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Chapter 400-500
A. Cough, iron deficiency anemia, infiltrates on chest radiograph B. Clubbing, anemia of chronic disease, bronchiectasis on CT C. Hypoxia, hemoptysis, multiple alveolar infiltrates on chest radiograph D. Hemoptysis, iron deficiency anemia, multiple alveolar infiltrates on chest radiograph E. Respiratory distress, anemia, multiple alveolar infiltrates on chest radiograph
A. pH < 7. 2 B. Bacteria on Gram stain of pleural fluid C. Pleural fluid neutrophils > 100, 000/µL D. Fluid shift on PA → lateral decubitus chest radiograph E. Septations on ultrasound evaluation
A. Pneumothorax B. Right lower lobe pneumonia C. Globular heart D. Subsegmental atelectasis E. Diffuse alveolar infiltrates
A. Asthma B. Pneumonia C. Foreign body D. Esophageal tear E. Dental extraction
A. It is generally present at birth B. It has a 9: 1 male predominance C. It may cause significant psychologic distress D. It typically causes cardiac symptoms in childhood and respiratory symptoms in adulthood E. The Nuss procedure may improve cardiopulmonary symptoms
A. Wheezing—Congestive heart failure B. Chest pain—Pericarditis C. Cyanosis—Anxiety D. Exercise Intolerance—Anemia E. Tachypnea—Metabolic acidosis
A. 1st day of life B. 1st wk of life C. 2nd wk of life D. 1 to 2 mo of age E. 4 mo of age
A. MVP is predominantly congenital but may not be recognized until adolescence or adulthood B. It is common in patients with Marfan syndrome, pectus excavatum, scoliosis, and Ehlers-Danlos syndrome C. Antibiotic prophylaxis is recommended prior to dental procedures D. MVP is associated with premature ventricular contractions E. Specific therapy is not required during childhood
A. Anomaly in arch development B. Anterior displacement of the infundibular septum C. Downward displacement of the tricuspid valve D. Abnormal cardiac looping E. Failure of atrial septum secundum to fuse with the septum primum
A. d-TGA with no associated defects B. l-TGA with no associated defects C. d-TGA with large ASD D. d-TGA with restrictive VSD E. l-TGA with restrictive VSD
A. Anomalous left coronary artery arising from the pulmonary artery B. Hypertrophic cardiomyopathy C. Supraventricular tachycardia D. Atrioventricular canal defect E. Pentology of Cantrell
A. Genotyping may be useful in the diagnosis of asymptomatic family members B. Genotype may predict clinical manifestations in a patient with LQTS C. Genotype may predict a higher risk for sudden death D. Genotype may predict nonresponse to conventional pharmacotherapy E. A negative genotype (i. e., no mutation) may rule out the disorder in suspected cases
A. Aortic B. Mitral C. Pulmonary D. Tricuspid
A. Rhabdomyoma B. Lipoma C. Myxoma D. Fibroma E. Rhabdosarcoma
A. A better prognosis than in older children B. Philadelphia chromosome C. FAB L3 (Burkitt) type D. A translocation involving chromosome 11 E. Spontaneous resolution
A. Hilar lymphadenopathy B. Unilateral cervical adenopathy C. Fever > 39°C D. Pruritus E. Weight loss of 2 kg
A. Acute osteomyelitis B. Chronic osteomyelitis C. Osteoid osteoma D. Ewing sarcoma E. Osteosarcoma
A. Wilms tumor B. Germ cell tumor C. Retinoblastoma D. Rhabdomyosarcoma E. Leiomyosarcoma
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