Key result
A rare case of disseminated ALK-positive anaplastic large cell lymphoma in a 26-year-old woman demonstrated extensive cardiac and thymic infiltration, culminating in fatal pulmonary thromboembolism.
Why the study?
Cardiac lymphoma is rare, and widespread cardiac and thymic infiltration by systemic ALK-positive anaplastic large cell lymphoma had not been documented.
Case Report (n=1)
No
This report documents a rare case of widespread cardiac and thymic infiltration by systemic ALK-positive anaplastic large cell lymphoma.
Cardiac lymphoma is a rare entity. In this setting, the secondary involvement of the heart is far more frequent than the primary cardiac lymphoma. Herein, we present an autopsy case of a disseminated anaplastic lymphoma kinase (ALK)-positive anaplastic large cell lymphoma with a dominant mediastinal involvement. Extensive cardiac infiltration with the near replacement of the myocardial wall by the neoplastic cells was observed. A total of nine isolated case reports of anaplastic large cell lymphoma with cardiac involvement were found in the English-language literature, and a widespread cardiac and thymic infiltration by the systemic ALK-positive anaplastic large cell lymphoma has not been documented. An incidental regenerative nodule was also identified in the liver. The patient died of pulmonary thromboembolism and cardiac arrest.
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Nambiyar et al. (2020) conducted a case report in ALK+ Anaplastic large cell lymphoma (n=1). Disseminated ALK-positive anaplastic large cell lymphoma was evaluated on Clinical outcome and autopsy findings. A rare case of disseminated ALK-positive anaplastic large cell lymphoma in a 26-year-old woman demonstrated extensive cardiac and thymic infiltration, culminating in fatal pulmonary thromboembolism.
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