Abstract 4366953: When the Pleural Effusion Speaks- Uncovering Cardiac Intimal Sarcoma through Persistent Pleural Effusion

Introduction: Primary malignant cardiac tumors are extremely rare, with an incidence rate of less than 0.005%, and among these, intimal sarcoma is a poorly differentiated, highly aggressive tumor associated with a poor prognosis. Symptoms range from fever, weight loss, dyspnea, and orthopnea to embolic phenomena leading to stroke. Pleural effusion is an uncommon and underreported manifestation of this tumor. Case Presentation: A 67-year-old woman presented to the pulmonary clinic for a work-up of a left-sided pleural effusion with a 2-month history of exertional dyspnea, palpitations, and dry cough. The Holter monitor identified episodes of atrial fibrillation, and ECHO showed moderate to severe mitral stenosis and preserved ejection fraction of 59%. Thoracocentesis revealed lymphocytic effusion, negative cytology, and culture; other labs showed unremarkable immunological markers. A PET scan revealed a small left pleural effusion with minimal FDG uptake and nonspecific increased FDG uptake within the left atrial appendage. TEE revealed a large left atrial mass, which was initially thought to be a left atrial thrombus or myxoma. Cardiac MRI characterized the mass as hyperintense on T2-weighted sequences, enhancement on the first pass of gadolinium, and hyperintense on late gadolinium enhancement sequences, suggesting malignancy, as opposed to a thrombus. The patient had tumor excision, revealing a 7.5 cm Intimal-type sarcoma with non-eventful post-op recovery. Discussion: Intimal (spindle cell) sarcoma is an aggressive cardiac tumor that typically arises from large vessels and pulmonary veins, though it rarely involves the left atrium. Histologically, these tumors show positive immunoreactivity to vimentin, osteopontin, and Murine double minute 2[MDM2] with variable expression of other markers. While vascular markers like CD31 and CD34 are usually negative, they may sometimes show focal positivity. Immunohistochemistry is vital for diagnosis, with MDM2 overexpression seen in over 70% of cases. Among these tumors, about 40% of cases metastasize to the lungs, causing left-sided pleural effusion presenting with nonspecific symptoms such as dyspnea and orthopnea, often posing diagnostic challenges due to their rarity and similarity to non-neoplastic conditions, delaying diagnosis. Intimal sarcoma prognosis is poor, with average survival ranging from 3 months to 1 year, but early surgical intervention can improve outcomes.

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Journal
Circulation
Published
2025-11-03
DOI
https://doi.org/10.1161/circ.152.suppl_3.4366953
Primary Topic
Cardiac tumors and thrombi
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article
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Abstract 4366953: When the Pleural Effusion Speaks- Uncovering Cardiac Intimal Sarcoma through Persistent Pleural Effusion

Fnu Anamika, Akram Abushamma, Vinayak Hegde, Scott E. Kilpatrick et al.
Circulation
Cardiac tumors and thrombi
article

Abstract 4366953: When the Pleural Effusion Speaks- Uncovering Cardiac Intimal Sarcoma through Persistent Pleural Effusion

Fnu Anamika, Akram Abushamma, Vinayak Hegde, Scott E. Kilpatrick, Gabriel Sullivan, Sakshi Dixit, Mohammed Abdelaziz, Deeven Karki
article en

Abstract

Introduction: Primary malignant cardiac tumors are extremely rare, with an incidence rate of less than 0.005%, and among these, intimal sarcoma is a poorly differentiated, highly aggressive tumor associated with a poor prognosis. Symptoms range from fever, weight loss, dyspnea, and orthopnea to embolic phenomena leading to stroke. Pleural effusion is an uncommon and underreported manifestation of this tumor. Case Presentation: A 67-year-old woman presented to the pulmonary clinic for a work-up of a left-sided pleural effusion with a 2-month history of exertional dyspnea, palpitations, and dry cough. The Holter monitor identified episodes of atrial fibrillation, and ECHO showed moderate to severe mitral stenosis and preserved ejection fraction of 59%. Thoracocentesis revealed lymphocytic effusion, negative cytology, and culture; other labs showed unremarkable immunological markers. A PET scan revealed a small left pleural effusion with minimal FDG uptake and nonspecific increased FDG uptake within the left atrial appendage. TEE revealed a large left atrial mass, which was initially thought to be a left atrial thrombus or myxoma. Cardiac MRI characterized the mass as hyperintense on T2-weighted sequences, enhancement on the first pass of gadolinium, and hyperintense on late gadolinium enhancement sequences, suggesting malignancy, as opposed to a thrombus. The patient had tumor excision, revealing a 7.5 cm Intimal-type sarcoma with non-eventful post-op recovery. Discussion: Intimal (spindle cell) sarcoma is an aggressive cardiac tumor that typically arises from large vessels and pulmonary veins, though it rarely involves the left atrium. Histologically, these tumors show positive immunoreactivity to vimentin, osteopontin, and Murine double minute 2[MDM2] with variable expression of other markers. While vascular markers like CD31 and CD34 are usually negative, they may sometimes show focal positivity. Immunohistochemistry is vital for diagnosis, with MDM2 overexpression seen in over 70% of cases. Among these tumors, about 40% of cases metastasize to the lungs, causing left-sided pleural effusion presenting with nonspecific symptoms such as dyspnea and orthopnea, often posing diagnostic challenges due to their rarity and similarity to non-neoplastic conditions, delaying diagnosis. Intimal sarcoma prognosis is poor, with average survival ranging from 3 months to 1 year, but early surgical intervention can improve outcomes.

CirculationVol. 152(Suppl_3)
Cleveland Clinic (US), Cleveland Clinic Akron General (US)
Openalex Percentile: Top 50%
Cardiac tumors and thrombi
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