Watanabe Hironosuke, Yamasaki Naoya, Miyazaki Takuro, Matsumoto Keitaro, Tsuchiya Tomoshi, Abe Kuniko, Nagayasu Takeshi
Division of Surgical Oncology, Department of Surgery, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan.
Department of Pathology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Surg Case Rep. 2019 Jul 24;5(1):118. doi: 10.1186/s40792-019-0674-x.
Inflammatory myofibroblastic tumor (IMT) of the lung is rare. This disease often shows neoplastic features with anaplastic lymphoma kinase positiveness as well as inflammatory features, such as steroid-responsive immunoglobulin G4 (IgG4)-related sclerosing disease. Since many cases have been reported as advanced, various treatment strategies should be considered based on clinical and biological features of each case.
We report a 49-year-old male with IMT, which seemed invading the left atrium from preoperative imaging modalities. Serological and pathological examinations from the biopsy specimen revealed high expression of anaplastic lymphoma kinase expression in the tumor. On the other hand, IgG4/IgG ration in the tumor was small, where a therapeutic effect of steroid was not expected, leading to surgical treatment rather than a steroid administration. The tumor was completely resected en bloc with the right lower lobe of the lung and a part of the left atrium. The postoperative course of the patient was uneventful. The patient has remained recurrence free over 5 years from the surgery.
In this case, preoperative biological assessment prior to the treatment led to a good clinical course. We believe that molecular biological examination is important in the determination of treatment strategy for this rare disease as well as imaging modalities.
肺炎性肌纤维母细胞瘤(IMT)较为罕见。该疾病常表现出具有间变性淋巴瘤激酶阳性的肿瘤特征以及炎性特征,如类固醇反应性免疫球蛋白G4(IgG4)相关硬化性疾病。由于许多病例报告为晚期,应根据每个病例的临床和生物学特征考虑各种治疗策略。
我们报告一名49岁患有IMT的男性,术前影像学检查显示肿瘤似乎侵犯了左心房。活检标本的血清学和病理学检查显示肿瘤中间变性淋巴瘤激酶表达高。另一方面,肿瘤中IgG4/IgG比值较小,预计类固醇治疗无效,因此采取手术治疗而非给予类固醇。肿瘤与右下肺叶及部分左心房整块完整切除。患者术后恢复顺利。自手术以来,患者已5年无复发。
在本病例中,治疗前的术前生物学评估带来了良好的临床病程。我们认为分子生物学检查对于确定这种罕见疾病的治疗策略以及影像学检查同样重要。