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Nodular cutaneous amyloidoma of the extremity secondary to chronic granulomatous inflammation in setting of sarcoidosis

机译:结节病的慢性肉芽肿炎症的末端结节淀粉样蛋白瘤

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摘要

Soft tissue amyloidoma is a rare condition that presents primarily in the abdomen and/or mediastinum and more uncommonly on the extremities. Soft tissue amyloidomas on the extremities have been associated with chronic inflammation, particularly when accompanied by AA-type amyloid deposition as seen in local trauma, surgery, hypertension and diabetes. To our knowledge, this is the first reported case of nodular cutaneous amyloidoma in the setting of systemic and cutaneous sarcoidosis. A 65-year-old woman presented with an asymptomatic subcutaneous nodule above her left lateral malleolus. Histopathology of the lesion showed an inconspicuous epidermis with amorphous eosinophilic material deposited in masses within the entire dermis. Congo red and crystal violet stains were positive. Based on the clinical and pathologic findings she was diagnosed with nodular cutaneous amyloidoma. We hypothesize that this process developed secondary to the chronic granulomatous inflammation of sarcoidosis.
机译:软组织淀粉片瘤是一种罕见的病症,其主要在腹部和/或纵隔中呈现,并且在肢体上更罕见。 四肢上的软组织淀粉样蛋白瘤已经与慢性炎症有关,特别是当伴随局部创伤,手术,高血压和糖尿病中的AA型淀粉样蛋白沉积时。 据我们所知,这是第一个报告的全身和皮肤结节病的结节皮肤淀粉片瘤的病例。 一个65岁的女性在她的左侧麦芽糖之上呈现出无症状皮下结节。 病变的组织病理学表现出一种不显眼的表皮,其具有沉积在整个真皮内肿块中的无定形嗜酸性材料。 刚果红色和水晶紫色污渍是阳性的。 基于临床和病理发现,她被诊断出患有结节淀粉膜膜膜状炎。 我们假设这一过程开发了慢性肉芽肿的结节病炎症。

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