Yoshikawa T, Noguchi Y, Matsukawa H, Kondo J, Matsumoto A, Nakatani Y, Kitamura H, Ito T
First Department of Surgery, Yokohama City University, School of Medicine, Japan.
Surg Today. 1994;24(6):544-7. doi: 10.1007/BF01884576.
We report herein the rare case of a thymus carcinoid producing parathyroid hormone (PTH)-related protein (PTHrP) found in a 43-year-old Japanese man who presented with a 19-month history of dyspnea. The diagnosis of a carcinoid was established by light microscopic, electron microscopic, and immunohistochemical examinations. The tumor was considered to be thymic in origin because of its anatomic location, the presence of feeders to the tumor (derived from the internal thoracic arteries), and the fact that no other tumors from which it could have originated were found. After an excisional biopsy, which revealed PTH-related immunoreactivity in the tumor cells, 60 Gy of irradiation was delivered, resulting in a 48% reduction in the size of the tumor. Flow cytometry showed a diploid DNA pattern, with 94% of the cells in the G1 phase, 4% in the S phase, 2% in the G2 + M phase, and a G2 + M/G1 ratio of 1.95. The primary cell culture showed some cells adopted in a cord-like pattern. To our knowledge, this is the first report of a carcinoid tumor in which positive staining for PTHrP by immunohistochemical methods was demonstrated.
我们在此报告一例罕见病例,一名43岁日本男性患者,出现19个月的呼吸困难症状,其胸腺类癌产生甲状旁腺激素(PTH)相关蛋白(PTHrP)。通过光学显微镜、电子显微镜及免疫组织化学检查确诊为类癌。鉴于肿瘤的解剖位置、肿瘤供血血管(源自胸廓内动脉)以及未发现其他可能的原发肿瘤部位,该肿瘤被认为起源于胸腺。切除活检显示肿瘤细胞存在PTH相关免疫反应性后,给予60 Gy放疗,肿瘤大小缩小48%。流式细胞术显示DNA为二倍体模式,94%的细胞处于G1期,4%处于S期,2%处于G2 + M期,G2 + M/G1比值为1.95。原代细胞培养显示部分细胞呈条索状排列。据我们所知,这是首例经免疫组织化学方法证实PTHrP阳性染色的类癌肿瘤报告。