Endo Katsuya, Ito Takehito, Nomura Jun, Murakami Keigo, Kondo Shiho, Satoh Tomonori, Fukushi Daisuke, Yoshino Yuki, Sasaki Yoshiteru, Takasu Atsuko, Kogure Takayuki, Hirota Morihisa, Meguro Takayoshi, Murakami Kazuhiro, Kameoka Junichi, Satoh Kennichi
Division of Gastroenterology, Tohoku Medical and Pharmaceutical University School of Medicine, Sendai, Miyagi, Japan.
Division of Hematology, Tohoku Medical and Pharmaceutical University School of Medicine, Sendai, Miyagi, Japan.
Case Rep Gastrointest Med. 2021 May 27;2021:5533993. doi: 10.1155/2021/5533993. eCollection 2021.
Multiple myeloma is a type of plasma cell neoplasm that produces monoclonal immunoglobulin. Multiple myeloma is known to cause immunoglobulin light-chain (AL) amyloidosis, which frequently involves the kidney and heart. Bone pain or fractures caused by osteolytic lesions and physical disorders related to renal or cardiac AL amyloidosis are major initial symptoms in multiple myeloma. Multiple myeloma diagnosed from the gastrointestinal symptoms is rare. We report a case of an 80-year-old man with multiple myeloma accompanied by gastrointestinal AL amyloidosis and secondary protein-losing enteropathy. The diagnostic process was suggestive, in that diarrhea and refractory leg edema related to protein-losing enteropathy were the primary symptoms and the trigger for making a sequential diagnosis of gastrointestinal AL amyloidosis and underlying multiple myeloma. This case is highly suggestive, in that multiple myeloma with gastrointestinal AL amyloidosis should be considered one of the background diseases of protein-losing enteropathy.
多发性骨髓瘤是一种产生单克隆免疫球蛋白的浆细胞肿瘤。已知多发性骨髓瘤可导致免疫球蛋白轻链(AL)淀粉样变性,常累及肾脏和心脏。溶骨性病变引起的骨痛或骨折以及与肾脏或心脏AL淀粉样变性相关的身体紊乱是多发性骨髓瘤的主要初始症状。由胃肠道症状诊断出的多发性骨髓瘤很少见。我们报告一例80岁男性,患有多发性骨髓瘤并伴有胃肠道AL淀粉样变性和继发性蛋白丢失性肠病。诊断过程具有提示性,因为与蛋白丢失性肠病相关的腹泻和难治性腿部水肿是主要症状,也是相继诊断胃肠道AL淀粉样变性和潜在多发性骨髓瘤的触发因素。该病例具有高度提示性,因为伴有胃肠道AL淀粉样变性的多发性骨髓瘤应被视为蛋白丢失性肠病的背景疾病之一。