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Mayo Clinic Proceedings: Innovations, Quality & Outcomes
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    • Case report
      Open Access

      Pulmonary Vascular Disease Due to Plasma Cell Dyscrasia

      Mayo Clinic Proceedings: Innovations, Quality & Outcomes
      Vol. 5Issue 1p210–218Published online: November 20, 2020
      • Indranee Rajapreyar
      • Joanna Joly
      • Jose Tallaj
      • Salpy V. Pamboukian
      • Ayman Haj Assad
      • Carrie Lenneman
      • and others
      Cited in Scopus: 0
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        Pulmonary hypertension (PH) has been described in myeloproliferative disorders; monoclonal plasma cell disorder such as polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes syndrome; and plasma cell dyscrasias such as multiple myeloma and amyloidosis. We describe 4 cases of PH likely due to pulmonary vascular involvement and myocardial deposition from light chain deposition disease, amyloidosis, and multiple myeloma. On the basis of our clinical experience and literature review, we propose screening for plasma cell dyscrasia in patients with heart failure with preserved ejection fraction, unexplained PH, and hematological abnormalities.
        Pulmonary Vascular Disease Due to Plasma Cell Dyscrasia
      • Case report
        Open Access

        Cell-Based Therapy for Myocardial Dysfunction After Fontan Operation in Hypoplastic Left Heart Syndrome

        Mayo Clinic Proceedings: Innovations, Quality & Outcomes
        Vol. 1Issue 2p185–191Published online: August 2, 2017
        • Muhammad Y. Qureshi
        • Allison K. Cabalka
        • Shakila P. Khan
        • Donald J. Hagler
        • Dawit T. Haile
        • Bryan C. Cannon
        • and others
        Cited in Scopus: 0
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          Myocardial dysfunction after Fontan palliation for univentricular congenital heart disease is a challenging clinical problem. The medical treatment has a limited impact, with cardiac transplant being the ultimate management step. Cell-based therapies are evolving as a new treatment for heart failure. Phase 1 clinical trials using regenerative therapeutic strategies in congenital heart disease are ongoing. We report the first case of autologous bone marrow–derived mononuclear cell administration for ventricular dysfunction, 23 years after Fontan operation in a patient with hypoplastic left heart syndrome.
        Page 1 of 1
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