Primary localized amyloidoma of abdominal wall presenting as abscess: Rare case

M. Garg, Gurmeen Kaur, N. Mahajan, S. Goyal
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引用次数: 1

Abstract

The deposition of amyloid as a distinct, clinically apparent mass is uncommon particularly in the soft tissues. There have been no previously published case reports of abdominal wall involvement; thereby we are describing a case of AA amyloidoma which presented as an abdominal wall abscess without any evidence of systemic disease. The clinical and radiological findings suggested soft tissue abscess likely cysticercosis or a neoplastic process. This case demonstrates the importance of considering the possibility of amyloidoma in the differential diagnosis of soft tissue lesions.
腹壁原发性局部淀粉样瘤,表现为脓肿:罕见病例
淀粉样蛋白沉积作为一个明显的,临床上明显的肿块是罕见的,特别是在软组织。以前没有发表过腹壁受累的病例报告;因此,我们描述一个AA淀粉样瘤的病例,表现为腹壁脓肿,没有任何全身性疾病的证据。临床及影像学表现提示软组织脓肿可能为囊虫病或肿瘤。本病例显示了在软组织病变鉴别诊断中考虑淀粉样瘤可能性的重要性。
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