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Pleural effusion, ascites, colon ulcers and hematochezia: What we can learn from the diagnostic process of a patient with plasma cell myeloma: A case report. | LitMetric

Pleural effusion, ascites, colon ulcers and hematochezia: What we can learn from the diagnostic process of a patient with plasma cell myeloma: A case report.

World J Clin Cases

Department of Gastroenterology, The First Affiliated Hospital of Shandong First Medical University, Shandong Provincial Qianfoshan Hospital, Jinan 250014, Shandong Province, China.

Published: August 2024

AI Article Synopsis

  • Plasma cell myeloma (PCM) is a disease that can cause high calcium levels, kidney problems, anemia, and damage to bones, but sometimes it can also cause rare symptoms like lung and stomach issues.
  • A 66-year-old woman had chest tightness, wheezing, and stomach bloating with bloody stools, leading to various tests to find out what was wrong.
  • After many tests, doctors discovered she had an increase in abnormal plasma cells in her bone marrow, which helped diagnose her with PCM.

Article Abstract

Background: 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.

Case Summary: 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 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.

Conclusion: A diagnosis of PCM should be considered in older patients with pleural effusion, ascites, and multi-organ injury.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11238796PMC
http://dx.doi.org/10.12998/wjcc.v12.i22.5196DOI Listing

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