Arslan Dilsat Fırat, Inal Ekin, Isik Emine Göknur, Sanli Yasemin
From the Department of Nuclear Medicine, Istanbul University, Istanbul Medical Faculty, Istanbul, Turkey.
Clin Nucl Med. 2025 Mar 1;50(3):e192-e193. doi: 10.1097/RLU.0000000000005603. Epub 2024 Dec 6.
We present a case with systemic amyloidosis secondary to immunoglobulin light-chain amyloidosis (AL amyloidosis), which 18 F-FDG PET/CT and 99m Tc-PYP scintigraphy revealed amyloid deposition in the peritoneum, omentum, and mesentery. AL amyloidosis is characterized by the proliferation of clonal plasma cells and increased production and extracellular accumulation of immunoglobulin light chains, leading to organ malfunction. Even though AL amyloidosis can affect the gastrointestinal system, peritoneal involvement is rarely observed. PET/CT and SPECT/CT images showed moderate to slightly increased tracer uptake in affected organs.
我们报告一例继发于免疫球蛋白轻链淀粉样变性(AL淀粉样变性)的系统性淀粉样变性病例,18F-FDG PET/CT和99m Tc-PYP闪烁扫描显示腹膜、大网膜和肠系膜有淀粉样沉积。AL淀粉样变性的特征是克隆性浆细胞增殖以及免疫球蛋白轻链产生增加和细胞外积聚,导致器官功能障碍。尽管AL淀粉样变性可累及胃肠道系统,但很少观察到腹膜受累。PET/CT和SPECT/CT图像显示受累器官的示踪剂摄取中度至轻度增加。