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Published on: November 18, 2018
Surgical removal of a left ventricular thrombus associated with cardiac sarcoidosis
Shinji Kanemitsu1, Yoichiro Miyake, Manabu Okabe
1Division of Cardiovascular Surgery, Kochi Health Sciences Center, Kochi, Japan. skanemitsu70@yahoo.co.jp
Insights
This study details the successful surgical removal of a rare left ventricular thrombus in a patient with cardiac sarcoidosis. The case highlights surgical intervention for heart failure caused by this uncommon condition.
Area of Science:
- Cardiology
- Cardiovascular Surgery
- Immunology
Background:
- Cardiac sarcoidosis is an inflammatory condition that can lead to heart failure.
- Left ventricular thrombus formation is a known complication of heart failure.
- Surgical management of left ventricular thrombus in cardiac sarcoidosis is exceptionally rare.
Observation:
- A 31-year-old male presented with heart failure secondary to cardiac sarcoidosis.
- Echocardiography revealed diffuse hypokinesis and a mobile, ball-like left ventricular thrombus.
- CT and MRI demonstrated findings suggestive of cardiac sarcoidosis and cerebral infarctions.
Findings:
- Surgical excision of the left ventricular thrombus was successfully performed.
- Pathological examination confirmed non-caseating granulomas, indicative of cardiac sarcoidosis.
- The patient received postoperative treatment with prednisolone for cardiac sarcoidosis.
Implications:
- This case demonstrates the feasibility of surgical intervention for left ventricular thrombus in cardiac sarcoidosis.
- Early diagnosis and multidisciplinary management are crucial for patients with cardiac sarcoidosis.
- Further research may explore optimal treatment strategies for this rare presentation.
Abstract:
We report successful surgical management of a 31-year-old man with a left ventricular thrombus following heart failure due to cardiac sarcoidosis. Preoperative echocardiography showed diffuse hypokinesis and a mobile ball-like thrombus in the left ventricle. Computed tomography revealed a left ventricular tumor and bilateral hilar lymphadenopathy, while MRI of the brain showed small infarctions in the occipital lobe. Postoperative pathologic examination of a specimen from the left ventricular free wall and a mediastinal lymph node revealed non-caseating granulomas consistent with cardiac sarcoidosis. The patient was referred to a cardiologist for further treatment with prednisolone. This is a rare case of surgical removal of a left ventricular ball-like thrombus in a patient with cardiac sarcoidosis.
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