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Massive pericardial effusion causing cardiac tamponade accompanied by elevated CA-125 and thoracic lymphadenopathy in
Taalaibek Kudaiberdiev1, Elmira Tukusheva1, Zhanybek Gaibyldaev1
1Scientific Research Institute of Heart Surgery and Organ Transplantation, Bishkek, Kyrgyzstan.
Insights
This case report details a patient with cardiac sarcoidosis presenting as severe pericardial effusion and cardiac tamponade. The condition mimicked malignancy due to elevated CA-125 levels and enlarged lymph nodes.
Area of Science:
- Cardiology
- Oncology
- Pathology
Background:
- Cardiac sarcoidosis is a rare condition.
- Pericardial effusion and cardiac tamponade are uncommon manifestations.
- This report highlights a unique presentation of cardiac sarcoidosis.
Observation:
- A 51-year-old female presented with symptoms of heart failure and elevated CA-125.
- Diagnostic imaging revealed massive pericardial effusion, cardiac tamponade, and enlarged lymph nodes.
- Histological examination confirmed non-caseating epithelioid granulomas, indicative of sarcoidosis.
Findings:
- The patient had severe pericardial effusion and cardiac tamponade.
- Elevated CA-125 levels mimicked gynecologic malignancy.
- Enlarged pericardial and mediastinal lymph nodes were initially mistaken for a pericardial mass.
Implications:
- Sarcoidosis can present with pericardial effusion and tamponade, mimicking malignancy.
- Elevated CA-125 and lymphadenopathy in sarcoidosis require careful evaluation.
- This case broadens the understanding of cardiac sarcoidosis presentations.
Introduction:
Pericardial effusion and cardiac tamponade are rare manifestations of cardiac sarcoidosis. This is a first case report that describes a patient with severe pericardial effusion and signs of cardiac tamponade with elevated carbohydrate antigen 125 (CA-125) levels, enlarged pericardial (PLN) and mediastinal lymph nodes (MLN), histologically confirmed as sarcoidosis.
Presentation Of Case:
A 51-year-old female patient was admitted with complaints of sickness, shortness of breath on minimal exertion, swelling in lower extremities, and heaviness in right upper abdomen. Patient had diminished heart sounds, peripheral edema and hepatomegaly. She had elevated CA-125 level without gynecologic pathology. There were QRS alternation on ECG and water-bottle configuration on chest-X-ray, severe pericardial effusion, and signs of cardiac tamponade on echocardiography. CT demonstrated massive pericardial effusion, pericardial mass and enlargement of anterior MLN. The patient underwent pericardial drainage with removal of 850 mL of pericardial fluid and excision of enlarged PLN. Histological examination of PLN revealed non-caseating epithelioid cell granulomas. The diagnosis of cardiac sarcoidosis was established. Patient was discharged and 6-month follow-up was uneventful.
Discussion:
There are no reports on association of pericardial effusion, with increased CA-125 level in sarcoidosis, as we established in our patient. Our case is notable by incidental finding of enlarged PLN, mimicking pericardial mass and mediastinal lymphoadenopathy on CT, further confirmed by histological examination of PLN specimen as cardiac sarcoidosis.
Conclusion:
It should be kept in mind that sarcoidosis may present as massive pericardial effusion, with signs of tamponade and pericardial lymphoadenopathy mimicking pericardial mass, mediastinal lymphoadenopathy and elevated CA-125, mimicking malignancy.
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