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影像学表现酷似副脾的Castleman病:一例报告

Castleman disease mimicking accessory spleen on imaging: A case report.

作者信息

Yazdi Niloofar Ayoobi, MomeniAmjadi Arman, Kermanipour Rad Ghannadzadeh, Alizadeh Sajjad, Salahshour Faeze, Tahamtan Mohammadreza

机构信息

Advanced Diagnostic and Interventional Radiology Research Center (ADIR), Tehran University of Medical Sciences, Tehran, Iran.

School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Radiol Case Rep. 2024 Nov 11;20(1):651-656. doi: 10.1016/j.radcr.2024.09.143. eCollection 2025 Jan.

Abstract

Castleman disease (CD) is a nonclonal lymphoproliferative disorder that causes non-neoplastic lymph node enlargement. With an incidence of approximately 21-25 cases per million, CD presents variably, often mimicking both benign and malignant conditions across various body regions. Clinically, it ranges from asymptomatic lymph node enlargement in Unicentric Castleman's Disease (UCD) to aggressive, multicentric presentations affecting multiple organs. Accurate diagnosis relies on surgical pathology due to the disease's diverse clinical and imaging manifestations. We report a rare case of UCD in a 19-year-old male who presented with mild, nonspecific left upper quadrant pain. Initial examinations, including ultrasonography, computed tomography, and magnetic resonance imaging, showed a hypervascular retroperitoneal mass that was initially suspected to be an accessory spleen or pancreatic tail neuroendocrine tumor. Surgical resection and histopathological analysis established the diagnosis of hyaline-vascular type UCD. This case highlights the diagnostic challenges of UCD, particularly when presented in uncommon locations like the retroperitoneal peripancreatic region. Imaging often fails to conclusively differentiate CD from other vascular lesions, necessitating a histopathological evaluation. Prior case studies have also reported similar diagnostic challenges and the efficacy of surgical resection for treating UCD. This case report adds to the existing literature by outlining the diagnostic procedure and challenges associated with retroperitoneal UCD. This highlights the need for increased awareness, advanced imaging techniques, and histopathological confirmation to achieve accurate diagnosis and effective treatment. A multidisciplinary approach is critical in managing such complex cases, ultimately leading to favorable patient outcomes.

摘要

卡斯特曼病(CD)是一种非克隆性淋巴增殖性疾病,可导致非肿瘤性淋巴结肿大。CD的发病率约为每百万人口21 - 25例,其表现多样,常常在身体各个部位模仿良性和恶性病症。临床上,它的范围从单中心卡斯特曼病(UCD)的无症状淋巴结肿大到影响多个器官的侵袭性多中心表现。由于该疾病多样的临床和影像学表现,准确诊断依赖于手术病理学。我们报告一例罕见的19岁男性UCD病例,该患者表现为轻度、非特异性左上腹疼痛。包括超声、计算机断层扫描和磁共振成像在内的初步检查显示,腹膜后有一个高血管性肿块,最初怀疑是副脾或胰尾神经内分泌肿瘤。手术切除和组织病理学分析确诊为透明血管型UCD。该病例突出了UCD的诊断挑战,特别是当它出现在腹膜后胰周区域等不常见部位时。影像学检查往往无法明确区分CD与其他血管病变,因此需要进行组织病理学评估。先前的病例研究也报告了类似的诊断挑战以及手术切除治疗UCD的疗效。本病例报告通过概述与腹膜后UCD相关的诊断程序和挑战,为现有文献增添了内容。这凸显了提高认识、采用先进成像技术和进行组织病理学确认以实现准确诊断和有效治疗的必要性。多学科方法对于管理此类复杂病例至关重要,最终可带来良好的患者预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97ff/11585472/3918a39a8b4a/gr1.jpg

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