Key result
A 17-year-old male presented with right heart failure caused by a rare ALK-negative anaplastic large cell lymphoma mediastinal mass infiltrating the right heart.
Case Report (n=1)
Highlights a rare presentation of ALK-negative anaplastic large cell lymphoma as right heart failure due to a large mediastinal mass.
Large RV mass with severe TR detected by echo in adolescent right heart failure; leaves open etiology, prognosis, and management.
A 17-year-old male was admitted with progressive dyspnea on exertion, generalized edema, loss of appetite, and weight loss for 4 months. Clinical examination revealed features of right heart failure. Transthoracic echo showed a large hyperechoic sessile mass (6.5 cm × 5 cm) in the right ventricle, extending to the right ventricular outflow tract with mild pericardial effusion. Color Doppler across the tricuspid valve showed severe tricuspid regurgitation. Contrast-enhanced computed tomography scan thorax showed a large heterogeneously enhancing soft tissue density lesion with multiple hypodense nonenhancing areas involving the anterior, middle, and posterior mediastinum, predominantly on the right with encasement and infiltration of mediastinal vessels, right atrium, right ventricle, trachea, bronchi, and right lung. Ultrasound-guided tru-cut biopsy of the mass showed anaplastic lymphoma kinase (ALK)-negative anaplastic large-cell lymphoma. A rare case of ALK-negative, anaplastic large cell lymphoma mediastinal mass as right heart failure in a young adult is unique.
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Harikishore et al. (2025) conducted a case report in Anaplastic Lymphoma Kinase-negative Anaplastic Large Cell Lymphoma (n=1). A 17-year-old male presented with right heart failure caused by a rare ALK-negative anaplastic large cell lymphoma mediastinal mass infiltrating the right heart.
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