# A Case of μ Heavy and λ Light Chain Amyloidosis in a Patient With Bi-Clonal (IgM κ and λ) Gammopathy Treated With Daratumumab

**Authors:** Armaan Dhaliwal, Ashish Tripathi, Soumiya Ravi

PMC · DOI: 10.7759/cureus.56994 · Cureus · 2024-03-26

## TL;DR

An elderly patient with a rare form of amyloidosis and bi-clonal gammopathy achieved a complete response after treatment with daratumumab.

## Contribution

This is the first reported case of μ heavy and λ light chain amyloidosis with bi-clonal gammopathy successfully treated with daratumumab.

## Key findings

- The patient achieved a complete hematological response after two cycles of daratumumab.
- Daratumumab led to a negative immunofixation study and reduced proteinuria.
- Prior treatment with CyBorD+R normalized the FLC ratio but did not eliminate M protein.

## Abstract

Our case report is of an elderly male with a history of IgM κ lymphoplasmacytic lymphoma (LPL) presenting with generalized neuropathy and weakness. Due to his LPL history and worsening renal function, he underwent a renal biopsy revealing the presence of μ heavy and λ light chains, revealing a diagnosis of amyloidosis with unbound heavy & light chains (AHL), a rare type of amyloidosis. His bone marrow biopsy demonstrated κ light chain restriction by flow cytometry and amyloid deposition. The patient’s serum had elevated free κ and λ light chains with a free light chain (FLC) ratio of 3.17. Serum immunofixation was positive for IgM κ and λ light chain clones. He completed six cycles of cyclophosphamide, bortezomib, dexamethasone, and rituximab (CyBorD+R), normalizing the FLC ratio. Still, he continued to present with persistently elevated M protein, IgM κ, and λ light chains on immunofixation. Thereafter, daratumumab, a human monoclonal antibody directed against CD38 expressed on myeloma cells was initiated, which led to a negative immunofixation study after two cycles accompanied by a reduction in protein excretion in the urine. The patient achieved a complete hematological response with daratumumab. To date, our case is the only reported μ heavy and λ light chain amyloidosis patient with bi-clonal (IgM κ and λ) gammopathy to be successfully treated with daratumumab.

## Linked entities

- **Proteins:** CD38 (CD38 molecule)
- **Chemicals:** cyclophosphamide (PubChem CID 2907), bortezomib (PubChem CID 387447), dexamethasone (PubChem CID 5743)
- **Diseases:** amyloidosis (MONDO:0019065), neuropathy (MONDO:0005244)

## Full-text entities

- **Genes:** MYOM2 (myomesin 2) [NCBI Gene 9172] {aka TTNAP}, CD38 (CD38 molecule) [NCBI Gene 952] {aka ADPRC 1, ADPRC1, cADPR1}
- **Diseases:** weakness (MESH:D018908), myeloma (MESH:D009101), neuropathy (MESH:D009422), IgM kappa lymphoplasmacytic lymphoma (MESH:D008223), Amyloidosis (MESH:D000686), amyloid deposition (MESH:D058225), Gammopathy (MESH:D010265), excretion (MESH:C565904)
- **Chemicals:** CyBorD+R (-), Daratumumab (MESH:C556306), dexamethasone (MESH:D003907), bortezomib (MESH:D000069286), rituximab (MESH:D000069283), cyclophosphamide (MESH:D003520)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

13 references — full list in the complete paper: https://tomesphere.com/paper/PMC11045342/full.md

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Source: https://tomesphere.com/paper/PMC11045342