交叉指状树突状细胞肉瘤单独发生于腋窝。

Journal of the Korean Surgical Society Pub Date : 2012-05-01 Epub Date: 2012-04-26 DOI:10.4174/jkss.2012.82.5.330
Sun Wook Han, Zi Sun Kim, Hyuk Moon Kim, Jihyoun Lee, Gil Ho Kang, Hyun Deuk Cho, Sung Yong Kim, Nae Kyeong Park, Cheol Wan Lim, Min Hyk Lee
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引用次数: 34

摘要

间指树突状细胞肉瘤(IDCS)是一种非常罕见的疾病,其预后已知是侵袭性的。本文报告一例在顺天乡大学医院诊断为腋窝区IDCS的病例。一位57岁的女性因左腋窝肿块来到顺天乡大学医院。这团东西又硬又固定。计算机断层扫描发现左侧腋窝有7厘米淋巴结,核心活检怀疑为肉瘤。在另一项研究中,除了腋窝病变外,没有特别的发现。左腋窝淋巴结清扫(ⅰ、ⅱ级),病理报告最终显示IDCS。患者仅行放射治疗,随访13个月,无复发。IDCS是一种非常罕见的肉瘤,难以诊断且进展迅速。因此,治疗非常困难。经过更多的经验,才能更好地建立正确的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Interdigitating dendritic cell sarcoma occured alone in axilla.

Interdigitating dendritic cell sarcoma (IDCS) is a very rare disease around the world and its prognosis is known to be aggressive. This reports a case diagnosed as IDCS of the axillary region treated in Soonchunhyang University Hospital. A 57-year-old female visited Soonchunhyang University Hospital with a left axillary mass. The mass was hard and fixed. Computed tomography observed a 7 cm lymph node at the left axilla, and core biopsy suspected sarcoma. In another study, there was no specific finding except the axillary lesion. Left axillary lymph node dissection (level I, II) was conducted and the pathologic report finally showed IDCS. The patient was treated with only radiotherapy and followed up without recurrence for 13 months up to now. IDCS is a very rare sarcoma that is hard to diagnose and progresses fast. Thus, treatment is very difficult. Proper treatment can be better established after more experiences.

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