Libman–Sacks endocarditis: Difference between revisions

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'''Libman–Sacks endocarditis''' is a form of [[nonbacterial thrombotic endocarditis]] (NBTE) that is seen in association with [[systemic lupus erythematosus]] (SLE). It was first described by the American pathologists [[Emanuel Libman]] and [[Benjamin Sacks]] in 1924.


{{Infobox medical condition
| name            = Libman–Sacks endocarditis
| synonyms        = Nonbacterial thrombotic endocarditis (NBTE)
| field          = [[Cardiology]], [[Rheumatology]]
| symptoms        = Often asymptomatic; may include [[fever]], [[fatigue]], [[shortness of breath]], [[chest pain]]
| complications  = [[Heart failure]], [[stroke]], [[systemic embolism]]
| onset          = Variable
| duration        = Chronic
| causes          = Associated with [[systemic lupus erythematosus]] (SLE), [[antiphospholipid syndrome]]
| risks          = [[Autoimmune disease]], [[hypercoagulable state]]
| diagnosis      = [[Echocardiography]], [[blood tests]]
| differential    = [[Infective endocarditis]], [[rheumatic heart disease]]
| treatment      = Management of underlying condition, [[anticoagulation]]
| prognosis      = Variable, depends on underlying condition
| frequency      = Rare
}}
'''Libman–Sacks endocarditis''' is a form of [[nonbacterial thrombotic endocarditis]] (NBTE) that is seen in association with [[systemic lupus erythematosus]] (SLE). It was first described by the American pathologists [[Emanuel Libman]] and [[Benjamin Sacks]] in 1924.
==Etiology==
==Etiology==
 
The exact cause of Libman–Sacks endocarditis is unknown, but it is closely associated with SLE and [[antiphospholipid syndrome]] (APS). It is thought to be due to the formation of [[autoantibodies]] in these conditions, which cause damage to the [[endothelium]] of the heart valves.
The exact cause of Libman–Sacks endocarditis is unknown, but it is closely associated with SLE and [[antiphospholipid syndrome]] (APS). It is thought to be due to the formation of [[autoantibodies]] in these conditions, which cause damage to the [[endothelium]] of the heart valves.
 
==Pathology==
==Pathology==
 
Libman–Sacks endocarditis is characterized by the presence of sterile vegetations on the heart valves. These vegetations are composed of fibrin and platelets, and are often associated with underlying valve damage. The mitral valve is the most commonly affected, but any valve can be involved.
Libman–Sacks endocarditis is characterized by the presence of sterile vegetations on the heart valves. These vegetations are composed of fibrin and platelets, and are often associated with underlying valve damage. The mitral valve is the most commonly affected, but any valve can be involved.
 
==Clinical features==
==Clinical features==
 
Patients with Libman–Sacks endocarditis may be asymptomatic, or they may present with symptoms of [[heart failure]], [[stroke]], or [[systemic embolism]]. The condition is often discovered incidentally during [[echocardiography]] for other reasons.
Patients with Libman–Sacks endocarditis may be asymptomatic, or they may present with symptoms of [[heart failure]], [[stroke]], or [[systemic embolism]]. The condition is often discovered incidentally during [[echocardiography]] for other reasons.
 
==Diagnosis==
==Diagnosis==
 
The diagnosis of Libman–Sacks endocarditis is made by echocardiography, which shows the characteristic vegetations on the heart valves. [[Blood tests]] may show evidence of SLE or APS.
The diagnosis of Libman–Sacks endocarditis is made by echocardiography, which shows the characteristic vegetations on the heart valves. [[Blood tests]] may show evidence of SLE or APS.
 
==Treatment==
==Treatment==
 
The treatment of Libman–Sacks endocarditis involves managing the underlying SLE or APS. This may include [[immunosuppressive therapy]] and [[anticoagulation]]. In severe cases, [[valve replacement surgery]] may be necessary.
The treatment of Libman–Sacks endocarditis involves managing the underlying SLE or APS. This may include [[immunosuppressive therapy]] and [[anticoagulation]]. In severe cases, [[valve replacement surgery]] may be necessary.
 
==Prognosis==
==Prognosis==
 
The prognosis of Libman–Sacks endocarditis is variable, and depends on the severity of the valve damage and the underlying SLE or APS. With appropriate treatment, the condition can often be managed effectively.
The prognosis of Libman–Sacks endocarditis is variable, and depends on the severity of the valve damage and the underlying SLE or APS. With appropriate treatment, the condition can often be managed effectively.
 
==See also==
==See also==
* [[Endocarditis]]
* [[Endocarditis]]
* [[Systemic lupus erythematosus]]
* [[Systemic lupus erythematosus]]
* [[Antiphospholipid syndrome]]
* [[Antiphospholipid syndrome]]
[[Category:Cardiology]]
[[Category:Cardiology]]
[[Category:Rheumatology]]
[[Category:Rheumatology]]
[[Category:Pathology]]
[[Category:Pathology]]
{{Medicine-stub}}
{{Medicine-stub}}

Latest revision as of 23:41, 3 April 2025


Libman–Sacks endocarditis
Synonyms Nonbacterial thrombotic endocarditis (NBTE)
Pronounce N/A
Specialty N/A
Symptoms Often asymptomatic; may include fever, fatigue, shortness of breath, chest pain
Complications Heart failure, stroke, systemic embolism
Onset Variable
Duration Chronic
Types N/A
Causes Associated with systemic lupus erythematosus (SLE), antiphospholipid syndrome
Risks Autoimmune disease, hypercoagulable state
Diagnosis Echocardiography, blood tests
Differential diagnosis Infective endocarditis, rheumatic heart disease
Prevention N/A
Treatment Management of underlying condition, anticoagulation
Medication N/A
Prognosis Variable, depends on underlying condition
Frequency Rare
Deaths N/A


Libman–Sacks endocarditis is a form of nonbacterial thrombotic endocarditis (NBTE) that is seen in association with systemic lupus erythematosus (SLE). It was first described by the American pathologists Emanuel Libman and Benjamin Sacks in 1924.

Etiology[edit]

The exact cause of Libman–Sacks endocarditis is unknown, but it is closely associated with SLE and antiphospholipid syndrome (APS). It is thought to be due to the formation of autoantibodies in these conditions, which cause damage to the endothelium of the heart valves.

Pathology[edit]

Libman–Sacks endocarditis is characterized by the presence of sterile vegetations on the heart valves. These vegetations are composed of fibrin and platelets, and are often associated with underlying valve damage. The mitral valve is the most commonly affected, but any valve can be involved.

Clinical features[edit]

Patients with Libman–Sacks endocarditis may be asymptomatic, or they may present with symptoms of heart failure, stroke, or systemic embolism. The condition is often discovered incidentally during echocardiography for other reasons.

Diagnosis[edit]

The diagnosis of Libman–Sacks endocarditis is made by echocardiography, which shows the characteristic vegetations on the heart valves. Blood tests may show evidence of SLE or APS.

Treatment[edit]

The treatment of Libman–Sacks endocarditis involves managing the underlying SLE or APS. This may include immunosuppressive therapy and anticoagulation. In severe cases, valve replacement surgery may be necessary.

Prognosis[edit]

The prognosis of Libman–Sacks endocarditis is variable, and depends on the severity of the valve damage and the underlying SLE or APS. With appropriate treatment, the condition can often be managed effectively.

See also[edit]

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