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Case report: Anterior mediastinal mass in a patient with pleural effusion and dyspnea
BACKGROUND: Compound lymphoma is an uncommon type of lymphoid malignancy, and those consisting of concurrent B- and T-cell tumors are relatively rare. CASE SUMMARY: A 41-year-old man was presented with a 1-month history of progressively worsening cough, chest tightness, and dyspnea after exercise, w...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10189153/ https://www.ncbi.nlm.nih.gov/pubmed/37206341 http://dx.doi.org/10.3389/fsurg.2023.1088642 |
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author | Gu, Lin Xin, Gaojie Qu, Yue Wang, Kai Jiang, Ke Xing, Shijie Huang, Ai |
author_facet | Gu, Lin Xin, Gaojie Qu, Yue Wang, Kai Jiang, Ke Xing, Shijie Huang, Ai |
author_sort | Gu, Lin |
collection | PubMed |
description | BACKGROUND: Compound lymphoma is an uncommon type of lymphoid malignancy, and those consisting of concurrent B- and T-cell tumors are relatively rare. CASE SUMMARY: A 41-year-old man was presented with a 1-month history of progressively worsening cough, chest tightness, and dyspnea after exercise, which could be relieved following rest. Contrast-enhanced computed tomography scan demonstrated a 7.4 × 4.9 cm(2) heterogeneous mass in the anterior mediastinum, where a large area of cystic liquid existed, and multiple enlarged lymph nodes in the mediastinum. Since the biopsy failed to yield an exact diagnosis and there was no sign of metastasis, the tumor was surgically resectioned. Surgical findings included obscure boundaries and consistent tumor stiffness with pericardial and pleural invasion. Further pathological examination combined with immunophenotype and gene rearrangement test found the mass composite of angioimmunoblastic T-cell lymphoma (AITL) and B-cell lymphoma. The patient recovered well after R0 resection and received chemotherapy with four cycles of CHOP combined with chidamide 2 weeks after surgery. The patient has had a complete response for over 60 months. CONCLUSION: In conclusion, we reported a composite lymphoma of AITL combined with B-cell lymphomas. Our experience provides the first successful attempt to treat this rare disease with combined surgery and chemotherapy. |
format | Online Article Text |
id | pubmed-10189153 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101891532023-05-18 Case report: Anterior mediastinal mass in a patient with pleural effusion and dyspnea Gu, Lin Xin, Gaojie Qu, Yue Wang, Kai Jiang, Ke Xing, Shijie Huang, Ai Front Surg Surgery BACKGROUND: Compound lymphoma is an uncommon type of lymphoid malignancy, and those consisting of concurrent B- and T-cell tumors are relatively rare. CASE SUMMARY: A 41-year-old man was presented with a 1-month history of progressively worsening cough, chest tightness, and dyspnea after exercise, which could be relieved following rest. Contrast-enhanced computed tomography scan demonstrated a 7.4 × 4.9 cm(2) heterogeneous mass in the anterior mediastinum, where a large area of cystic liquid existed, and multiple enlarged lymph nodes in the mediastinum. Since the biopsy failed to yield an exact diagnosis and there was no sign of metastasis, the tumor was surgically resectioned. Surgical findings included obscure boundaries and consistent tumor stiffness with pericardial and pleural invasion. Further pathological examination combined with immunophenotype and gene rearrangement test found the mass composite of angioimmunoblastic T-cell lymphoma (AITL) and B-cell lymphoma. The patient recovered well after R0 resection and received chemotherapy with four cycles of CHOP combined with chidamide 2 weeks after surgery. The patient has had a complete response for over 60 months. CONCLUSION: In conclusion, we reported a composite lymphoma of AITL combined with B-cell lymphomas. Our experience provides the first successful attempt to treat this rare disease with combined surgery and chemotherapy. Frontiers Media S.A. 2023-05-03 /pmc/articles/PMC10189153/ /pubmed/37206341 http://dx.doi.org/10.3389/fsurg.2023.1088642 Text en © 2023 Gu, Xin, Qu, Wang, Jiang, Xing and Huang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Surgery Gu, Lin Xin, Gaojie Qu, Yue Wang, Kai Jiang, Ke Xing, Shijie Huang, Ai Case report: Anterior mediastinal mass in a patient with pleural effusion and dyspnea |
title | Case report: Anterior mediastinal mass in a patient with pleural effusion and dyspnea |
title_full | Case report: Anterior mediastinal mass in a patient with pleural effusion and dyspnea |
title_fullStr | Case report: Anterior mediastinal mass in a patient with pleural effusion and dyspnea |
title_full_unstemmed | Case report: Anterior mediastinal mass in a patient with pleural effusion and dyspnea |
title_short | Case report: Anterior mediastinal mass in a patient with pleural effusion and dyspnea |
title_sort | case report: anterior mediastinal mass in a patient with pleural effusion and dyspnea |
topic | Surgery |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10189153/ https://www.ncbi.nlm.nih.gov/pubmed/37206341 http://dx.doi.org/10.3389/fsurg.2023.1088642 |
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