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部单心卡斯特曼病的转变为状状细胞肉瘤

Yingying Li¹, Yue Shao², Xiumei Sun³

¹Department of Otolaryngology-Head and Neck Surgery, Yantai Affiliated Hospital of Binzhou Medical University, Yantai, China.

The Laryngoscope

|June 19, 2024

概括

单心卡斯特勒曼的恶性转变.

科学领域:

在瘤学瘤学.
头部和部手术头部和部手术
病理学病理学病理学

背景情况:

单心卡斯特曼病 (UCD) 是一种罕见的淋巴增殖性疾病.
胰腺癌的恶性转变非常罕见,特别是在头部和部区域.

研究的目的:

报告一个极为罕见的UCD恶性转变为FDCS的头部和部病例.
为了突出诊断挑战和管理这个罕见的实体.

主要方法:

患者呈现出一个大部质量.
诊断工作包括成像,血液检测,血清学评估,切口活检,组织病理学和免疫组织化学.
对UCD的淋巴切除术患者之前病史的审查.

主要成果:

组织病理学检查证实了FDCS,与之前的UCD的恶性转变一致.
这位患者有UCD病史,8年前被诊断为UCD.
这代表了一种罕见的UCD恶性转变在头部和部的例子.

结论:

在头部和部,UCD恶性转化为FDCS非常罕见.
早期诊断和适当的治疗,包括区域淋巴结切除,至关重要.
定期的随访对于最佳的患者结果至关重要.

关键词:

毛囊状树突细胞肉瘤毛囊状树突细胞肉瘤恶性转变的恶性转变子子子子手术手术手术手术手术手术手术单中心的卡斯特曼病.

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