Tropical pulmonary eosinophilia (TPE) usually affects people living in
the tropics, especially those in Southeast Asia, India, and certain p
arts of China and Africa. However, owing to the rising frequency of wo
rld-wide travel and the migration between continents, this disease is
increasingly seen in the West, where the diagnosis can be easily misse
d since it is rarely encountered and can mimic many other conditions.
Cases of TPE have typically been reported to masquerade as acute or re
fractory bronchial asthma. TPE results from a hypersensitivity reactio
n to lymphatic filarial parasites found in endemic regions. There is e
vidence that it is more likely to occur in nonimmune individuals, ie,
visitors to endemic regions, than in individuals of endemic population
s who have developed immunity to filarial infections. Clinical feature
s include paroxysmal cough, wheezing and dyspnea, and systemic manifes
tations such as fever and weight loss. A history of residence in a fil
arial endemic region and a finding of peripheral eosinophilia > 3,000/
mm(3) should initiate a consideration of this disease. Other criteria
for the diagnosis of TPE include absence of microfilariae in the blood
, high titers of antifilarial antibodies, raised serum total IgE > 1,0
00 U/mL, and a favorable response to the antifilarial, diethylcarbamaz
ine, which is the recommended treatment. This disease, if left untreat
ed or treated late, may lead to long-term sequelae of pulmonary fibros
is or chronic bronchitis with chronic respiratory failure. Herein lies
the importance of early diagnosis and treatment of TPE.