树突状细胞间质瘤:罕见病例报告及文献综述

Kumudavalli Muthukumarappan, Maya Menon
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引用次数: 0

摘要

交织树突状细胞瘤/肉瘤(IDCS)是一种极为罕见的侵袭性肿瘤,预后极差。IDCS产生于抗原递呈细胞,累及结节和结节外部位。本研究旨在评估一例 IDCS 病例及其诊断难题。患者为 21 岁女性,无合并症,骨髓穿刺和活检以及淋巴结切除活检均显示非典型单核浸润,S100-diffuse、CD68、LCA 和 Ki67 免疫组化阳性。在此,我们报告了一例淋巴结肿瘤和骨髓浸润的 IDCS 病例。IDCS是一种行为不确定的侵袭性疾病,需要高度怀疑才能确诊。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Interdigitating Dendritic Cell Tumour: A Rare Case Report with Review of Literature
Interdigitating dendritic cell tumour/sarcoma (IDCS) is an exceedingly uncommon and aggressive tumour with a dismal prognosis. IDCS arises from antigen-presenting cells, which involve nodal and extranodal sites. The aim of the study is to evaluate a case of IDCS and its diagnostic challenges. A 21-year-old female with no comorbidities, a bone marrow aspirate and biopsy and an excision biopsy of the lymph node shows atypical mononuclear infiltrates that were immunohistochemically positive for S100-diffuse, CD68, LCA and Ki67. Here, we report a single case of IDCS with a tumour arising from the lymph node and bone marrow infiltration. IDCS is an aggressive disease with uncertain behaviour; strong suspicion is required to establish a diagnosis.
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