# Systemic, asymptomatic skeletal muscle infiltration by MALT lymphoma: Defining a 'silent infiltrator' phenotype with 18F-FDG PET/CT

**Authors:** Yasuyuki Takahashi, Ken Naganuma, Yuka Tanaka, Noriyuki Sakata, Taisuke Kawada, Masahiro Kizaki, Shuji Momose, Morihiro Higashi, Takayuki Tabayashi

PMC · DOI: 10.1016/j.lrr.2026.100573 · Leukemia Research Reports · 2026-02-20

## TL;DR

A rare, non-destructive form of MALT lymphoma silently infiltrates muscles and bone marrow, detected by PET/CT and responding well to treatment.

## Contribution

Identifies a new 'silent infiltrator' variant of MALT lymphoma with asymptomatic muscle and marrow involvement.

## Key findings

- PET/CT detected high tumor burden with normal muscle enzymes, indicating non-destructive growth.
- Bendamustine-Rituximab therapy achieved complete metabolic response in the patient.
- The case highlights a unique, indolent clinical variant of muscular MALT lymphoma.

## Abstract

We report a rare phenotype of Stage IV extranodal marginal zone lymphoma (MALT lymphoma) manifesting as diffuse, asymptomatic skeletal muscle and bone marrow infiltration in a 60-year-old female. Despite a high tumor burden and intense ¹⁸F-FDG avidity (SUVmax 8.8), muscle enzymes remained normal, indicating a non-destructive "silent infiltrator" growth pattern. The diagnosis was confirmed via biopsy (CD20+, CD5-, CyclinD1-) and negative MYD88 L265P mutation status, excluding lymphoplasmacytic lymphoma. The patient achieved a Complete Metabolic Response following Bendamustine-Rituximab therapy. This case underscores the utility of PET/CT in detecting occult systemic disease and defines a unique, indolent clinical variant of muscular MALT lymphoma.

## Linked entities

- **Proteins:** MS4A1 (membrane spanning 4-domains A1), CD5 (CD5 molecule), ccnd1.S (cyclin D1 S homeolog), MYD88 (MYD88 innate immune signal transduction adaptor)
- **Chemicals:** Bendamustine (PubChem CID 65628)
- **Diseases:** MALT lymphoma (MONDO:0007650), lymphoplasmacytic lymphoma (MONDO:0000432)

## Full-text entities

- **Genes:** CD5 (CD5 molecule) [NCBI Gene 921] {aka LEU1, T1}, CCND1 (cyclin D1) [NCBI Gene 595] {aka BCL1, D11S287E, PRAD1, U21B31}, MYD88 (MYD88 innate immune signal transduction adaptor) [NCBI Gene 4615] {aka IMD68, MYD88D, WM1}, FCER2 (Fc epsilon receptor II) [NCBI Gene 2208] {aka BLAST-2, CD23, CD23A, CLEC4J, FCE2, FCErII}, BTK (Bruton tyrosine kinase) [NCBI Gene 695] {aka AGMX1, AT, ATK, BPK, IGHD3, IMD1}, LPL (lipoprotein lipase) [NCBI Gene 4023] {aka HDLCQ11, LIPD}, CMPK1 (cytidine/uridine monophosphate kinase 1) [NCBI Gene 51727] {aka CK, CMK, CMPK, UMK, UMP-CMPK, UMPK}, B2M (beta-2-microglobulin) [NCBI Gene 567] {aka AMYLD6, IMD43, MHC1D4}, IL2RB (interleukin 2 receptor subunit beta) [NCBI Gene 3560] {aka CD122, IL15RB, IMD63, P70-75}, KRT20 (keratin 20) [NCBI Gene 54474] {aka CD20, CK-20, CK20, K20, KRT21}, BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596] {aka Bcl-2, PPP1R50}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, MME (membrane metalloendopeptidase) [NCBI Gene 4311] {aka CALLA, CD10, CMT2T, NEP, SCA43, SFE}
- **Diseases:** IgM (MESH:D053306), systemic disease (MESH:D034721), DLBCL (MESH:D016403), sarcoma (MESH:D012509), WM (MESH:D008258), fever (MESH:D005334), necrosis (MESH:D009336), myositis (MESH:D009220), muscle injury (MESH:D009135), non-Hodgkin lymphomas (MESH:D008228), I (MESH:D006969), myalgia (MESH:D063806), lymphadenopathy (MESH:D008206), Lymphoplasmacytic Lymphoma (MESH:D008223), gastric lesion (MESH:D013272), lymphoepithelial lesions (MESH:D009059), B-cell neoplasm (MESH:D016393), IV (MESH:D006011), alopecia (MESH:D000505), marrow infiltration (MESH:D017254), Extranodal Marginal Zone Lymphoma (MESH:D018442), toxicity (MESH:D064420), weight loss (MESH:D015431), B (MESH:D006509), swelling (MESH:D004487), neurotoxicity (MESH:D020258), multiple myeloma (MESH:D009101), Hepatosplenomegaly (MESH:C535727), muscle weakness (MESH:D018908), monoclonal gammopathy (MESH:D010265), Stage IV disease (MESH:D007676), tumor (MESH:D009369), bone pain (MESH:D010146), disease (MESH:D004194), chronic inflammation (MESH:D007249), Follicular Lymphoma (MESH:D008224), hypermetabolism (MESH:C565498)
- **Chemicals:** 18F-FDG (MESH:D019788), Bendamustine (MESH:D000069461), Rituximab (MESH:D000069283), BR (MESH:D001966), R-CHOP (-)
- **Species:** Homo sapiens (human, species) [taxon 9606], Helicobacter pylori (species) [taxon 210]
- **Mutations:** L265P

## Full text

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## Figures

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## References

12 references — full list in the complete paper: https://tomesphere.com/paper/PMC12966862/full.md

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Source: https://tomesphere.com/paper/PMC12966862