Severe Pulmonary Hypertension Without Significant Pulmonary Parenchymal Disease In a Pediatric Patient with Acquired Immunodeficiency Syndome.

Autor: Rhodes, Jonathan, Schiller, Myles S., Montoya, Carlos H., Fikrig, Senih
Předmět:
Zdroj: Clinical Pediatrics; Oct1992, Vol. 31 Issue 10, p629-631, 3p
Abstrakt: The article cites a case study of severe pulmonary hypertension without significant pulmonary parenchymal disease in a pediatric patient with AIDS. Features of this case differ from those of adult AIDS patients and suggest that the natural history and optimal management of pediatric AIDS-related pulmonary hypertension may differ from that of the adult variety. The patient, a child of an intravenous drug abuser, presented at 2 years of age with failure to thrive, adenopathy, hepatosplenomegaly, and chronic impetigo. Serologic testing revealed the presence of HIV infection. At 6 years of age, he developed pneumonia and was successfully treated with antibiotics. Five months later he contracted pneumonia once again. Cardiac examination at that time was remarkable for a 3/6 holosystolic and a 2/6 decrescendo diastolic murmur at the left sternal border, a loud, single second heart sound, and a parasternal heave. Echocardiography revealed marked dilation of the right atrium, right ventricle, and pulmonary artery, in association with tricuspid and pulmonary insufficiency.
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