Uematsu M, Okada M, Ishii N, Watanabe N, Yasufuku M
Department of Surgery, Kobe University, School of Medicine, Japan.
Kyobu Geka. 1997 Apr;50(4):325-30.
A 73-year-old male was admitted to our hospital because of abnormal shadow in the lung field. The pathological report of the percutaneous needle lung biopsy specimen under the CT scan was suggested lymphoma (lymphomatoid granulomatosis suspected), and the right middle lobectomy was performed. Histological and immunohistochemical examinations of the operative specimen revealed B-cell type malignant lymphoma (diffuse pleomorphic lymphoma, large cell type, high grade lymphoma). Primary pulmonary malignant lymphoma is a rare disorder, and it is difficult utilized to distinguish between true malignant lymphoma and lymphomatoid granulomatosis, or pseudolymphoma. Anyway, the first choice of the treatment is surgical excision, because of its satisfactory prognosis.
一名73岁男性因肺野异常阴影入住我院。CT扫描引导下经皮肺穿刺活检标本的病理报告提示为淋巴瘤(疑似淋巴瘤样肉芽肿病),遂行右肺中叶切除术。手术标本的组织学和免疫组化检查显示为B细胞型恶性淋巴瘤(弥漫性多形性淋巴瘤,大细胞型,高级别淋巴瘤)。原发性肺恶性淋巴瘤是一种罕见疾病,很难区分真正的恶性淋巴瘤与淋巴瘤样肉芽肿病或假性淋巴瘤。无论如何,治疗的首选是手术切除,因其预后良好。