Nakayama Masahiro, Takahashi Kuniaki, Hori Mitsuo, Okumura Toshiyuki, Saito Mistuaki, Yamakawa Mitsunori, Tabuchi Keiji, Hara Akira
Department of Otolaryngology and Head and Neck Surgery, Ibaraki Prefectural Central Hospital and Cancer Center, 6528 Koibuchi, Kasama, Ibaraki, Japan.
Auris Nasus Larynx. 2010 Dec;37(6):750-3. doi: 10.1016/j.anl.2010.04.007. Epub 2010 Jun 15.
Langerhans cell sarcoma (LCS), a neoplastic proliferation of Langerhans cells with malignant cytologic features, is a very rare disease. We report the case of a 62-year-old male with LCS arising in a cervical lymph node. Histologic examination of a biopsy specimen of the lymph node demonstrated a proliferation of Langerhans cells with malignant cytologic features. Immunohistochemically, the tumor cells were positive for S-100 protein, CD1a, and Langerin (CD207). These histomorphological findings supported the diagnosis of LCS. The patient underwent radiotherapy. Neither local recurrence nor distant metastasis was observed at 45 months after radiotherapy. Characteristic immunohistochemical findings were helpful to identify LCS, and head and neck surgeons should be aware of this rare disease entity.
朗格汉斯细胞肉瘤(LCS)是一种具有恶性细胞学特征的朗格汉斯细胞的肿瘤性增殖,是一种非常罕见的疾病。我们报告一例62岁男性,其颈部淋巴结发生LCS。对淋巴结活检标本的组织学检查显示具有恶性细胞学特征的朗格汉斯细胞增殖。免疫组织化学检查显示,肿瘤细胞S-100蛋白、CD1a和朗格素(CD207)呈阳性。这些组织形态学发现支持LCS的诊断。该患者接受了放射治疗。放疗后45个月未观察到局部复发或远处转移。特征性免疫组织化学结果有助于识别LCS,头颈外科医生应了解这种罕见的疾病实体。