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Weil’s syndrome overview

Published: July 17, 2009. Updated: August 09, 2009

Weil's syndrome, is caused by water borne infection by Leptospira icterohemorrhagica and is the most severe form of leptospirosis.

Clinical manifestations

The incubation period is approximately 2 weeks.

The onset of illness is no different from that of less severe leptospirosis with Leptospirosis may present as an acute influenza-like illness, with fever, chills, severe headache, nausea, vomiting, and myalgias. Muscle pain, which especially affects the calves, back, and abdomen, is an important feature of leptospiral infection. However, unlike milder leptospirosis after 9 days, jaundice as well as renal and vascular dysfunction generally develop. Although some degree of defervescence may be noted after the first week of illness, a biphasic disease pattern like that seen in anicteric leptospirosis is lacking. The jaundice of Weil's syndrome, which can be profound and give an orange cast to the skin, is usually not associated with severe hepatic necrosis. Death is rarely due to liver failure. Hepatomegaly and tenderness in the right upper quadrant are usually detected. Splenomegaly is found in 20% of cases.

Renal failure may develop, often during the second week of illness. Hypovolemia and decreased renal perfusion contribute to the development of acute tubular necrosis with oliguria or anuria. Dialysis is sometimes required, although a fair number of cases can be managed without dialysis. Renal function may be completely regained.

Pulmonary involvement occurs frequently, resulting in cough, dyspnea, chest pain, and blood-stained sputum, and sometimes in hemoptysis or even respiratory failure. Hemorrhagic manifestations are seen in Weil's syndrome: epistaxis, petechiae, purpura, and ecchymoses are found commonly, while severe gastrointestinal bleeding and adrenal or subarachnoid hemorrhage are detected rarely.

Rhabdomyolysis, hemolysis, myocarditis, pericarditis, congestive heart failure, cardiogenic shock, adult respiratory distress syndrome, and multiorgan failure have all been described during severe leptospirosis.


A definite diagnosis of leptospirosis is based either on isolation of the organism from the patient or on seroconversion or a rise in antibody titer in the microscopic agglutination test (MAT).


Antimicrobial therapy should be started at once. Intravenous administration of penicillin G, amoxicillin, ampicillin, or erythromycin is recommended.

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