Chest
Volume 66, Issue 5, November 1974, Pages 590-594
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Selected Reports
Systemic-to-Pulmonary Fistula in Intrapulmonary Hodgkin's Disease

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Review of the Literature

Burchell and Clagett1 presented the first case of a pulmonary arteriovenous fistula with collateral circulation involving the thoracic wall. Six additional reports of systemic-to-pulmonary fistulae involving chest wall vessels were found in the English literature.2, 3, 4, 5, 6, 7

Pulmonary arteriovenous fistulae may be either congenital or acquired in origin, the former being the most common. Of the seven reported cases involving chest wall vessels, five were felt to be congenital and two

Case Report

A 36-year-old physician had experienced good health until two months prior when he developed generalized myalgia, malaise, and a flulike syndrome, which improved with rest. One month later he developed a cough with only slight production of sputum, pleuritic pain of the left anterior chest, with underlying tenderness of the chest wall and temperature elevation. Self-auscultation of the chest at that time revealed a continuous murmur over the left anterior chest which had not been present on

Discussion

Pulmonary arteriovenous fistulae may result in either right-to-left or left-to-right shunting of blood. With the rare occurrence of systemic chest wall vessel involvement, ie, internal mammary and/or intercostal arteries, the higher pressure systemic circulation may result in a left-to-right shunt with little clinical manifestation, depending on the size of the shunt. Table 1 summarizes the findings of the reported cases of systemic-to-pulmonary arteriovenous fistulae. Only two of the patients

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