AI Article Synopsis

  • Hodgkin lymphoma (HL) is a common lymphatic system cancer with cure rates of 80-85%, but treatment can lead to significant heart issues, particularly from anthracycline drugs.
  • A 60-year-old man with stage IIIB HL experienced sudden cardiogenic shock after starting chemotherapy, although he eventually recovered cardiac function after medical support.
  • This case underscores the unpredictability of cardiotoxicity in HL treatments and suggests potential genetic factors contributing to an individual's risk, highlighting the need for better understanding in this area.

Article Abstract

Introduction: Hodgkin lymphoma (HL) is one of the most common types of cancers of the lymphatic system. The currently available therapies enable a cure in approximately 80-85% of treated patients. However, the cardiotoxicity of HL treatment has become a major cause of morbidity and mortality in survivors mainly related to the use of anthracycline.

Case Report: An HL, staged IIIB, was diagnosed in a 60-year-old man with no cardiovascular disease. During the first cycle of ABVD chemotherapy (Adriamycin; bleomycin; vinblastine; dacarbazine), near the end of the dacarbazine infusion, the patient presented a sudden cardiogenic shock characterized by a severe left ventricular systolic dysfunction. Laboratory and instrumental examinations performed did not suggest any specific etiology. After 15 days of medical support, the patient presented a complete cardiac function and clinical recovery. Subsequently bendamustine chemotherapy was started because of its limited extrahematological toxicity, but after 4 cycles the patient had progressive disease and died of septic shock. We concluded that a very rare hyperacute anthracycline cardiotoxicity was the most likely reason for this critical scenario.

Conclusions: This rare event stresses our inability to correctly predict the risk of a patient developing cardiotoxicity and also highlights the need to improve the knowledge of underlying pathophysiological mechanisms; in fact, it suggests a possible genetic predisposition to develop cardiotoxicity due to a relatively limited dosage.

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Source
http://dx.doi.org/10.1159/000480291DOI Listing

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