Abstract
We report the case of a renal transplant recipient with pulmonary and splenic mucormycosis whose demise was accelerated by a myocardial abscess. Once pulmonary and splenic mucormycosis was diagnosed, liposomal amphotericin B was started and immunosuppressant treatments were discontinued. The pulmonary cavities regressed during treatment, but new myocardial and peri-allograft abscesses developed. The myocardial abscess diffusely infiltrated the left ventricular wall and was associated with akinesia, which led to sudden cardiac arrest. This case demonstrates a rare manifestation of mucormycosis and highlights the fatality and invasiveness of this infection.
| Original language | English |
|---|---|
| Pages (from-to) | 890-896 |
| Number of pages | 7 |
| Journal | Transplant Infectious Disease |
| Volume | 17 |
| Issue number | 6 |
| DOIs | |
| State | Published - 1 Dec 2015 |
Bibliographical note
Publisher Copyright:© 2015 Wiley Periodicals, Inc.
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Mucormycosis
- Myocardial abscess
- Renal transplantation
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