Case report: Anterior mediastinal mass in a patient with pleural effusion and dyspnea

• Published in: Frontiers in surgery 2023-05, Vol.10, p.1088642
• Main Authors: Gu, Lin, Xin, Gaojie, Qu, Yue, Wang, Kai, Jiang, Ke, Xing, Shijie, Huang, Ai
• Format: Article
• Language: English
• Subjects: anterior mediastinal mass; complete response; composite lymphoma; dyspnea; gene rearrangement; Surgery
• ISSN: 2296-875X; 2296-875X
• DOI: 10.3389/fsurg.2023.1088642

Compound lymphoma is an uncommon type of lymphoid malignancy, and those consisting of concurrent B- and T-cell tumors are relatively rare. 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 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. 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.