Suggestive Diagnostic Process in a Case of Multiple Myeloma with Gastrointestinal Immunoglobulin Light-Chain Amyloidosis Accompanied by Protein-Losing Enteropathy

Author:

Endo Katsuya1ORCID,Ito Takehito1,Nomura Jun2,Murakami Keigo3,Kondo Shiho1,Satoh Tomonori1,Fukushi Daisuke1,Yoshino Yuki1,Sasaki Yoshiteru1,Takasu Atsuko1,Kogure Takayuki1,Hirota Morihisa1,Meguro Takayoshi1,Murakami Kazuhiro3,Kameoka Junichi2,Satoh Kennichi1

Affiliation:

1. Division of Gastroenterology, Tohoku Medical and Pharmaceutical University School of Medicine, Sendai, Miyagi, Japan

2. Division of Hematology, Tohoku Medical and Pharmaceutical University School of Medicine, Sendai, Miyagi, Japan

3. Division of Pathology, Tohoku Medical and Pharmaceutical University School of Medicine, Sendai, Miyagi, Japan

Abstract

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.

Publisher

Hindawi Limited

Subject

General Engineering

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