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A Rare Coexistence of Retroperitoneal Pararenal Castleman's Disease with Focal Nodular Hyperplasia

机译:具有局灶性结节性增生的腹膜术治疗术术的罕见共存

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摘要

Castleman's disease is a distinct form of lymph node hyperplasia divided into a solitary and a multicentric type. The solitary type occurs most commonly in the mediastinum and is usually asymptomatic. We present a patient with Castleman's disease of the hyaline-vascular solitary type located in the retroperitoneum. The patient was a 38-year-old male, who presented to our hospital with fever. The imaging workup revealed a retroperitoneal mass, measuring 4 × 6 cm, located lateral to the aorta, inferior to the left renal artery and vein, and posterior to the left testicular vein. At workup, a solid hepatic lesion, 3 cm in diameter, located in the left lobe of the liver, segment IV, was also identified. Both lesions were surgically excised. The retroperitoneal tumor had the features of angiofollicular hyperplasia (Castleman's disease), hyaline-vascular type, whereas a diagnosis of focal nodular hyperplasia was made for the hepatic lesion. The patient is well at fourty months followup postoperatively. Surgical excision is the treatment of choice for unifocal Castleman's disease.
机译:Castleman的疾病是一种独特的淋巴结增生形式,分为孤独和多元型。孤立型最常发生在纵隔中,通常是无症状的。我们患者患有Castleman疾病的透明血管孤立型,位于逆转物中。患者是一名38岁的男性,曾经发烧过我们的医院。成像后处理揭示了腹膜后肿块,测量4×6cm,位于主动脉横向,左侧肾动脉和静脉,以及左睾丸静脉后部。还鉴定了在余处,还鉴定了位于肝脏左侧叶片的直径为3cm的固体肝脏病变。两种病变都在手术切除。腹膜瘤肿瘤具有血管造胶增生(Castleman病),透明血管型的特征,而肝脏病变对局灶性结节性增生的诊断。患者在术后40个月的跟进。手术切除是对小足卡群岛病的选择。

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