• Arch Iran Med · Sep 2021

    Case Reports

    Relapse of Lymphangioleiomyomatosis Five Years after Bilateral-Lung Transplantation.

    • Jalal Heshmatnia, Maryam Sadat Mirenayat, Mitrasadat Rezaei, Felix Bongomin, Mehrdad Bakhshayeshkaram, Payam Tabarsi, Kambiz Sheikhy, and Vida Mortezaee.
    • Chronic Respiratory Diseases Research Center, National Research Institute of Tuberculosis and Lung Diseases (NIRTLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran.
    • Arch Iran Med. 2021 Sep 1; 24 (9): 701-703.

    AbstractPulmonary lymphangioleiomyomatosis (LAM) is an uncommon disease principally affecting women during childbearing years and eventually leading to progressive respiratory failure. Lung transplantation is a viable option for patients with end-stage disease. LAM-related complications remain common, but recurrence of LAM following allograft transplantation is rare. We present a 25-year-old woman who presented with progressive dyspnea five years after bilateral lung transplantation for end-stage LAM. Histological examination of transbronchial lung biopsy sample confirmed recurrent LAM. We changed cyclosporine to sirolimus and she is currently being considered for re-transplantation.© 2021 The Author(s). This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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