Specialized Programs

 

Myocarditis  

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Myocarditis is inflammation of the heart muscle (myocardium). Myocarditis can result from infection (for example, a virus), autoimmunity (when the immune system attacks one’s own body) as well as drugs including cancer immunotherapies and vaccines. UCSF has developed a center of excellence in myocarditis and other inflammatory cardiovascular diseases. We systematically study these patients and collaborate with other academic centers and industry to develop better diagnostic and treatment strategies for patients.

Myocarditis Center

Filamin C (FLNC)

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Filamin C (FLNC) is a type of filamin protein that is mainly found in skeletal and heart muscle cells, and it helps maintain stability of the muscle. There are some genetic variants (or mutations) that affect the FLNC gene that encodes for filamin C. These mutations can cause abnormal filamin C proteins, which in turn can lead to dysfunction in the heart. The UCSF FLNC Cardiomyopathy program aims to better understand how FLNC variants affect the heart in patients who have these mutations.

Filamin C

Clonal hematopoiesis of indeterminate potential (CHIP)

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Clonal hematopoiesis of indeterminate potential (CHIP) occurs when somatic mutations occur in blood cells. These mutations do not directly cause cancer per say but they do lead to clonal expansion of cells and occur more commonly as patients age and may result in cancer. It is now known that patients with CHIP are especially at risk for heart disease including acute heart attack and stroke. The UCSF CHIP clinic is developing ways to screen for, diagnose and treat CHIP patients.

Cardiac Amyloidosis Program

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Cardiac amyloidosis is an increasingly important but under-recognized heart disease that results from the uncontrolled deposition of amyloid fibrils in the heart. Patients with cardiac amyloidosis can develop progressive heart failure, conduction disease, reduced quality of life, and early mortality.

At the UCSF Cardiac Amyloidosis Program, we offer comprehensive, patient centered care for all forms of cardiac amyloidosis. We have developed protocols for diagnosis, treatment, and monitoring of patients who are referred to our clinic.

Cardiac Amyloidosis Program

Carcinoid Heart Disease­­­­­

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Neuroendocrine tumors (NETs) are rare, slow growing tumors that can be located anywhere in the body, but most commonly occur in the abdomen. These tumors can secrete hormones which can result in patients having specific symptoms such as flushing, diarrhea, and abdominal cramping (carcinoid syndrome). The hormones can also reach the heart and can lead to heart valvular disease. Occasionally patients have minimal symptoms. But, in many cases, the patient may have severe valve disease that can result in heart failure, necessitating valve replacement surgery.

As a part of the UCSF Center for Neuroendocrine Tumors, we work closely with a multi-disciplinary team including oncologists, interventional radiologists and cardiac surgery offering comprehensive evaluation and treatment plans for carcinoid heart disease. 

Hereditary Hemorrhagic Telangiectasia (HHT)

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Hereditary Hemorrhagic Telangiectasia is a genetic disease where patients develop abnormal and fragile blood vessels between arteries and veins (arteriovenous malformations or AVMs). HHT affects approximately 1 and 5000 individuals, and commonly manifests with nosebleeds. Patients with HHT will may also develop AVMs in in the brain, lungs, and/or liver.

Liver AVMs are seen up to 75% of individuals with HHT. Over time, if left unmonitored and untreated, the high output in the circulation may lead to heart failure. As part of the UCSF HHT Center of Excellence, we partner with interventional radiologists, hematologists, and liver specialists designing novel protocols for the diagnosis and management of heart disease in patients with HHT.