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腹盆腔Castleman 病的MSCT表现探讨

作者:田 路 刘建立 来洪建 张 英 刘英慧

所属单位:山东省菏泽市立医院 (山东 菏泽274000)

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摘要

目的探讨腹盆腔巨大淋巴结增 生症(CD)的MSCT表现及临床、病理特点。 方法 结合临床与手术病理资料,回顾分 析16例CD的MSCT表现特点。结果 16例 Castleman病患者,其中男6例,女10例, 年龄分别为10-73岁,平均年龄38.2岁。 病理上,16例CD,其中13例为透明血管 型,1例为混合型,2例为浆细胞型。16例 中均为局限型CD,表现为腹盆腔的单发 肿块,呈类圆形或椭圆形,直径在2.0- 11.0cm间,平均5.6cm,其中,2个肿块 见钙化,2个肿块内见点片状低密度坏死 灶,1个肿块内见裂隙状低密度灶,边界 清晰,其余肿块均呈均质密度伴显著持续 强化,且其中1个肿块内见粗大血管影, 增强程度和腹主动脉相似。结论 均质软 组织密度肿块伴显著持续强化及钙化、少 数见低密度影是局限性CD的主要CT表现, 具有一定的特征性。

Objective To investigate the MSCT manifestations and clinical, pathological features of the pelvic and abdominal giant lymph node hyperplasia (CD). Methods With the combination of clinical and surgical pathological information, had a retrospective analysis of the MSCT appearances among 16 cases of CD. Results 16 cases of Castleman patients, including 6 males, 10 females, whose age were 10 to 73 years old, and the average age is 38.2. Pathologically, 16 cases were localized type, including 13 cases of hyaline vascular type, 1 cases of mixed type, 2 cases were plasma cell type. In those 16 cases of localized CD, manifested as abdominal and pelvic solitary mass, which were round or oval, 2.0-11.0cm in diameter, average 5.6CM. Among them, 2 mass had calcification, 2 masses showed point sheet low density necrosis, the crack-like low density area could be seen in 1 mass. slit like clear boundaries homogeneous density, with significant continued to strengthen showed the rest mass, and 1 of them within the masses see thick blood film, the degree of enhancement and abdominal aorta similar. Conclusion Homogeneous soft tissue density mass with significant sustained enhancement and calcification, few see the low density are the main limitations of CT CD performance, has certain characteristics.

【关键词】巨淋巴结增生症;体层摄影术;X线计算机

【中图分类号】R711.33

【文献标识码】A

【DOI】10.3969/j.issn.1672-5131.2015.08.028

前言

巨大淋巴结增生症(Castleman disease,CD)又称血管滤泡性淋巴 组织增生,是一种非常罕见的、原因不明的良性淋巴结增生性疾病。 1954年Castleman等[1]在一群患有纵隔淋巴病的病人中发现此病,命名 为血管淋巴错构瘤或巨大淋巴结异常增生,进行了首次报道。CD组织 学分为三种主要类型:(1)透明血管型 (2)浆细胞型 (3)混合型。诸多 影像和病理文献中报道CD一般好发于胸部,但是近年来研究发现CD可 以发生在任何有淋巴组织的部位。目前关于位于腹盆腔的该病的CT表 现报道尚不多见,术前易误诊。笔者搜集有完整的CT资料并经手术病 理证实的CD 16例,结合临床、病理和以往文献分析讨论发生于腹盆腔 CD的CT特点,旨在提高对本病的认识。