Published online Jan 21, 2022. doi: 10.12998/wjcc.v10.i3.1016
Peer-review started: June 2, 2021
First decision: June 25, 2021
Revised: July 5, 2021
Accepted: December 22, 2021
Article in press: December 22, 2021
Published online: January 21, 2022
Processing time: 227 Days and 11.5 Hours
Sjogren’s syndrome (SS), which affect salivary gland function, is an autoimmune disease. SS may involve extraglandular organs. Approximately 10 to 20 percent of SS patients have clinically significant lung disease, but presentation of pulmonary amylodosis is extremly rare. The incidence of benign monoclonal gammopathy in SS patients is high, but multiple myeloma is rare. No case involving the simultaneous occurrence of two rare diseases, pulmonary amyloidosis and multiple myeloma, in the same patient with SS has been reported so far.
A 41-year-old male patient was referred to our hematology department due to incidentally detected gastric plasmacytoma. He had been diagnosed with SS four years earlier. Multiple miliary nodules, ground glass opacity in both lung fields, and enlargement of both inguinal lymph nodes was observed on chest and abdomen computer tomography. Based on the pathological findings of lung and lymph node biopsied specimens, the patient was diagnosed with pulmonary amyloidosis and multiple myeloma. Pulmonary amyloidosis and multiple myeloma associated with SS has rarely been reported.
This is an extremely rare case of simultaneous pulmonary amyloidosis and mul
Core Tip: Sjogren’s syndrome (SS) is known for its involvement in exocrine glands, and may also involve extraglandular organs. Interstitial lung disease is the most common pulmonary abnormality in primary SS, but pulmonary amyloidosis is rare. In addition, the incidence of benign monoclonal gammopathy in SS patients is relatively high, but multiple myeloma is very rare. Herein, we report the extremely rare case of simultaneous pulmonary amyloidosis and multiple myeloma in the same patient with SS.