Key result
En bloc resection of a rare glandular cardiac myxoma yields an uneventful 9-month recovery.
Why the study?
Glandular differentiation within cardiac myxomas is rare, occurring in approximately 3% of cases, and can complicate diagnosis by mimicking metastatic adenocarcinoma.
Case Report (n=1)
Cardiac myxomas can rarely exhibit glandular differentiation, which must be accurately diagnosed to avoid confusion with metastatic adenocarcinoma.
Emphasizes need for precise histopathology to distinguish glandular myxomas from adenocarcinoma; leaves open long-term outcomes in larger cohorts.
Cardiac myxoma, a benign heart tumor, is the most common primary tumor of the heart. Glandular differentiation within these tumors is rare, occurring in approximately 3% of all cardiac myxomas. Its presence can complicate the diagnostic process. A 43-year-old Saudi male was referred with a two-month history of progressively increasing shortness of breath. Cardiovascular examination demonstrated a soft first heart sound with a plopping sound in the mitral area and a mid-diastolic murmur. A transthoracic echocardiogram revealed a large mass attached to the interatrial septum. A diagnosis of cardiac myxoma was made, and the patient underwent en bloc resection of the mass. Microscopic evaluation of the resected mass showed a neoplastic lesion with two components: first, a typical myxoma consisting of stellate and spindle cells in a myxomatous/hemorrhagic background; second, a glandular component consisting of separate, fused, and cribriform acini embedded within the myxomatous component. The acini were lined by a single row of columnar epithelial cells with basal nuclei and apical mucin. Occasional goblet cells were also identified. The postoperative period was uneventful, and on his recent follow-up in the clinic (nine months after the surgery), the patient is doing well with no complications. Herein, we emphasize the importance of accurately diagnosing such an entity, as it can be easily confused for a metastatic adenocarcinoma, especially in patients with a history of malignancy.
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AlAhmadi et al. (2021) conducted a case report in Cardiac myxoma (n=1). En bloc resection was evaluated. En bloc resection of a cardiac myxoma with rare glandular differentiation in a 43-year-old male resulted in an uneventful recovery with 0 complications at 9 months.
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