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1.
Hautarzt ; 62(7): 524-33, 2011 Jul.
Artigo em Alemão | MEDLINE | ID: mdl-21647771

RESUMO

Ulcerations of the skin and mucosal membranes are a common feature of autoinflammatory diseases. They can give raise to chronic wound healing defects and should be considered in the differential diagnosis of chronic skin ulcers. The increased activation of the innate immune system in the absence of an apparent provocation for inflammation is a hallmark of autoinflammatory diseases. Mutations and alterations of signaling pathways regulating the innate immune response to physical trauma/tissue damage result into an unrestrained activation of the inflammasome, which leads to increased activation of Interleukin-1. Uncontrolled recruitment and activation of myeloid effector cells within the wound site lead to the release of potent proteases that cause the degradation of structural components of the skin. The majority of these diseases respond well to immunosuppressive and immunomodulatory treatment regimes. Therapeutic resistance converts the acute inflammatory response into a chronic and non-resolving inflammatory process that leads to tissue degeneration. In this article we will focus on the review of those autoinflammatory diseases that often display ulcerative cutaneous and aphthous lesions including pyoderma gangrenosum, Behçet disease, PAPA syndrome and hyperimmunoglobulinemia D with periodic fever syndrome (HIDS). Furthermore, the article will be complemented by an overview of those inflammatory diseases that are associated with non-ulcerative cutaneous manifestations.


Assuntos
Doenças Hereditárias Autoinflamatórias/diagnóstico , Úlcera Cutânea/diagnóstico , Cicatrização/imunologia , Acne Vulgar/diagnóstico , Acne Vulgar/tratamento farmacológico , Acne Vulgar/genética , Acne Vulgar/imunologia , Artrite Infecciosa/diagnóstico , Artrite Infecciosa/tratamento farmacológico , Artrite Infecciosa/genética , Artrite Infecciosa/imunologia , Síndrome de Behçet/diagnóstico , Síndrome de Behçet/tratamento farmacológico , Síndrome de Behçet/genética , Síndrome de Behçet/imunologia , Análise Mutacional de DNA , Diagnóstico Diferencial , Doenças Hereditárias Autoinflamatórias/tratamento farmacológico , Doenças Hereditárias Autoinflamatórias/genética , Doenças Hereditárias Autoinflamatórias/imunologia , Humanos , Fatores Imunológicos/uso terapêutico , Imunossupressores/uso terapêutico , Inflamassomos/sangue , Interleucina-1/sangue , Deficiência de Mevalonato Quinase/diagnóstico , Deficiência de Mevalonato Quinase/tratamento farmacológico , Deficiência de Mevalonato Quinase/genética , Deficiência de Mevalonato Quinase/imunologia , Pioderma Gangrenoso/diagnóstico , Pioderma Gangrenoso/tratamento farmacológico , Pioderma Gangrenoso/genética , Pioderma Gangrenoso/imunologia , Úlcera Cutânea/tratamento farmacológico , Úlcera Cutânea/genética , Úlcera Cutânea/imunologia , Estomatite Aftosa/diagnóstico , Estomatite Aftosa/genética , Estomatite Aftosa/imunologia , Cicatrização/efeitos dos fármacos
2.
Hautarzt ; 58(11): 939-44, 2007 Nov.
Artigo em Alemão | MEDLINE | ID: mdl-17909730

RESUMO

Underlying disease may impair normal wound healing, leading to chronic, poorly healing wounds. Efficient treatment strategies require identification and treatment of the underlying disease as well as directed correction of the wound healing defect. A thorough knowledge of tissue repair mechanisms at the cellular and molecular level will help to achieve these goals. This review focuses on new developments in wound healing research and the resulting non-operative therapeutic implications.


Assuntos
Cicatrização , Ferimentos e Lesões/terapia , Pesquisa Biomédica , Western Blotting , Doença Crônica , Previsões , Humanos , Mediadores da Inflamação/fisiologia , Úlcera da Perna/fisiopatologia , Úlcera da Perna/terapia , Mutação , Cicatrização/genética , Cicatrização/fisiologia , Ferimentos e Lesões/tratamento farmacológico , Ferimentos e Lesões/genética , Ferimentos e Lesões/metabolismo , Ferimentos e Lesões/fisiopatologia
3.
Hautarzt ; 55(1): 74-6, 2004 Jan.
Artigo em Alemão | MEDLINE | ID: mdl-14749868

RESUMO

A 60-year-old male athlete developed a folliculitis in the beard region after several competitions. After identification of herpes simplex antigen within the lesions, systemic therapy with acyclovir led to rapid improvement. In folliculitis resistant to antibiotic and anti-inflammatory therapy, viral and mycotic infections as well as eosinophilic folliculitis should be considered as differential diagnostic possibilities.


Assuntos
Dermatite Perioral/diagnóstico , Dermatoses Faciais/diagnóstico , Foliculite/diagnóstico , Herpes Simples/diagnóstico , Aciclovir/uso terapêutico , Antivirais/uso terapêutico , Conjuntivite Bacteriana/diagnóstico , Dermatite Perioral/tratamento farmacológico , Diagnóstico Diferencial , Progressão da Doença , Dermatoses Faciais/tratamento farmacológico , Foliculite/tratamento farmacológico , Herpes Simples/tratamento farmacológico , Humanos , Masculino , Pessoa de Meia-Idade
4.
Am J Dis Child ; 146(2): 201-7, 1992 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-1733151

RESUMO

Blood flow velocities in the internal carotid arteries were studied with pulsed Doppler in 25 neonatal patients (birth weight range, 2600 to 4100 g) who had extracorporeal membrane oxygenation (ECMO). Time averaged mean systolic, mean diastolic, and mean blood flow velocities were calculated. Five infants had right common carotid artery reconstruction. Blood flow velocities measured in 15 healthy full-term infants were used as controls. Findings during ECMO included the following: (1) forward flow in the right internal carotid artery in 50% of the infants; (2) significant increase in the mean diastolic and the mean flow velocities (48% and 128%, respectively) in the left internal carotid artery when compared with pre-ECMO and control infants' values; (3) the elevation in the mean and the mean diastolic velocities was associated with changes in the PaCO2 and with an increase in the diastolic blood pressure; and (4) forward blood velocities in the right internal carotid artery were comparable with blood velocities in the left internal carotid artery and with the blood velocities of control infants. After ECMO, the mean diastolic velocity in the left internal carotid artery decreased significantly, but it remained elevated when compared with pre-ECMO values. Infants with right common carotid reconstruction had blood velocities in the right internal carotid artery comparable with the simultaneous blood velocities in the left internal carotid artery and to the blood velocities of control infants. Twenty-eight percent of the infants had major neuroanatomic lesions. Right or left preponderance was not noted. No association between blood velocity values in the internal carotid arteries or flow direction and the presence or the absence of brain lesions was noted.


Assuntos
Artéria Carótida Interna/diagnóstico por imagem , Artéria Carótida Interna/fisiologia , Oxigenação por Membrana Extracorpórea , Doenças do Recém-Nascido/fisiopatologia , Velocidade do Fluxo Sanguíneo/fisiologia , Encefalopatias/fisiopatologia , Circulação Cerebrovascular/fisiologia , Humanos , Recém-Nascido , Doenças do Recém-Nascido/diagnóstico por imagem , Doenças do Recém-Nascido/terapia , Ultrassonografia
5.
J Thorac Cardiovasc Surg ; 99(4): 735-40, 1990 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-2319797

RESUMO

Extracorporeal circulation and hemoseparation may lead to coupled mechanical and chemical blood trauma and thus influence red cell deformability. Ten patients with coronary artery disease underwent coronary bypass. Patients' blood samples were drawn preoperatively, after extracorporeal circulation, and after hemoseparation. Ten healthy adults served as control subjects. Red blood cell deformability was determined by direct microscopic observation of red blood cells subjected to shear stresses of 1.2 to 13.3 Pa with a counter-rotating rheoscope. Red cell membrane proteins were separated by one-dimensional polyacrylamide gel electrophoresis in the presence of sodium dodecyl sulfate. At 1.2 Pa, preoperative red cell deformability was significantly greater in patients with coronary artery disease than in control subjects. Neither extracorporeal circulation nor hemoseparation changed red cell deformability significantly. Electrophoretic separation of membrane proteins failed to show any quantitative or qualitative differences between patients and control subjects. Moreover RBC membrane proteins of red blood cells in the patients were not altered as a result of extracorporeal circulation or hemoseparation. The preoperatively increased red cell deformability in the patients may be drug-induced. Our data suggest that the extracorporeal circulation and hemoseparation techniques used in this study do not lead to red blood cell damage.


Assuntos
Separação Celular , Doença das Coronárias/sangue , Deformação Eritrocítica , Circulação Extracorpórea , Transfusão de Sangue Autóloga , Doença das Coronárias/cirurgia , Índices de Eritrócitos , Humanos
6.
Eur J Pediatr ; 146(4): 354-9, 1987 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-3308466

RESUMO

Invasive bacterial eye infections in the neonate range from perforating keratitis to panophthalmitis. These infections have gained clinical and therapeutic importance since mortality rates are high and prognosis concerning preservation of vision is poor. Effective antibiotics against the infective agents are now available. Risk factors for developing invasive bacterial eye infections are mainly prematurity and colonisation with Pseudomonas aeruginosa.


Assuntos
Infecções Bacterianas/diagnóstico , Endoftalmite/diagnóstico , Conjuntivite Bacteriana/diagnóstico , Humanos , Recém-Nascido
7.
Monatsschr Kinderheilkd ; 135(2): 112-3, 1987 Feb.
Artigo em Alemão | MEDLINE | ID: mdl-3033476

RESUMO

In a 2-year-old boy the enzyme defect of fructose-1,6-diphosphatase deficiency could be demonstrated in liver tissue, jejunal mucosa and leukocytes. During the neonatal period the boy had suffered from transient metabolic acidosis and hypoglycemia. At the age of 2 years, during a febrile infection, he developed a hyperkinetic-hypotonic syndrome, which disappeared by fructose-free diet and avoidance of prolonged periods of fasting.


Assuntos
Acidose/enzimologia , Amônia/sangue , Erros Inatos do Metabolismo dos Carboidratos/enzimologia , Intolerância à Frutose/enzimologia , Deficiência de Frutose-1,6-Difosfatase , Hipoglicemia/enzimologia , Frutose/administração & dosagem , Intolerância à Frutose/genética , Humanos , Lactente , Masculino
8.
Monatsschr Kinderheilkd ; 134(12): 878-80, 1986 Dec.
Artigo em Alemão | MEDLINE | ID: mdl-3493428

RESUMO

In an eleven year old girl Atrophodermia idiopathica et progressiva Pasini et Pierini, a rare variety of localised scleroderma developed within six months as well outlined, reddish-brown, patchy lesions without induration on her right side. The histological examination revealed perivascular inflammatory infiltrations in all corium layers, and discrete sclerosis radiating into fat tissue cells. The levels of antinuclear antibodies and C-reactive protein were both elevated. During intravenous therapy with penicillin G the skin alterations faded but did not disappear.


Assuntos
Esclerodermia Localizada/patologia , Anticorpos Antinucleares/análise , Biópsia , Proteína C-Reativa/análise , Criança , Feminino , Humanos , Pele/patologia
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