Dan L V, Huang Yunfeng, Yang Hui, Liu Shixi, Wang Haiyang, Wang Min
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2014 Apr;28(8):522-6.
To investigate the clinical manifestation, pathological characteristics, treatment and prognosis of dendritic cell tumor.
Four cases of nasal and pharyngeal dendritic cell tumor were described, including two cases of follicular dendritic cell sarcoma (FDCS), one case of Langerhans cell histiocytosis (LCH) and one case of Langer hans cell sarcoma (LCS). One of the patients with FDCS received multimodality therapy (surgery combined with chemotherapy), and the other patient only received chemotherapy and radiotherapy. The patients with LCH or LSC were treated by surgery.
Of the two FDCS patients, one achieved complete remission after treatment by surgery combined with four cycles of CHOP chemotherapy regimen and concurrent radiotherapy (50 Gy), and the other who only received chemotherapy and radiotherapy survived with tumor for more than seven months of follow up. The patient of LCH was followed up for more than 2 years after surgery without recurrence or metastasis. The patient of LCS did not undergo radiotherapy or chemotherapy after surgery and died after 10 months of follow up.
Dendritic cell tumor is a group of very rare tumor and can be easily misdiagnosed in clinic, the confirmed diagnosis of which relies on histopathological features, immunohistochemistry combined with electron microscopy. FDCS, LCH and LCS have different pathological features, immunophenotypes and prognosis.
探讨树突状细胞瘤的临床表现、病理特征、治疗及预后。
描述4例鼻咽喉树突状细胞瘤,其中包括2例滤泡性树突状细胞肉瘤(FDCS)、1例朗格汉斯细胞组织细胞增多症(LCH)和1例朗格汉斯细胞肉瘤(LCS)。1例FDCS患者接受了多模式治疗(手术联合化疗),另1例仅接受化疗和放疗。LCH或LCS患者接受手术治疗。
2例FDCS患者中,1例在接受手术联合4周期CHOP化疗方案及同步放疗(50 Gy)后达到完全缓解,另1例仅接受化疗和放疗,随访7个多月时肿瘤仍存活。LCH患者术后随访2年多无复发或转移。LCS患者术后未接受放疗或化疗,随访10个月后死亡。
树突状细胞瘤是一组非常罕见的肿瘤,临床易误诊,确诊依赖组织病理学特征、免疫组化结合电子显微镜检查。FDCS、LCH和LCS具有不同的病理特征、免疫表型及预后。