Approximately 50% of infections are asymptomatic. The remainder of infections represent either acute lymphatic inflammation or chronic lymphatic obstruction resulting in hydrocele or lymphedema of the limbs.
Acute filariasis is characterized by acute adenolymphangitis, lymphadenitis, and episodic fever ("filarial fever"). Due to chronic lymphatic vessel inflammation and scarring, chronic infection eventually results in primarily asymmetric swelling of the extremities, male genitalia (ie, hydrocele), and breasts in women. Chronic lymphatic disease is rare in children younger than 10 years, but risk increases with age.
Patients from endemic areas may occasionally experience chyluria (milky urine) as renal lymphatics are blocked. Additionally, acute and chronic infection may be associated with tropical pulmonary eosinophilia and peripheral eosinophilia.
The disease course can be prolonged over years to decades.
B74.9 – Filariasis, unspecified
240820001 – Lymphatic filariasis
Differential Diagnosis & Pitfalls
Filarial fever and acute lymphadenopathy must be differentiated from other causes of tropical fevers and lymphadenopathy (eg, bacterial lymphangitis), and common viral infections (eg, influenza, mononucleosis, HIV).
- Podoconiosis (nonfilarial lymphedema) – Usually bilateral and seen in regions with altitudes higher than 1500 meters.
- Other causes of lymphedema, such as congestive heart failure, deep venous thrombosis, and nephrotic syndrome, should be considered.
- Other causes of lymphatic obstruction, such as pelvic tumors, should be considered.