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Published on: February 11, 2022
A Rare Case of Carcinoid Constrictive Pericarditis
Teresa S Wang1, Emily K Bergsland2, Ruth Zhang3
1Division of Cardiology, Department of Medicine, University of California-San Francisco, San Francisco, California.
A rare case of carcinoid heart disease was diagnosed in a patient with metastatic neuroendocrine tumors. The condition, carcinoid-related constrictive pericarditis, presented as pleural effusions and edema.
Area of Science:
- Cardiology
- Oncology
- Pathology
Background:
- Neuroendocrine tumors, particularly atypical carcinoid tumors, can metastasize to distant sites including the liver and lymph nodes.
- Carcinoid heart disease is a rare complication of neuroendocrine tumors, often involving the right heart valves.
- Constrictive pericarditis is a less common manifestation of carcinoid syndrome affecting cardiac function.
Observation:
- A 62-year-old woman with metastatic well-differentiated neuroendocrine tumor presented with recurrent unilateral pleural effusions and lower extremity edema.
- Clinical presentation suggested fluid overload and impaired cardiac function.
- Initial investigations were performed to determine the cause of the patient's symptoms.
Findings:
- Multimodality imaging and comprehensive workup led to the diagnosis of carcinoid-related constrictive pericarditis.
- This diagnosis highlights a rare manifestation of carcinoid heart disease.
- The patient's symptoms were attributed to the pericardial involvement secondary to the neuroendocrine tumor.
Implications:
- This case underscores the importance of considering rare cardiac complications in patients with metastatic neuroendocrine tumors.
- Early diagnosis and management of carcinoid-related constrictive pericarditis are crucial for patient outcomes.
- Further research into the mechanisms and treatment of this rare condition is warranted.
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