青年脊柱郎格汉斯细胞组织细胞增多症的细胞组织学相关性

S. Asotra, Sudarshan K. Sharma, S. Thakur
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引用次数: 0

摘要

郎格罕细胞组织细胞增多症(LCH)是一种罕见的多系统疾病,常见的组织病理学发现为郎格罕型细胞增殖与炎症细胞环境混合。骨骼受累是儿童和年轻人常见的表现。最近使用细胞特异性基因表达谱的研究表明,LCH来源于骨髓来源的未成熟髓系树突状细胞。我们报告了一例年轻人的颈椎孤立性LCH,经细针抽吸诊断为肩部疼痛和麻木,并经组织病理学和免疫组织化学证实。对其进行了肿瘤切除和脊椎稳定治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cytohistological correlation of Langerhans cell histiocytosis of the spine in a young adult
Langerhans cell histiocytosis (LCH) is a rare multisystem disorder with a common histopathological finding of Langerhans-type cell proliferation mixed with a milieu of inflammatory cells. Bone involvement is a common presentation occurring in children and young adults. Recent studies using cell-specific gene expression profiling suggest that LCH arises from bone marrow-derived immature myeloid dendritic cells. We present a case of solitary LCH of cervical vertebrae in a young adult with pain and numbness in the shoulder diagnosed on fine-needle aspiration and confirmed on histopathology and immunohistochemistry. It was treated with tumor resection and stabilization of the vertebrae.
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