Zhao Gang, Luo Meng, Wu Zhi-Yong, Liu Qiang, Zhang Bin, Gao Run-Ling, Zhang Zhi-Qi
Department of General Surgery, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Int J Surg Pathol. 2009 Aug;17(4):347-53. doi: 10.1177/1066896908324128. Epub 2008 Sep 19.
Langerhans cell sarcoma (LCS) is a rare proliferation of Langerhans cells with overtly malignant cytologic features and spreads aggressively. LCSs show a multiorgan involvement, including skin, lymph nodes, lung, and bone. The authors report an LCS in a 74-year-old woman that involved the gallbladder and the peritoneal lymph nodes. Imaging revealed a tumor in the gallbladder and the peritoneal lymph nodes. The tumor cells were positive for CD1a, S-100 protein, and Langerin (CD207). Although the ultrastructural analysis failed to demonstrate any Birbeck granules, the histomorphological and immunohistochemical findings supported the diagnosis of LCS. After surgical resection, she showed no recurrent or metastatic signs for 8 months without any other adjuvant therapy. This is the first case of LCS involving the gallbladder and the peritoneal lymph nodes. This report also includes a review of the literature concerning this rare disease.
朗格汉斯细胞肉瘤(LCS)是一种罕见的朗格汉斯细胞增殖性疾病,具有明显的恶性细胞学特征且侵袭性生长。LCS可累及多器官,包括皮肤、淋巴结、肺和骨。作者报告了一例74岁女性的LCS,病变累及胆囊和腹膜后淋巴结。影像学检查发现胆囊和腹膜后淋巴结有肿瘤。肿瘤细胞CD1a、S-100蛋白和朗格素(CD207)呈阳性。尽管超微结构分析未发现任何伯贝克颗粒,但组织形态学和免疫组化结果支持LCS的诊断。手术切除后,未经任何其他辅助治疗,她在8个月内未出现复发或转移迹象。这是首例累及胆囊和腹膜后淋巴结的LCS。本报告还包括了关于这种罕见疾病的文献综述。