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1.
J Pediatr ; 137(4): 578-80, 2000 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-11035843

RESUMO

We describe 10 patients who developed a psoriatic skin eruption during either the acute or convalescent phase of Kawasaki disease. The skin eruption was pustular in 3 patients, but more typical psoriasiform skin lesions were seen in the remaining 7 patients. No patient has yet developed chronic psoriasis.


Assuntos
Síndrome de Linfonodos Mucocutâneos/complicações , Psoríase/etiologia , Doença Aguda , Criança , Pré-Escolar , Humanos , Lactente
2.
J Pediatr ; 128(5 Pt 1): 701-3, 1996 May.
Artigo em Inglês | MEDLINE | ID: mdl-8627447

RESUMO

Although gastrointestinal hemorrhage is a well-recognized complication of aspirin therapy, this side effect has not been previously reported in patients with Kawasaki disease (KD). We describe two children with typical KD who had massive gastrointestinal bleeding that required hospitalization and transfusion. Physicians caring for patients with KD should instruct parents on the signs and symptoms of aspirin toxicity. Fortunately, gastrointestinal hemorrhage appears to be a rare complication of salicylate therapy in patients with Kawasaki disease.


Assuntos
Aspirina/efeitos adversos , Hemorragia Gastrointestinal/induzido quimicamente , Síndrome de Linfonodos Mucocutâneos/tratamento farmacológico , Doença Aguda , Pré-Escolar , Cimetidina/uso terapêutico , Transfusão de Eritrócitos , Feminino , Hemorragia Gastrointestinal/sangue , Hemorragia Gastrointestinal/terapia , Humanos , Masculino , Síndrome de Linfonodos Mucocutâneos/fisiopatologia , gama-Globulinas/uso terapêutico
3.
J Pediatr ; 123(4): 657-9, 1993 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-8410524

RESUMO

We retrospectively reviewed the effects of intravenous gamma-globulin (IVGG) re-treatment of 13 children with Kawasaki disease and persistent or recrudescent fever. Fever and mucocutaneous inflammation resolved within 48 hours in nine patients; fever abated in two other children after a third course of IVGG. We conclude that IVGG re-treatment of Kawasaki disease appears to be safe and may improve the clinical course.


Assuntos
Imunoglobulinas Intravenosas/uso terapêutico , Síndrome de Linfonodos Mucocutâneos/terapia , Pré-Escolar , Feminino , Humanos , Masculino , Síndrome de Linfonodos Mucocutâneos/epidemiologia , Estudos Retrospectivos , Falha de Tratamento
4.
J Pediatr ; 120(3): 376-80, 1992 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-1538283

RESUMO

Because Kawasaki disease is a disorder characterized by lymphocyte activation and immune complex destruction of endothelial cells, we examined the effect of administration of high doses of intravenously administered immune globulin (IVIG) on a lymphocyte population with affinity for endothelial cells: the natural killer cells. We found that administration of high doses of IVIG resulted in a significant increase in the activity of natural killer cells and in the numbers of circulating CD16+ cells. Furthermore, a study of patients treated with IVIG for seizure disorders suggests that this effect of IVIG on circulating NK cells is not unique to patients with Kawasaki disease. The beneficial effect of IVIG in the treatment of Kawasaki disease may be due to the ability of IVIG to inhibit interaction between natural killer cells and endothelial cells.


Assuntos
Imunoglobulinas Intravenosas/imunologia , Células Matadoras Naturais/imunologia , Citotoxicidade Celular Dependente de Anticorpos , Criança , Epilepsia/imunologia , Humanos , Imunoglobulina G/análise , Imunoglobulinas Intravenosas/administração & dosagem , Síndrome de Linfonodos Mucocutâneos/imunologia
5.
J Pediatr ; 118(5): 680-6, 1991 May.
Artigo em Inglês | MEDLINE | ID: mdl-2019921

RESUMO

STUDY OBJECTIVES: (1) To determine those diseases that most often mimic Kawasaki disease (KD) in the United States. (2) To examine the physical findings and laboratory studies that influenced experienced clinicians to exclude the diagnosis of KD. (3) To compare epidemiologic features of patients with KD and patients referred for evaluation of possible KD in whom alternative diagnoses were established. DESIGN: Case comparison study. SETTING: Seven pediatric tertiary care centers. PATIENTS: Consecutive sample of 280 patients with KD and 42 comparison patients examined within the first 14 days after onset of fever. MEASUREMENTS AND MAIN RESULTS: (1) Infectious diseases, particularly measles and group A beta-hemolytic streptococcal infection, most closely mimicked KD and accounted for 35 (83%) of 42 patients in the comparison group. (2) The standard diagnostic clinical criteria for KD were fulfilled in 18 (46%) of 39 patients in whom other diagnoses were established. (3) Patients with KD were significantly less likely to have exudative conjunctivitis or pharyngitis, generalized adenopathy, and discrete intraoral lesions, and more likely to have a perineal distribution of their rash. The patients with KD were also more likely to have anemia and elevated erythrocyte sedimentation rate; leukocyte count less than 10 X 10(3)/mm3 and platelet count less than 200 X 10(3)/mm3 were significantly less prevalent in patients with KD. (4) Residence within 200 yards of a body of water was more common among KD patients. CONCLUSIONS: (1) Measles and streptococcal infection should be excluded in patients examined for possible KD. (2) Laboratory studies that may be useful in discriminating patients with KD from those with alternative diagnoses include hemoglobin concentration, erythrocyte sedimentation rate, and serum alanine aminotransferase activity. (3) Residence near a body of water may be a risk factor for the development of KD.


Assuntos
Síndrome de Linfonodos Mucocutâneos/diagnóstico , Fatores Etários , Criança , Diagnóstico Diferencial , Humanos , Sarampo/diagnóstico , Síndrome de Linfonodos Mucocutâneos/epidemiologia , Exame Físico , Fatores de Risco , Estados Unidos/epidemiologia
6.
J Pediatr ; 118(3): 456-9, 1991 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-1999792

RESUMO

Because patients with Kawasaki disease have low serum concentrations of salicylates despite high doses, and because the free (unbound) drug is responsible for the pharmacologic effects of salicylates, we assessed salicylate protein binding in patients with Kawasaki disease. During the acute phase of the disease, protein binding of salicylate in 36 children with Kawasaki disease was 73 +/- 12%, significantly lower than during the subacute phase (90.4 +/- 8.7%; p less than 0.0005). Mean serum albumin concentration was 29.2 +/- 6.4 gm/L during the acute phase and 36.7 +/- 7.8 gm/L during the subsequent subacute phase (p less than 0.005). Salicylate protein binding was affected independently by both serum albumin and total salicylate levels. During the acute phase of Kawasaki disease, children had an average twofold increase in free salicylate compared with normoalbuminemic control subjects. A nomogram has been devised to derive free salicylate levels from the known total salicylate and serum albumin concentrations.


Assuntos
Síndrome de Linfonodos Mucocutâneos/sangue , Salicilatos/sangue , Albumina Sérica/metabolismo , Doença Aguda , Adulto , Radioisótopos de Carbono , Criança , Humanos , Síndrome de Linfonodos Mucocutâneos/tratamento farmacológico , Ligação Proteica , Salicilatos/administração & dosagem , Salicilatos/análise , Albumina Sérica/análise , Ultrafiltração
7.
J Pediatr ; 117(3): 371-7, 1990 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-2391591

RESUMO

In five children who met the diagnostic criteria for Kawasaki Disease, sensorineural hearing loss developed in association with the acute illness. The children, aged 7 months to 13 years, had deficits ranging from mild to profound bilateral sensorineural hearing loss. There were no associated neurologic abnormalities, and immunologic investigations and magnetic resonance imaging failed to reveal a cause. Treatment regimens differed among the children, but none had high salicylate levels (greater than 20 mg/dl) or received other ototoxic medications. Antiinflammatory therapy was not obviously beneficial in any case, and four of the children have persistent hearing deficits. We conclude that auditory involvement may be a complication of Kawasaki disease; screening of clinically affected children should be considered.


Assuntos
Perda Auditiva Neurossensorial/etiologia , Síndrome de Linfonodos Mucocutâneos/complicações , Adolescente , Antibacterianos/uso terapêutico , Contagem de Células Sanguíneas , Criança , Pré-Escolar , Ecocardiografia , Feminino , Testes Auditivos , Humanos , Lactente , Masculino , Síndrome de Linfonodos Mucocutâneos/tratamento farmacológico
8.
J Pediatr ; 109(5): 759-63, 1986 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-3772656

RESUMO

We report an unselected series of eight patients younger than 6 months of age with Kawasaki disease evaluated between January 1982 and May 1984. The incidence of coronary artery aneurysms (six patients) and the mortality (two patients) were unusually high in this small series. Because of the confusing clinical presentation in three patients, diagnosis was delayed until pathologic or echocardiographic evidence of coronary vasculitis or aneurysm was discovered. The currently accepted clinical criteria for Kawasaki disease may not always identify patients with the pathologic findings of the syndrome who are younger than 6 months of age. The diagnosis of Kawasaki disease and echocardiographic evaluation of the coronary arteries should be considered in young infants with prolonged fever of unknown origin.


Assuntos
Síndrome de Linfonodos Mucocutâneos , Aspirina/administração & dosagem , Aspirina/uso terapêutico , Aneurisma Coronário/diagnóstico , Aneurisma Coronário/etiologia , Aneurisma Coronário/mortalidade , Aneurisma Coronário/patologia , Dipiridamol , Quimioterapia Combinada , Ecocardiografia , Eletrocardiografia , Feminino , Febre/etiologia , Humanos , Lactente , Masculino , Síndrome de Linfonodos Mucocutâneos/diagnóstico , Síndrome de Linfonodos Mucocutâneos/mortalidade , Síndrome de Linfonodos Mucocutâneos/patologia , Miocárdio/patologia , Risco , Varfarina/uso terapêutico
9.
J Pediatr ; 105(2): 206-11, 1984 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-6235335

RESUMO

Prospective evaluation of platelet activation and hypercoagulability was performed in 31 patients with Kawasaki syndrome. Most patients had elevated acute-phase reactants when studied during the first 3 weeks of their illness; 17 of 25 (68%) patients had factor VIII activity greater than 150%, 18 of 24 (75%) had fibrinogen greater than 400 mg/dl, and 17 of 31 (55%) had a platelet count greater than 450,000/mm3. Antithrombin III was depressed initially in 17 of 25 (68%) patients. Depleted fibrinolytic activity, as measured by a euglobulin lysis time greater than 300 minutes, was documented in nine of 20 (45%) patients. Plasma beta-thromboglobulin (BTG) measured at 0 to 3 weeks was elevated (greater than 43 ng/ml) in seven of 24 (29%) patients. All patients with coronary artery aneurysms had elevated BTG values. The mean BTG in the group with aneurysms was 72.3 ng/ml when measured during the first 3 weeks after onset of fever, and 87.7 ng/ml at 4 to 7 weeks. The group without aneurysms had mean BTG values of 29.4 and 28.3 ng/ml at 0 to 3 and 4 to 7 weeks, respectively. The difference between the two groups was significant (P less than 0.002) for both the initial and later values. An elevated BTG during the first 3 weeks after onset of fever was highly associated with aneurysm formation in our patients (P less than 0.007). No aneurysms occurred in patients with a normal BTG value.


Assuntos
Aneurisma/diagnóstico , Transtornos Plaquetários/sangue , Doença das Coronárias/diagnóstico , Coagulação Intravascular Disseminada/sangue , Síndrome de Linfonodos Mucocutâneos/sangue , Aneurisma/etiologia , Antitrombina III/análise , Transtornos Plaquetários/etiologia , Plaquetas/análise , Pré-Escolar , Doença das Coronárias/etiologia , Coagulação Intravascular Disseminada/etiologia , Fibrinogênio/análise , Humanos , Lactente , Síndrome de Linfonodos Mucocutâneos/complicações , Risco , beta-Tromboglobulina/análise
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