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Case Report: Coexisting cardiac cavernous hemangioma and sarcoidosis in a single lesion: a first reported case
Chuan-Yong Xiao1,2, Wen-Ya Han1,2, Han-Sheng Wang1,2
1Department of Pulmonary and Critical Care Medicine, Taihe Hospital of Shiyan, Hubei University of Medicine, Shiyan, Hubei, China.
Insights
This report details a rare case of concurrent cardiac hemangioma and cardiac sarcoidosis. A proposed mechanism suggests cardiac sarcoidosis may promote cardiac hemangioma development through microvascular injury.
Area of Science:
- Cardiology
- Oncology
- Pathology
Background:
- Cardiac hemangioma (CH) is a rare benign cardiac tumor with variable manifestations.
- Cardiac sarcoidosis is uncommon, characterized by granulomas and potential cardiac involvement.
- Concurrent CH and cardiac sarcoidosis have not been previously reported.
Abstract:
Cardiac hemangioma (CH) is a rare benign cardiac tumor whose clinical manifestations-including arrhythmias, heart failure, and pericardial effusion-vary by anatomical location. Sarcoidosis is a multisystem disorder of unknown etiology characterized by non-caseating granulomas, commonly involving the lungs, eyes, and skin, with cardiac involvement being relatively uncommon. To date, no cases of concurrent cardiac hemangioma and cardiac sarcoidosis have been reported worldwide. We herein describe a patient with established sarcoidosis who, during follow-up, exhibited progressive enlargement of a cardiac mass. Surgical resection confirmed the co-existence of cardiac hemangioma and cardiac sarcoidosis within the same anatomical region. Based on these findings, we propose a pathophysiological mechanism wherein cardiac sarcoidosis causes microvascular injury, leading to structural alterations that may promote the development of cardiac hemangioma. The following report details the diagnostic and therapeutic course of this patient.

