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1.
Pediatrics ; 122(6): e1231-5, 2008 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-18984649

RESUMO

OBJECTIVE: Associations between pleural and pericardial effusions have been described in malignancy and autoimmune disorders. Bacterial pneumonia is the most frequent cause of parapneumonic effusion; however, knowledge of the relationship between parapneumonic effusion and the presence of pericardial fluid in children is limited. We examined this relationship. METHODS: We performed a retrospective chart review of pediatric patients who were admitted to our institution during a 6-year period with a diagnosis of either parapneumonic effusion or empyema and who had undergone an echocardiogram, a computed tomography scan of the thorax, or both. All demographic, clinical, radiographic, and laboratory data of these patients were collected, and statistical analysis was done with Student's t tests and chi2 analyses. RESULTS: We reviewed the charts of 59 children with parapneumonic effusions. Forty-eight underwent 2-dimensional echocardiography, chest computed tomography scan, or both. Of these 48 patients, 54.2% (n=26) were found to have a concomitant pericardial effusion. The majority of patients with pericardial effusions had left-sided pleural disease. Patients with pericardial effusions had more symptomatic days before hospitalization, lower pleural fluid albumin levels, elevated serum white blood cell counts, elevated pleural fluid white blood cell and absolute neutrophil counts, and an increased incidence of surgical intervention. One patient had evidence of hemodynamic compromise that required pericardiocentesis. CONCLUSIONS: We found a high incidence of pericardial effusions in pediatric patients with parapneumonic effusions. Leukocytosis, higher pleural fluid leukocyte and neutrophil counts, and a propensity for surgical intervention suggest a prognostic relationship between pericardial effusions and more severe parapneumonic disease. The majority of these pericardial collections resolve with treatment of the underlying pleural disease.


Assuntos
Derrame Pericárdico/diagnóstico , Derrame Pericárdico/epidemiologia , Derrame Pleural/diagnóstico , Derrame Pleural/epidemiologia , Adolescente , Distribuição por Idade , Criança , Pré-Escolar , Estudos de Coortes , Comorbidade , Drenagem/métodos , Ecocardiografia Transesofagiana , Feminino , Seguimentos , Humanos , Incidência , Lactente , Recém-Nascido , Imageamento por Ressonância Magnética , Masculino , Derrame Pericárdico/terapia , Pericardiocentese/métodos , Derrame Pleural/terapia , Estudos Retrospectivos , Medição de Risco , Índice de Gravidade de Doença , Distribuição por Sexo , Cirurgia Torácica Vídeoassistida/métodos , Tomografia Computadorizada por Raios X
2.
Clin Imaging ; 31(4): 264-8, 2007.
Artigo em Inglês | MEDLINE | ID: mdl-17599621

RESUMO

Pulmonary hyalinizing granulomata are rare, noninfectious, fibrosing lesions of the lung, which can mimic metastatic disease radiographically. Their etiology is unknown, but they may be caused by an exaggerated immune response. We report the radiology, long clinical course, and pathology of a patient with pulmonary hyalinizing granuloma who presented with initially asymptomatic pulmonary nodules. Over a 10-year period, the patient developed multiple insidious autoimmune phenomena, including lupus anticoagulant, neuromyotonia, demyelinating sensorimotor polyneuropathy, and eventually, Morvan's syndrome. Such an association has not been previously published to our knowledge.


Assuntos
Granuloma do Sistema Respiratório/fisiopatologia , Hialina , Inibidor de Coagulação do Lúpus/metabolismo , Evolução Fatal , Granuloma do Sistema Respiratório/diagnóstico por imagem , Humanos , Estudos Longitudinais , Masculino , Pessoa de Meia-Idade , Síndrome , Tomografia Computadorizada por Raios X
4.
Clin Imaging ; 30(2): 132-6, 2006.
Artigo em Inglês | MEDLINE | ID: mdl-16500545

RESUMO

Rhabdoid tumor of the kidney (RTK) is a rare pediatric malignancy. Its imaging features by ultrasound and CT have been well described; however, to our knowledge, there are only a handful of case reports that describe the MR appearance of rhabdoid tumor. We report the MR appearance of a RTK in an 18-month-old boy, review the literature on its imaging features, and discuss the differential diagnosis of solid renal tumors in children.


Assuntos
Neoplasias Renais/diagnóstico , Tumor Rabdoide/diagnóstico , Diagnóstico por Imagem , Humanos , Lactente , Neoplasias Renais/patologia , Neoplasias Renais/cirurgia , Masculino , Estadiamento de Neoplasias , Tumor Rabdoide/patologia , Tumor Rabdoide/cirurgia
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