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Light chain deposition disease involving kidney and liver in a patient with IgD myeloma.


ABSTRACT:

Background

IgD multiple myeloma (MM) is a rare subtype of MM and light chain deposition disease (LCDD) outside the kidney is also a rare and has scarcely been reported. We report herein the details of the first reported case of LCDD involving the kidney and liver co-occurring with IgD myeloma.

Case presentation

A 66-year-old female with IgD MM presented with rapidly progressive acute renal failure, ascites and pleural effusion. Immunofluorescent study of revealed the characteristic linear deposition of Ig? light chain along the glomerular and tubular basement membrane in kidney. Electron microscopy showed the powdery electron-dense deposits along the tubular and glomerular basement membrane consistent with the diagnosis of LCDD. Laser microdissection followed by mass spectrometry identified only Ig? light chain with more than 95% probability confirm the diagnosis of ?-LCDD but not heavy/light chain deposition disease. Liver biopsy with immunofluorescence study revealed the linear deposition of Ig? chain along the perisinusoidal space indicating the hepatic involvement of ?-LCDD. The patient was successfully treated with combination therapy with bortezomib, cyclophosphamide, dexamethasone, and daratumumab.

Conclusions

This report emphasizes that prompt biopsy of affected organs and initiation of clone directed therapy led to the correct diagnosis and favorable outcome in patient with LCDD who has extrarenal involvement.

SUBMITTER: Tsushima T 

PROVIDER: S-EPMC7824927 | biostudies-literature | 2021 Jan

REPOSITORIES: biostudies-literature

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Light chain deposition disease involving kidney and liver in a patient with IgD myeloma.

Tsushima Takafumi T   Suzuki Tomo T   Terao Toshiki T   Miura Daisuke D   Narita Kentaro K   Takeuchi Masami M   Shimuzu Akira A   Matsue Kosei K  

BMC nephrology 20210123 1


<h4>Background</h4>IgD multiple myeloma (MM) is a rare subtype of MM and light chain deposition disease (LCDD) outside the kidney is also a rare and has scarcely been reported. We report herein the details of the first reported case of LCDD involving the kidney and liver co-occurring with IgD myeloma.<h4>Case presentation</h4>A 66-year-old female with IgD MM presented with rapidly progressive acute renal failure, ascites and pleural effusion. Immunofluorescent study of revealed the characteristi  ...[more]

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