Intrapulmonary Castleman's Disease Pretending to Be a Lung Cancer-Work Up of an Intrapulmonary Tumour.

B. Haager, G. Kayser, S. Schmid, B. Passlick, S. Wiesemann
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引用次数: 4

Abstract

A 24 year old male presented with a history of recurrent bronchopulmonal infections. Chest computed tomography was performed, revealing a right central mass. In the following bronchoscopy and ultrasound guided needle aspiration of the tumour no specific diagnosis could be obtained. Due to the central location of the tumour thoracotomy and middle lobe resection was performed. Histopathological analysis revealed an intrapulmonary, subpleural located Morbus Castleman of the hyaline-vascular type.Castleman's disease is a very rare disorder of the lymphatic tissue that is differentiated into two clinical subtypes. The localized type presents histologically almost always as the hyaline-vascular form. Findings have been reported in mediastinal lymph nodes, the abdomen and peripheral lymphnodes. Intrapulmonary development is very rare and only 9 cases have previously been described in literature.On the other hand the multicentric type accounts for approximately 10%-15% of cases and histologically usually presents as the plasma cell variant. It is accompanied by fatigue and general weakness and often requires systemic steroid or chemotherapy.The localized type develops less clinical symptoms and is curable by complete surgical resection.
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肺内卡斯尔曼氏病伪装成肺癌——肺内肿瘤的伪装
24岁男性,既往有支气管肺部感染病史。胸部计算机断层扫描显示右侧中央肿块。在随后的支气管镜检查和超声引导下的肿瘤穿刺没有得到明确的诊断。由于肿瘤位于中心位置,我们进行了开胸和中肺叶切除术。组织病理学分析显示肺内,胸膜下位于透明血管型Morbus Castleman。Castleman病是一种非常罕见的淋巴组织疾病,临床分为两种亚型。局部型在组织学上几乎总是表现为透明血管型。在纵隔淋巴结、腹部和周围淋巴结均有报道。肺内发展是非常罕见的,只有9例以前的文献描述。另一方面,多中心型约占病例的10%-15%,组织学上通常表现为浆细胞变异。它伴随着疲劳和全身无力,通常需要全身类固醇或化疗。局部型临床症状较少,可通过完全手术切除治愈。
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