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Neoadjuvant radiotherapy of primary irresectable unicentric Castleman's disease: a case report and review of the literature

机译:原发性不可切除的单中心Castleman病的新辅助放疗:一例报道并文献复习

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Background Castleman disease (CD) is a rare benign disorder characterised by hyperplasia of lymphoid tissue that may develop at a single site or throughout the body. The etiology of this disorder is unclear, although the histopathological presentation can be differentiated into a hyaline vascular variant, a plasma cell variant and a mixed variant. Clinically, it has been recorded that 3 manifestations of CD are characterized: a localized unicentric type, a generalized multicentric type and a mixed form. Surgery remains the main treatment for resectable unicentric CD, since removal of the large node is possible without further complications. No consensus has been reached concerning the most adequate treatment for irresectable unicentric CD. Methods Case report of a 67 year old woman. Results This report, describes the case of a 67-year-old woman with unicentric Castleman disease located in the right lower abdomen. The patient had symptoms of fatigue, dyspnoea and pain in the right lower abdomen. Computed tomography (CT)- examination revealed a tumour, which had grown to form a close relationship with the common iliac vessels and the sacral bone. A Laparotomy procedure revealed that the tumour was an irresectable mass. Neo-adjuvant radiotherapy (40 Gy) was administered in order to downsize the tumour. Six weeks later a new CT-scan revealed a major reduction of the tumour, which enabled a successful radical resection of the tumour to be performed. Histopathological analysis of the tumour showed the hyaline vascular type of CD. Conclusions Neo-adjuvant radiotherapy should be considered in case of an irresectable unicentric CD.
机译:背景技术Castleman病(CD)是一种罕见的良性疾病,其特征是淋巴样组织增生,可能在单个部位或全身发生。尽管组织病理学表现可分为透明血管变体,浆细胞变体和混合变体,但该病的病因尚不清楚。在临床上,已经记录了CD的3种表现特征:局部单中心型,广义多中心型和混合形式。手术仍是可切除单中心CD的主要治疗方法,因为可以切除大结节而无进一步的并发症。对于不可切除的单中心CD的最适当治疗,尚未达成共识。方法一名67岁女性的病例报告。结果本报告描述了一名67岁的女性,其右下腹部患有单中心性Castleman病。该患者右小腹有疲劳,呼吸困难和疼痛的症状。计算机断层扫描(CT)检查显示肿瘤,该肿瘤已成长为与the总血管和the骨形成紧密联系。开腹手术显示该肿瘤为不可切除的肿块。为了缩小肿瘤大小,进行了新辅助放疗(40 Gy)。六周后,新的CT扫描显示肿瘤明显减少,这使得能够成功进行根治性切除。肿瘤的组织病理学分析显示为CD的透明血管类型。结论不可切除的单中心CD患者应考虑新辅助放疗。

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