 Montpellier cedex 5, France.
[Ti] Título:[Gardner-Diamond syndrome in a young man: A case report and literature review].
[Ti] Título:Syndrome de Gardner-Diamond : à propos d'un cas chez un homme jeune et revue de la littérature..
[So] Source:Rev Med Interne;38(9):623-627, 2017 Sep.
[Is] ISSN:1768-3122
[Cp] País de publicação:France
[La] Idioma:fre
[Ab] Resumo:INTRODUCTION: Gardner-Diamond syndrome is a rare condition secondary to a sensitization to self-erythrocytes. It is predominantly seen in women and presents as a painful ecchymotic disorder. An underlying psychiatric disease or a triggering psychological stress is of important diagnostic value. CASE REPORT: We report a 24-year-old patient who presented with intermittent spontaneous painful ecchymosis since 5 years. Complementary investigations failed to identify an organic disorder. Gardner-Diamond syndrome was retained because of the clinical presentation, the negativity of diagnostic work-up and the identification of a psychological trauma. Patient management (pain, psychological support) is difficult, justifying a multidisciplinary approach. CONCLUSION: Gardner-Diamond syndrome is a rare and unrecognized disorder, which should be discussed in the presence of ecchymotic or purpuric lesions that do not have a diagnostic orientation. Early recognition of this disorder enables initiation of an appropriate management, but also limits unnecessary additional explorations.
[Mh] Termos MeSH primário: Doenças Autoimunes/diagnóstico
Transtornos Autoinduzidos/diagnóstico
Transtornos Psicóticos/diagnóstico
Dermatopatias Vasculares/diagnóstico
[Mh] Termos MeSH secundário: Doenças Autoimunes/genética
Doenças Autoimunes/patologia
Diagnóstico Diferencial
Transtornos Autoinduzidos/genética
Transtornos Autoinduzidos/patologia
Seres Humanos
Masculino
Transtornos Psicóticos/genética
Transtornos Psicóticos/patologia
Dermatopatias Vasculares/genética
Dermatopatias Vasculares/patologia
Adulto Jovem
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE; REVIEW
[Em] Mês de entrada:1710
[Cu] Atualização por classe:171031
[Lr] Data última revisão:
171031
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170402
[St] Status:MEDLINE


  4 / 1406 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
[PMID]:28355139
[Au] Autor:Fredericks C; Yon JR; Alex G; Morton M; Messer T; Bokhari F; Poulakidas S
[Ad] Endereço:Department of General Surgery, Rush University Medical Center, Chicago, IL.
[Ti] Título:Levamisole-induced Necrosis Syndrome: Presentation and Management.
[So] Source:Wounds;29(3):71-76, 2017 Mar.
[Is] ISSN:1943-2704
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Levamisole is an antihelminthic drug with immunomod- ulatory properties. Recent estimates suggest the majority of the cocaine in the United States is adulterated with levamisole. Le- vamisole-induced necrosis syndrome (LINES) is characterized by vasculitis, neutropenia, and purpura that progresses to skin necro- sis. Diagnosis relies on physical examination ndings and history of previous cocaine use. The purpose of this case series is to describe the pathophysiology, diagnosis, and management of LINES. The au- thors' institutional database was reviewed from 2008 to 2015, and they found 3 patients with LINES. Subsequent management and outcomes data are discussed. Patients had a variety of outcomes ranging from local wound care to necrosis and amputation of pha- langes. Patients with LINES can have a wide variety of outcomes; thus, this syndrome must be aggressively managed. Psychotherapy should also be utilized to help patients with further cocaine use. Levamisole-induced necrosis syndrome incidence is expected to in- crease, and all providers should be aware of this patient population.
[Mh] Termos MeSH primário: Transtornos Relacionados ao Uso de Cocaína/terapia
Cocaína/efeitos adversos
Desbridamento/métodos
Levamisol/efeitos adversos
Necrose/induzido quimicamente
Dermatopatias Vasculares/induzido quimicamente
[Mh] Termos MeSH secundário: Adulto
Superfície Corporal
Transtornos Relacionados ao Uso de Cocaína/diagnóstico
Contaminação de Medicamentos
Feminino
Seres Humanos
Levamisol/farmacocinética
Necrose/terapia
Curativos Oclusivos
Guias de Prática Clínica como Assunto
Dermatopatias Vasculares/terapia
Síndrome
Resultado do Tratamento
Cicatrização
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Nm] Nome de substância:
2880D3468G (Levamisole); I5Y540LHVR (Cocaine)
[Em] Mês de entrada:1710
[Cu] Atualização por classe:171020
[Lr] Data última revisão:
171020
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170330
[St] Status:MEDLINE


  5 / 1406 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo
[PMID]:28198027
[Au] Autor:Wee E; Kelly RI
[Ad] Endereço:Department of Dermatology, St Vincent's Hospital Melbourne, VIC, Australia.
[Ti] Título:The histopathology of cutaneous polyarteritis nodosa and its relationship with lymphocytic thrombophilic arteritis.
[So] Source:J Cutan Pathol;44(4):411, 2017 04.
[Is] ISSN:1600-0560
[Cp] País de publicação:United States
[La] Idioma:eng
[Mh] Termos MeSH primário: Arterite
Poliarterite Nodosa
[Mh] Termos MeSH secundário: Dermatite
Seres Humanos
Linfócitos
Dermatopatias Vasculares
[Pt] Tipo de publicação:LETTER; COMMENT
[Em] Mês de entrada:1708
[Cu] Atualização por classe:170817
[Lr] Data última revisão:
170817
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170216
[St] Status:MEDLINE
[do] DOI:10.1111/cup.12901


  6 / 1406 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo
[PMID]:28161822
[Au] Autor:Ramelli V; Lava SA; Simonetti GD; Bianchetti MG; Ramelli GP; Milani GP
[Ad] Endereço:Pediatric Department of Southern Switzerland, 6500, Bellinzona, Switzerland.
[Ti] Título:Blistering eruptions in childhood Henoch-Schönlein syndrome: systematic review of the literature.
[So] Source:Eur J Pediatr;176(4):487-492, 2017 Apr.
[Is] ISSN:1432-1076
[Cp] País de publicação:Germany
[La] Idioma:eng
[Ab] Resumo:The occurrence of blistering eruptions in childhood Henoch-Schönlein syndrome has been so far addressed exclusively in individual case reports. To describe epidemiology, clinical presentation, and therapeutic options in Henoch-Schönlein patients ≤18 years of age with blistering eruptions, we completed a systematic literature search. For the final analysis, we retained 39 reports. Ten children with blisters were found in 7 (1.5%) case series containing a total of 666 unselected pediatric Henoch-Schönlein cases. We also found 41 individually documented cases of Henoch-Schönlein syndrome with blistering eruptions. Blistering eruptions and purpura were distributed very similarly, blisters developed concomitantly with palpable purpura or with a latency of ≤14 days, and 80% of the cases remitted within 4 weeks with a similar course in children managed expectantly and in those managed with steroids. CONCLUSION: Blistering eruptions are rare in Henoch-Schönlein syndrome. They can be a source of diagnostic dilemma but do not have any prognostic value since they almost always spontaneously subside within 4 weeks. What is known: • Textbooks and reviews marginally refer to the occurrence of blistering eruptions in children with Henoch-Schönlein syndrome. What is new • Blistering eruptions occur in <2% of cases. • Blisters and purpura are distributed similarly, blisters develop concomitantly with purpura or with a latency of ≤14 days. • Almost all cases remit within 4 weeks with a similar course in children managed expectantly and in those managed with systemic steroids.
[Mh] Termos MeSH primário: Vesícula/etiologia
Púrpura de Schoenlein-Henoch/complicações
[Mh] Termos MeSH secundário: Vesícula/diagnóstico
Vesícula/epidemiologia
Criança
Feminino
Seres Humanos
Masculino
Púrpura de Schoenlein-Henoch/tratamento farmacológico
Dermatopatias Vasculares/diagnóstico
Dermatopatias Vasculares/tratamento farmacológico
Esteroides/uso terapêutico
[Pt] Tipo de publicação:JOURNAL ARTICLE; REVIEW
[Nm] Nome de substância:
0 (Steroids)
[Em] Mês de entrada:1709
[Cu] Atualização por classe:171006
[Lr] Data última revisão:
171006
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170206
[St] Status:MEDLINE
[do] DOI:10.1007/s00431-017-2858-3


  7 / 1406 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo
[PMID]:28053275
[Au] Autor:Kronbichler A; Leierer J; Leierer G; Mayer G; Casian A; Höglund P; Westman K; Jayne D; European Vasculitis Society
[Ad] Endereço:Vasculitis and Lupus Clinic, Addenbrooke's Hospital, Cambridge, UK.
[Ti] Título:Clinical associations with venous thromboembolism in anti-neutrophil cytoplasm antibody-associated vasculitides.
[So] Source:Rheumatology (Oxford);56(5):704-708, 2017 May 01.
[Is] ISSN:1462-0332
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:Objective.: To assess potential associations for the development of venous thromboembolic events in patients with ANCA-associated vasculitides (AAV). Methods.: Four hundred and seventeen patients enrolled to participate in randomized controlled trials conducted by the European Vasculitis Society were identified. Univariate and multivariate analyses were performed to validate previously proposed and identify novel risks associated with venous thromboembolism (VTE) in AAV. Results.: VTE occurred in 41 of 417 (9.8%) patients. Uncorrected univariate analysis identified BVAS (odds ratio, OR = 1.05, 95% CI: 1.01, 1.10; P = 0.013), subsequent development of malignancy (OR = 2.6, 95% CI: 1.19, 5.71; P = 0.017), mucous membrane or eye involvement (OR = 2.13, 95% CI: 1.10, 4.11; P = 0.024) and baseline creatinine (OR = 1.08, 95% CI: 0.99, 1.18; P = 0.037) as being associated with the development of VTE. Multivariate analysis highlighted CRP (per 10 mg/l increase, OR = 1.05, 95% CI: 1.01, 1.09; P = 0.025), cutaneous involvement (OR = 4.83, 95% CI: 1.63, 14.38; P = 0.005) and gastrointestinal involvement (OR = 6.27, 95% CI: 1.34, 29.37; P = 0.02) among the BVAS items as well as baseline creatinine (per 100 µmol/l increase, OR = 1.17, 95% CI: 1.02, 1.35; P = 0.029) as being associated with VTEs. Conclusion.: Our results highlight a role of CRP, baseline creatinine, and cutaneous and gastrointestinal involvement in the risk stratification as being associated with thromboembolic events. Moreover, there might be an association between VTEs and subsequent development of malignancy and disease activity in general.
[Mh] Termos MeSH primário: Vasculite Associada a Anticorpo Anticitoplasma de Neutrófilos/complicações
Tromboembolia Venosa/etiologia
[Mh] Termos MeSH secundário: Idoso
Proteína C-Reativa/fisiologia
Creatinina/metabolismo
Oftalmopatias/etiologia
Feminino
Gastroenteropatias/etiologia
Seres Humanos
Masculino
Meia-Idade
Membrana Mucosa
Neoplasias/etiologia
Neutrófilos/imunologia
Fatores de Risco
Dermatopatias Vasculares/etiologia
Trombose Venosa/etiologia
[Pt] Tipo de publicação:JOURNAL ARTICLE; MULTICENTER STUDY; RANDOMIZED CONTROLLED TRIAL
[Nm] Nome de substância:
9007-41-4 (C-Reactive Protein); AYI8EX34EU (Creatinine)
[Em] Mês de entrada:1708
[Cu] Atualização por classe:170821
[Lr] Data última revisão:
170821
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:170106
[St] Status:MEDLINE
[do] DOI:10.1093/rheumatology/kew465


  8 / 1406 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo
[PMID]:27938815
[Au] Autor:Kazandjieva J; Antonov D; Kamarashev J; Tsankov N
[Ad] Endereço:Department of Dermatology and Venereology, Medical University Sofia, Sofia, Bulgaria. Electronic address: janaderm@abv.bg.
[Ti] Título:Acrally distributed dermatoses: Vascular dermatoses (purpura and vasculitis).
[So] Source:Clin Dermatol;35(1):68-80, 2017 Jan - Feb.
[Is] ISSN:1879-1131
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Purpuric lesions appear in acral distribution in a variety of conditions and often provide clues to the clinical diagnosis. Purpuric means "hemorrhagic"-that is, the lesions do not blanch from pressure. This review focuses on dermatoses that produce hemorrhagic lesions in acral distribution from the large groups of the vasculitic diseases and their mimics. Cutaneous small vessel vasculitis is confined to the skin, involves mainly postcapillary venules, and has the hallmark manifestation of palpable purpura. Henoch-Schönlein purpura is an immune complex-mediated systemic vasculitis of the small vessels with manifestations from the skin, joints, kidneys, and gastrointestinal system. Only cases where the immune complexes contain immunoglobulin A type are classified as Henoch-Schönlein purpura. Cryoglobulinemic vasculitis is induced by the deposition of cold-precipitated immune complexes in the small vessels. Urticarial vasculitis comprises a spectrum of conditions with the characteristic course of chronic urticaria, with wheals that persist longer than 24 hours, leave hyperpigmentation, and have leukocytoclastic vasculitis on histologic examination. Polyarteritis nodosa is a rare multisystem, segmental necrotizing vasculitis of mainly the medium-sized vessels. Pigmented purpuric dermatoses are chronic benign dermatoses characterized by petechiae, purpura, and increased skin pigmentation. The hallmark of pigmented purpuric dermatoses is their orange-brown, speckled, cayenne pepper-like discoloration.
[Mh] Termos MeSH primário: Dermatoses do Pé/etiologia
Dermatoses da Mão/etiologia
Dermatoses da Perna/etiologia
Púrpura/complicações
Dermatopatias Vasculares/complicações
Vasculite/complicações
[Mh] Termos MeSH secundário: Braço
Síndrome de Churg-Strauss/complicações
Síndrome de Churg-Strauss/patologia
Embolia/complicações
Granulomatose com Poliangiite/complicações
Seres Humanos
Transtornos da Pigmentação/complicações
Transtornos da Pigmentação/diagnóstico
Transtornos da Pigmentação/patologia
Poliarterite Nodosa/complicações
Poliarterite Nodosa/patologia
Púrpura/diagnóstico
Púrpura/patologia
Púrpura Fulminante/complicações
Púrpura de Schoenlein-Henoch/complicações
Púrpura de Schoenlein-Henoch/diagnóstico
Púrpura de Schoenlein-Henoch/terapia
Vasculite/diagnóstico
Vasculite/tratamento farmacológico
Vasculite/patologia
[Pt] Tipo de publicação:JOURNAL ARTICLE; REVIEW
[Em] Mês de entrada:1706
[Cu] Atualização por classe:170620
[Lr] Data última revisão:
170620
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:161213
[St] Status:MEDLINE


  9 / 1406 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
[PMID]:27787337
[Au] Autor:Demirkesen C
[Ad] Endereço:Department of Pathology, Acibadem University, Istanbul, Turkey.
[Ti] Título:Approach to cutaneous vasculitides with special emphasis on small vessel vasculitis: histopathology and direct immunofluorescence.
[So] Source:Curr Opin Rheumatol;29(1):39-44, 2017 Jan.
[Is] ISSN:1531-6963
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:PURPOSE OF REVIEW: The present review will focus on recent publications in cutaneous vasculitides. RECENT FINDINGS: Some histopathological and clinical features, such as papillary dermal edema, perivascular C3 deposition, clinically evident edema, and lesions above the waist, may point out renal or gastrointestinal involvement in Henoch-Schönlein purpura (HSP). HSP associated with familial Mediterranean fever differs from typical isolated HSP by showing no deposits of IgA, much younger age, and location of the lesions on the face or the trunk. Single-organ cutaneous small vessel vasculitis is a more restricted entity than hypersensitivity vasculitis and HSP. Because cutaneous polyarteritis nodosa and macular lymphocytic arteritis share some clinicopathologic features, the question is raised whether they are not two different entities. Several histopathological features defining IgG4-related disease are found in granuloma faciale and erythema elevatum diutinum, two localized chronic cutaneous vasculitis; however, in a recent series no diagnostic criteria for IgG4-related disease was detected in them. SUMMARY: When a patient presents with skin lesions, in which necrotizing or leukocytoclastic vascuitis is confirmed histologically, irrespective of the size of the affected vessel, the possibility of systemic vasculitis, an infection, medication, or a systemic disease such as systemic lupus erythematosus must be searched before reaching definitive diagnosis.
[Mh] Termos MeSH primário: Dermatopatias Vasculares/patologia
Vasculite/patologia
[Mh] Termos MeSH secundário: Arterite/diagnóstico
Arterite/imunologia
Arterite/patologia
Técnica Direta de Fluorescência para Anticorpo/métodos
Seres Humanos
Imunoglobulina G/sangue
Poliarterite Nodosa/diagnóstico
Poliarterite Nodosa/imunologia
Poliarterite Nodosa/patologia
Púrpura de Schoenlein-Henoch/diagnóstico
Púrpura de Schoenlein-Henoch/imunologia
Púrpura de Schoenlein-Henoch/patologia
Dermatopatias Vasculares/diagnóstico
Dermatopatias Vasculares/imunologia
Vasculite/diagnóstico
Vasculite/imunologia
Vasculite Leucocitoclástica Cutânea/diagnóstico
Vasculite Leucocitoclástica Cutânea/imunologia
Vasculite Leucocitoclástica Cutânea/patologia
[Pt] Tipo de publicação:JOURNAL ARTICLE; REVIEW
[Nm] Nome de substância:
0 (Immunoglobulin G)
[Em] Mês de entrada:1707
[Cu] Atualização por classe:170703
[Lr] Data última revisão:
170703
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:161028
[St] Status:MEDLINE


  10 / 1406 MEDLINE  
              first record previous record
seleciona
para imprimir
Fotocópia
Texto completo
[PMID]:27748264
[Au] Autor:Chikazawa S; Hanafusa T; Ozaki K; Namiki T; Amano M; Ueno M; Tokoro S; Igawa K; Sato T; Ishikawa K; Yokota T; Yokozeki H
[Ad] Endereço:Department of Dermatology.
[Ti] Título:Incomplete Behçet's disease with calf muscle pain and MRI hyperintensity due to possible thrombophlebitis.
[So] Source:Eur J Dermatol;27(1):76-77, 2017 Feb 01.
[Is] ISSN:1952-4013
[Cp] País de publicação:France
[La] Idioma:eng
[Mh] Termos MeSH primário: Síndrome de Behçet/complicações
Músculo Esquelético/diagnóstico por imagem
Mialgia/etiologia
Miosite/diagnóstico
Dermatopatias Vasculares/etiologia
Tromboflebite/diagnóstico por imagem
[Mh] Termos MeSH secundário: Adolescente
Diagnóstico Diferencial
Seres Humanos
Perna (Membro)
Imagem por Ressonância Magnética
Masculino
Tromboflebite/etiologia
[Pt] Tipo de publicação:CASE REPORTS; LETTER
[Em] Mês de entrada:1710
[Cu] Atualização por classe:171016
[Lr] Data última revisão:
171016
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:161018
[St] Status:MEDLINE
[do] DOI:10.1684/ejd.2016.2892



página 1 de 141 ir para página                         
   


Refinar a pesquisa
  Base de dados : MEDLINE Formulário avançado   

    Pesquisar no campo  
1  
2
3
 
           



Search engine: iAH v2.6 powered by WWWISIS

BIREME/OPAS/OMS - Centro Latino-Americano e do Caribe de Informação em Ciências da Saúde