Myeloid sarcoma of the heart-A clinicopathological correlation

Kristijan Skok1, Martin Zacharias1, Nicolas Verheyen2

  • 1Diagnostic and Research Institute of Pathology, Medical University of Graz, Stiftingtalstraße 6, 8010, Graz, Austria.

PubMed

Insights

A rare case of cardiac myeloid sarcoma is presented in a patient with acute myeloid leukemia and a history of stem cell transplantation. This infiltrative cardiomyopathy led to fatal heart failure.

Area of Science:

  • Cardiology
  • Hematology
  • Oncology

Background:

  • Cardiac involvement in acute myeloid leukemia (AML) is uncommon.
  • Myeloid sarcoma, an extramedullary tumor of myeloid blasts, can rarely infiltrate the heart.
  • Infiltrative cardiomyopathy can present as heart failure with preserved ejection fraction.

Purpose of the Study:

  • To report a rare case of primary cardiac myeloid sarcoma.
  • To highlight the diagnostic challenges and clinical presentation of cardiac myeloid sarcoma.
  • To discuss the implications for patients with a history of AML and stem cell transplantation.

Main Methods:

  • Case report presentation.
  • Review of patient history, clinical presentation, and diagnostic findings.
  • Echocardiography and autopsy findings are detailed.

Main Results:

  • A 63-year-old woman with AML and stem cell transplant history presented with acute heart failure.
  • Echocardiography showed severe ventricular hypertrophy and elevated filling pressures, suggestive of infiltrative cardiomyopathy.
  • Autopsy revealed an enlarged heart with a characteristic fish-flesh appearance, confirming cardiac myeloid sarcoma.

Conclusions:

  • Cardiac myeloid sarcoma is a rare but critical complication in AML patients.
  • Early recognition and diagnosis are crucial for management, though prognosis remains poor.
  • This case underscores the importance of considering extramedullary myeloid disease in the heart.