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Plasma cell myeloma initially diagnosed as light-chain deposition disease on liver biopsy: A case report and literature review
Light-chain deposition disease (LCDD) is a rare condition characterized by the abnormal deposition of monoclonal light chains (LCs) in multiple organs, leading to progressive organ dysfunction. Herein, we report a case of plasma cell myeloma initially diagnosed as LCDD on liver biopsy performed for...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Lippincott Williams & Wilkins
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10063314/ https://www.ncbi.nlm.nih.gov/pubmed/37000077 http://dx.doi.org/10.1097/MD.0000000000033406 |
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author | Jeong, Ji Yun Yang, Hyeon Tae Cho, Seung Hyun Lee, Yu Rim Kim, Jinhee Kang, Min Kyu Hong, Jihoon Moon, Joon Ho Seo, An Na |
author_facet | Jeong, Ji Yun Yang, Hyeon Tae Cho, Seung Hyun Lee, Yu Rim Kim, Jinhee Kang, Min Kyu Hong, Jihoon Moon, Joon Ho Seo, An Na |
author_sort | Jeong, Ji Yun |
collection | PubMed |
description | Light-chain deposition disease (LCDD) is a rare condition characterized by the abnormal deposition of monoclonal light chains (LCs) in multiple organs, leading to progressive organ dysfunction. Herein, we report a case of plasma cell myeloma initially diagnosed as LCDD on liver biopsy performed for prominent cholestatic hepatitis. PATIENT CONCERNS: A 55-year-old Korean man complained of dyspepsia as the main symptom. On abdominal computed tomography performed at another hospital, the liver showed mildly decreased and heterogeneous attenuation with mild periportal edema. Preliminary liver function tests revealed abnormal results. The patient was treated for an unspecified liver disease; however, his jaundice gradually worsened, prompting him to visit our outpatient hepatology clinic for further evaluation. Magnetic resonance cholangiography revealed liver cirrhosis with severe hepatomegaly of unknown cause. A liver biopsy was performed for the diagnosis. Hematoxylin and eosin staining revealed diffuse extracellular amorphous deposits in perisinusoidal spaces with compressed hepatocytes. The deposits, which morphologically resembled amyloids, were not stained by Congo red but stained strongly positive for kappa LCs and weakly positive for lambda LCs. DIAGNOSES: Therefore, the patient was diagnosed with LCDD. Further systemic examination revealed a plasma cell myeloma. INTERVENTIONS: Fluorescence in situ hybridization, cytogenetics, and next-generation sequencing tested in bone marrow showed no abnormalities. The patient initially received bortezomib/lenalidomide/dexamethasone as the treatment regimen for plasma cell myeloma. OUTCOMES: However, he died shortly thereafter because of coronavirus disease 2019 complications. LESSONS: This case demonstrates that LCDD may present with sudden cholestatic hepatitis and hepatomegaly, and may be fatal if patients do not receive appropriate and timely treatment because of delayed diagnosis. Liver biopsy is useful for the diagnosis of patients with liver disease of unknown etiology. |
format | Online Article Text |
id | pubmed-10063314 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-100633142023-03-31 Plasma cell myeloma initially diagnosed as light-chain deposition disease on liver biopsy: A case report and literature review Jeong, Ji Yun Yang, Hyeon Tae Cho, Seung Hyun Lee, Yu Rim Kim, Jinhee Kang, Min Kyu Hong, Jihoon Moon, Joon Ho Seo, An Na Medicine (Baltimore) 4500 Light-chain deposition disease (LCDD) is a rare condition characterized by the abnormal deposition of monoclonal light chains (LCs) in multiple organs, leading to progressive organ dysfunction. Herein, we report a case of plasma cell myeloma initially diagnosed as LCDD on liver biopsy performed for prominent cholestatic hepatitis. PATIENT CONCERNS: A 55-year-old Korean man complained of dyspepsia as the main symptom. On abdominal computed tomography performed at another hospital, the liver showed mildly decreased and heterogeneous attenuation with mild periportal edema. Preliminary liver function tests revealed abnormal results. The patient was treated for an unspecified liver disease; however, his jaundice gradually worsened, prompting him to visit our outpatient hepatology clinic for further evaluation. Magnetic resonance cholangiography revealed liver cirrhosis with severe hepatomegaly of unknown cause. A liver biopsy was performed for the diagnosis. Hematoxylin and eosin staining revealed diffuse extracellular amorphous deposits in perisinusoidal spaces with compressed hepatocytes. The deposits, which morphologically resembled amyloids, were not stained by Congo red but stained strongly positive for kappa LCs and weakly positive for lambda LCs. DIAGNOSES: Therefore, the patient was diagnosed with LCDD. Further systemic examination revealed a plasma cell myeloma. INTERVENTIONS: Fluorescence in situ hybridization, cytogenetics, and next-generation sequencing tested in bone marrow showed no abnormalities. The patient initially received bortezomib/lenalidomide/dexamethasone as the treatment regimen for plasma cell myeloma. OUTCOMES: However, he died shortly thereafter because of coronavirus disease 2019 complications. LESSONS: This case demonstrates that LCDD may present with sudden cholestatic hepatitis and hepatomegaly, and may be fatal if patients do not receive appropriate and timely treatment because of delayed diagnosis. Liver biopsy is useful for the diagnosis of patients with liver disease of unknown etiology. Lippincott Williams & Wilkins 2023-03-31 /pmc/articles/PMC10063314/ /pubmed/37000077 http://dx.doi.org/10.1097/MD.0000000000033406 Text en Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | 4500 Jeong, Ji Yun Yang, Hyeon Tae Cho, Seung Hyun Lee, Yu Rim Kim, Jinhee Kang, Min Kyu Hong, Jihoon Moon, Joon Ho Seo, An Na Plasma cell myeloma initially diagnosed as light-chain deposition disease on liver biopsy: A case report and literature review |
title | Plasma cell myeloma initially diagnosed as light-chain deposition disease on liver biopsy: A case report and literature review |
title_full | Plasma cell myeloma initially diagnosed as light-chain deposition disease on liver biopsy: A case report and literature review |
title_fullStr | Plasma cell myeloma initially diagnosed as light-chain deposition disease on liver biopsy: A case report and literature review |
title_full_unstemmed | Plasma cell myeloma initially diagnosed as light-chain deposition disease on liver biopsy: A case report and literature review |
title_short | Plasma cell myeloma initially diagnosed as light-chain deposition disease on liver biopsy: A case report and literature review |
title_sort | plasma cell myeloma initially diagnosed as light-chain deposition disease on liver biopsy: a case report and literature review |
topic | 4500 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10063314/ https://www.ncbi.nlm.nih.gov/pubmed/37000077 http://dx.doi.org/10.1097/MD.0000000000033406 |
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