Amyloidosis presenting as a malignancy: Two case reports and key diagnostic clues

Naveen Kumar Kushwaha , Laleng Mawia Darlong , Sunil Pasricha , Prerna Garg , Prafull Kumar Gamit
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引用次数: 0

Abstract

Respiratory amyloidosis manifests in three forms: focal/diffuse tracheobronchial, nodular parenchymal, and diffuse parenchymal. Surgical treatment is typically reserved for localized nodular pulmonary amyloidosis, while bronchoscopic techniques, radiotherapy, and medical therapy are preferred for other forms based on the specific subtype. We present two cases of pulmonary amyloidosis that were initially misdiagnosed as malignant based on cytology and imaging studies, but were later confirmed as amyloidosis following surgical resection. These cases highlight the potential role of surgery in such scenarios, extending its therapeutic value beyond conventional indications, as documented in the literature.
淀粉样变表现为恶性肿瘤:两例报告和关键诊断线索
呼吸道淀粉样变性表现为三种形式:局灶性/弥漫性气管支气管、结节性实质和弥漫性实质。对于局限性结节性肺淀粉样变性,通常保留手术治疗,而对于其他基于特定亚型的形式,首选支气管镜技术,放疗和药物治疗。我们报告了两例肺淀粉样变,最初根据细胞学和影像学检查误诊为恶性,但后来在手术切除后证实为淀粉样变。这些病例强调了手术在这种情况下的潜在作用,将其治疗价值扩展到传统适应症之外,正如文献所记载的那样。
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