Gao Shengnan, Xing Bin, Lichao Sun, Luo Jie, Tang Jiao, Wang Ye, Zhang Xiaoyan
Department of Clinical Laboratory, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, National Cancer Center/National Clinical Research Center for Cancer/State Key Laboratory of Molecular Oncology, Beijing, China.
Department of Pulmonary and Critical Care Medicine, Center of Respiratory Medicine, China-Japan Friendship Hospital, Beijing, China.
Front Oncol. 2022 Sep 20;12:895924. doi: 10.3389/fonc.2022.895924. eCollection 2022.
Granulosa cell tumor (GCT) is a rare tumor that originates from neural/Schwann cells. GCTs can occur at any age and at any site in the body. The most common site is the tongue, followed by the mammary gland, upper respiratory tract ( throat and bronchus), and gastrointestinal tract (esophagus, large intestine and perianal area, stomach, small intestine, and bile duct). Malignant GCTs account for less than 1%-2% of all GCTs. Fewer than five GCTs in the thoracic wall have been reported, almost all of these benign. Here, we report a new case of malignant GCT of the thoracic wall, with rib invasion and pleural metastasis, in an Asian male. Microscopic examination revealed round, granular cells with eosinophilic cytoplasm and without prominent atypia. Despite these findings the disease showed rapid clinical progression. In summary, the tumor, although histologically 'benign', was clinically 'malignant'.
颗粒细胞瘤(GCT)是一种起源于神经/施万细胞的罕见肿瘤。GCT可发生于任何年龄和身体的任何部位。最常见的部位是舌头,其次是乳腺、上呼吸道(咽喉和支气管)以及胃肠道(食管、大肠和肛周区域、胃、小肠和胆管)。恶性GCT占所有GCT的比例不到1%-2%。据报道,胸壁的GCT病例少于5例,几乎所有这些病例都是良性的。在此,我们报告一例亚洲男性胸壁恶性GCT的新病例,该病例伴有肋骨侵犯和胸膜转移。显微镜检查显示为圆形、颗粒状细胞,细胞质嗜酸性,无明显异型性。尽管有这些发现,但该疾病临床进展迅速。总之,该肿瘤虽然组织学上为“良性”,但临床上为“恶性”。