Primary Hepatic Lymphoma After Lung Transplantation: A Report of 2 Cases |
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Authors: | Edoardo Maria Muttillo Tristan Dégot Matthieu Canuet Marianne Riou Benjamin Renaud-Picard Sandrine Hirschi Blandine Guffroy Romain Kessler Anne Olland Pierre-Emmanuel Falcoz Patrick Pessaux Emanuele Felli |
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Affiliation: | 1. Digestive and Endocrine Surgery, Nouvel Hopital Civil, University of Strasbourg, Strasbourg, France;2. IHU Strasbourg, Institute of Image-Guided Surgery, Strasbourg, France;3. IRCAD, Research Institute Against Digestive Cancer, Strasbourg, France;4. Department of Surgical Sciences, Sapienza University of Rome, Rome Italy;5. Division of Respiratology and Strasbourg Lung Transplant Program, Nouvel Hopital Civil, University of Strasbourg, Strasbourg, France;6. Division of Hematology, ICANS, University of Strasbourg, Strasbourg, France;7. Division of Thoracic Surgery and Strasbourg Lung Transplant Program, Nouvel Hopital Civil, University of Strasbourg, Strasbourg, France |
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Abstract: | BackgroundDiffuse large B-cell lymphoma (DLBCL) is the most common subtype of non–Hodgkin lymphoma in the posttransplant setting. Treatment is based on chemotherapy; surgery is still debated and should be performed in very select cases.MethodsWe observed 2 patients out of 300 who underwent lung transplantation in the Nouvel Hopital Civil between 2013 and 2019 with primary hepatic lymphoma. Chemotherapy with a rituximab-cyclophosphamide, hydroxydaunorubicin, vincristine, prednisone protocol was performed in all patients. Mycophenolate mofetil was interrupted before treatment, and everolimus was introduced after chemotherapy by associating tacrolimus withdrawal.ResultsOne patient showed complete remission; after 7 years, no recurrence has been noticed. The second is still undergoing chemotherapy with no signs of disease progression.ConclusionsDLBCL risk is higher in solid organ transplant recipients than in the general population. Primary hepatic lymphoma diagnosis is often difficult and based on histologic findings after initial clinical and radiological suspicion of primary or secondary liver neoplasia. Diagnosis is challenging because no clinical, radiological, or biological features exist. Biopsy is always indicated for histologic confirmation. Chemotherapy is the mainstay of therapy, but surgery may be indicated in very select patients. |
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