Published online Aug 6, 2024. doi: 10.12998/wjcc.v12.i22.5196
Revised: May 24, 2024
Accepted: June 12, 2024
Published online: August 6, 2024
Processing time: 86 Days and 21.3 Hours
Plasma cell myeloma (PCM) is characterized by hypercalcemia, renal impairment, anemia, and bone destruction. While pleural effusion, ascites, abdominal pain, and bloody stool are common manifestations of lung disease or gastrointestinal disorders, they are rarely observed in patients with PCM.
A 66-year-old woman presented with complaints of recurrent chest tightness, wheezing, and abdominal bloating accompanied by bloody stools. Computed tomography revealed pleural effusion and ascites. Pleural effusion tests showed inflammation, but the T-cell spot test and carcinoembryonic antigen were negative. Endoscopy showed colonic mucosal edema with ulcer formation and local intestinal lumen stenosis. Echocardiography revealed enlarged atria and reduced left ventricular systolic function. The diagnosis remained unclear. Further testing revealed elevated blood light chain lambda and urine immunoglobulin levels. Blood immunofixation electrophoresis was positive for immunoglobulin G lambda type. Smear cytology of the bone marrow showed a high proportion of plasma cells, accounting for about 4.5%. Histopathological examination of the bone marrow suggested PCM. Flow cytometry showed abnormal plasma cells with strong expression of CD38, CD138, cLambda, CD28, CD200, and CD117. Fluorescence in situ hybridization gene testing of the bone marrow suggested 1q21 gene amplification, but cytogenetic testing showed no clonal abnormalities. Colonic mucosa and bone marrow biopsy tissues were negative for Highman Congo red staining. The patient was finally diagnosed with PCM.
A diagnosis of PCM should be considered in older patients with pleural effusion, ascites, and multi-organ injury.
Core Tip: Plasma cell myeloma is a common hematologic disorder that typically presents with hypocalcemia, anemia, kidney damage, and bone destruction. However, some patients present it atypically, with symptoms from other systems as the main manifestation, making the diagnosis difficult. For patients with complex presentations, necessary tests should be gradually refined through a multidisciplinary approach to obtain an accurate diagnosis. Clinicians need to accumulate clinical experience to effectively diagnose such difficult cases.