一例罕见的伴有钙化的胸壁卡斯特曼病病例

Ikki Takada, Ryosuke Amemiya, Shotaro Ono, Keni Kou, Yukio Morishita, Norihiko Ikeda, Kinya Furukawa
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引用次数: 1

摘要

伴有胸壁钙化的 Castleman 病非常罕见,迄今也鲜有此类病例的报道。一名 57 岁的妇女因胸部计算机断层扫描发现左侧胸壁肿瘤伴钙化而转诊至我院。她的胸部磁共振成像结果显示为分裂瘤或单发纤维瘤,因此我们为诊断和治疗目的进行了手术。病理结果显示,伴有钙化的肿瘤被诊断为透明血管型卡斯特曼病。手术后,患者没有出现明显症状,并继续接受定期随访检查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Rare Case of Chest Wall Castleman's Disease with Calcification.

Castleman's disease with calcification of the chest wall is very rare, and there have been few reports of such cases to date. A 57-year-old woman was referred to our hospital for a tumor with calcification on her left lateral chest wall, which was detected on chest computed tomography. Findings of her chest magnetic resonance imaging suggested schwannoma or a solitary fibrous tumor, and therefore, we performed surgery for diagnostic and therapeutic purposes. Pathologically, the tumor with calcification was diagnosed as Castleman's disease of the hyaline-vascular type. After the surgery, the patient has had no obvious symptoms and continues to undergo regular follow-up examinations.

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