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Published on: February 8, 2019
Giant cell myocarditis causing sudden death in a patient with sarcoidosis
John P Ziegler1, Nicholas I Batalis2, James W Fulcher3
1Medical University of South Carolina, Charleston, SC, USA.
Insights
Giant cell myocarditis (GCM) is a rare, fatal heart condition. This case highlights GCM
Area of Science:
- Cardiovascular Pathology
- Immunology
- Autopsy Medicine
Background:
- Giant cell myocarditis (GCM) is a rare, aggressive cardiovascular disease.
- It presents with myocardial necrosis and giant cells, often in young adults.
- GCM can manifest as heart failure or sudden cardiac death.
Observation:
- A fatal case of GCM in a 36-year-old male with autoimmune disorders is presented.
- The patient initially presented with non-specific symptoms like vomiting.
- Autopsy revealed findings consistent with psoriasis and pulmonary sarcoidosis.
Findings:
- The case supports a link between GCM and autoimmune disorders.
- Distinguishing GCM from cardiac sarcoidosis (CS) is crucial, especially with systemic sarcoidosis.
- GCM can present atypically, leading to misdiagnosis and delayed treatment.
Implications:
- Increased awareness of GCM is needed for timely diagnosis and intervention.
- Early cardiac transplantation and immunosuppression are key to improving prognosis.
- This case underscores the importance of considering GCM in sudden cardiac death evaluations.
Abstract:
Giant cell myocarditis (GCM) is a rare and rapidly fatal cardiovascular condition most often seen in young adults. It is characterized microscopically by myocardial necrosis with multinucleated giant cells in the absence of well-defined granulomas. This disorder has typically been attributed to manifest as heart failure, but in some individuals, GCM may present as sudden cardiac death. Herein, we present a fatal case of GCM in a 36-year-old male with a history of autoimmune disorders. The decedent presented to the emergency room due to vomiting and was treated for nausea due to suspected dehydration. He was discharged that night and found dead on his bathroom floor the following day. Postmortem examination revealed psoriasis and granulomatous lesions in the lungs consistent with sarcoidosis, further supporting circumstantial evidence existing between GCM and autoimmune disorders. Additionally, this case provides an opportunity to distinguish GCM from the distinct clinical entity of cardiac sarcoidosis (CS), especially in the setting of systemic sarcoidosis. We hope to raise awareness of this rare disease process and its potential to cause sudden cardiac death so that it may be considered in a differential diagnosis as immunosuppression and early cardiac transplantation largely determine the prognosis.
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