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      Is Open Access

      Primary thymic mucosa-associated lymphoid tissue lymphoma complicated with renal amyloidosis : A first case report

      case-report
      , MS a , , MS a , , MD, PhD b , , MS a , , MD, PhD a , , MD, PhD a , , MD, PhD a ,
      Medicine
      Wolters Kluwer Health
      MALT lymphoma, monoclonal immunoglobulinemia, renal amyloidosis, thymus

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          Abstract

          Introduction:

          Primary mucosa-associated lymphoid tissue (MALT) lymphomas originating in thymus is rare. And, there have been few reports of patients with MALT coexisting with amyloidosis. As far as we know, this was the first case report on MALT lymphoma associated with renal amyloidosis.

          Patient concerns:

          A 57-year-old man presented with nephrotic syndrome. Further workup revealed IgM-Lambda type monoclonal gammopathy. Bone marrow biopsy showed 8% clonal plasma cells. Renal biopsy confirmed the diagnosis of Lambda light chain AL amyloidosis. positron emission tomography/computed tomography showed thymic lesions which upon biopsy were diagnosed as MALT lymphoma of the thymus.

          Diagnosis:

          Primary thymic MALT lymphoma complicated with renal amyloidosis.

          Interventions:

          The patient underwent surgical resection of the thymus mass and 2 courses of chemotherapy.

          Outcomes:

          Follow-up data showed that the patient survived 18 months after surgical excision and chemotherapy.

          Conclusion:

          The case highlights the importance of screening for malignancy in patients with renal amyloidosis.

          Related collections

          Most cited references15

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          • Abstract: found
          • Article: not found

          Malignant lymphoma of mucosa-associated lymphoid tissue. A distinctive type of B-cell lymphoma.

          As illustrated in the two cases described in this paper close morphologic and immunohistochemical similarities exist between Mediterranean lymphoma (MTL) and primary gastrointestinal lymphoma of follicle center cell (FCC) origin as it occurs in Western countries. Similarities between the two conditions include a dense noninvasive monotypic lamina propria plasma cell infiltrate, present in all cases of MTL and in some cases of Western gastrointestinal FCC lymphoma, and an invasive infiltrate of FCCs morphologically distinct from the plasma cells. A distinctive lesion produced by individual gland invasion characterizes both types of lymphoma. A clonal relationship between the lamina propria plasma cells and the invasive FCCs, long suspected but never proved in MTL, can be demonstrated in Western cases. Many of the histologic and clinical features common to these lymphomas can be explained in the context of the normal maturation sequences of gut associated lymphoid tissue. It is suggested that MTL and Western cases of primary FCC gastrointestinal lymphoma share a common histogenesis from mucosa associated lymphoid tissue.
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            • Record: found
            • Abstract: found
            • Article: not found

            Kidney diseases associated with monoclonal immunoglobulin M-secreting B-cell lymphoproliferative disorders: a case series of 35 patients.

            Kidney diseases associated with immunoglobulin M (IgM) monoclonal gammopathy are poorly described, with few data for patient outcomes and renal response.
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              • Record: found
              • Abstract: found
              • Article: not found

              Kidney Involvement of Patients with Waldenström Macroglobulinemia and Other IgM-Producing B Cell Lymphoproliferative Disorders.

              Kidney involvement in Waldenström macroglobulinemia is less well described compared with kidney manifestations in multiple myeloma.
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                Author and article information

                Journal
                Medicine (Baltimore)
                Medicine (Baltimore)
                MEDI
                Medicine
                Wolters Kluwer Health
                0025-7974
                1536-5964
                27 March 2020
                March 2020
                : 99
                : 13
                : e19462
                Affiliations
                [a ]Department of Nephrology and Institute of Nephrology, Sichuan Academy of Medical Science and Sichuan Provincial People's Hospital, Chengdu, China
                [b ]Division of Nephrology and Hypertension, Mayo Clinic, Rochester, Minnesota, USA.
                Author notes
                []Correspondence: Wei Wang, Department of Nephrology and Institute of Nephrology, Sichuan Academy of Medical Science and Sichuan Provincial People's Hospital, Chengdu, 610072, China (e-mail: wangweisz@ 123456med.uestc.edu.cn ).
                Article
                MD-D-19-05678 19462
                10.1097/MD.0000000000019462
                7220216
                32221068
                acc55ca7-2839-49ef-9636-455e661afbf5
                Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc.

                This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0

                History
                : 25 July 2019
                : 23 December 2019
                : 6 February 2020
                Categories
                5200
                Research Article
                Clinical Case Report
                Custom metadata
                TRUE

                malt lymphoma,monoclonal immunoglobulinemia,renal amyloidosis,thymus

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