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对一名患有Castleman病患者起源于肋骨的孤立性浆细胞瘤进行手术切除。

Surgical resection of a solitary plasmacytoma originating in a rib of a patient with Castleman's disease.

作者信息

Wilkinson Simon, Forrester-Wood Christopher P

机构信息

Department of Thoracic Surgery, Bristol Royal Infirmary, Bristol, United Kingdom.

出版信息

Ann Thorac Surg. 2003 Mar;75(3):1018-9. doi: 10.1016/s0003-4975(02)04476-4.

Abstract

Castleman's disease is a rare disorder characterized by lymphoid hyperplasia. It may present as asymptomatic involvement of one lymph node group or as a multicentric disease with systemic features. We report a patient with Castleman's disease who presented with axillary lymphadenopathy associated with a solitary plasmacytoma originating from a rib. The affected rib was surgically resected and radical radiotherapy was subsequently administered to the axillary lymph nodes. In this particular case, a joint surgical and oncologic approach resulted in a successful outcome.

摘要

卡斯特leman病是一种以淋巴组织增生为特征的罕见疾病。它可能表现为单个淋巴结组的无症状受累,或表现为具有全身特征的多中心疾病。我们报告一例卡斯特leman病患者,其表现为腋窝淋巴结病,伴有起源于肋骨的孤立性浆细胞瘤。对受累肋骨进行了手术切除,随后对腋窝淋巴结进行了根治性放疗。在这个特殊病例中,联合手术和肿瘤学方法取得了成功的结果。

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