Table of Contents
Definition / general | Case reports | Treatment | Gross images | Microscopic (histologic) description | Microscopic (histologic) images | Molecular / cytogenetics descriptionCite this page: MALT lymphoma. PathologyOutlines.com website. http://www.pathologyoutlines.com/topic/colontumorMALT.html. Accessed July 14th, 2017.
Definition / general
- Rare in colon
- Usually adults
- Often relapses but usually only in GI tract
Case reports
- 67 year old man with lymphomatoid polyposis (Am J Gastroenterol 1999;94:2540)
- 75 year old woman (World J Gastroenterol 2006;12:5573)
Treatment
- Early tumors are focal and curable by surgery
- Antibiotics may cause regression (J Gastroenterol 2005;40:843, Endoscopy 2002;34:343)
Microscopic (histologic) description
- Small atypical lymphocytes with irregular nuclei, lymphoepithelial lesions
- Reactive germinal centers and plasmacytic cells are common
Can be graded as:
- Grade 0: Normal - plasma cells in lamina propria, no lymphoid follicles
- Grade 1: Chronic active inflammation - lymphocyte clusters in lamina propria, no follicles and no lymphoepithelial lesions
- Grade 2: Chronic active inflammation with florid lymphoid follicle formation - prominent follicles with surrounding mantle zone and plasma cells, no lymphoepithelial lesions
- Grade 3: Suspicious lymphoid infiltrate in lamina propria, probably reactive - follicles surrounded by lymphocytes that infiltrate diffusely in lamina propria and / or epithelium
- Grade 4: Suspicious lymphoid infiltrate in lamina propria, probably lymphoma - follicles surrounded by centrocyte-like, marginal zone cells that infiltrate diffusely in lamna propria and epithelium
- Grade 5: Marginal zone (MALT) lymphoma - dense diffuse infiltrate of centrocyte-like, marginal zone cells in lamina propria with prominent lymphoepithelial lesions
Post therapy grading:
- Complete histologic remission:
- Absent or scattered plasma cells and small lymphoid cells in the lamina propria
- No lymphoepithelial lesions
- Normal or empty lamina propria and / or fibrosis
- Probable minimal residual disease:
- Aggregates of lymphoid cells or lymphoid nodules in the lamina propria and / or muscularis mucosa and / or submucosa
- No lymphoepithelial lesions
- Empty lamina propria and / or fibrosis
- Responding residual disease:
- Dense, diffuse or nodular extending around glands in the lamina propria
- Lymphoepithelial lesions, may or may not be present
- Focal empty lamina propria and / or fibrosis
- No response:
- Dense, diffuse or nodular lymphoid infiltrates
- Lymphoepithelial lesions, may or may not be present
- No changes in the stroma
Microscopic (histologic) images
Molecular / cytogenetics description
- Usually trisomy 3 or 18, less commonly t(1;14)(p22;q32, Gut 2006;55:1581 or t(11;18)(q21;q21) in 15% (Mod Pathol 2003;16:1232)
- T(11;18) produces API2-MALT1 fusion gene; these tumors usually occur in males and are larger with more advanced stage
- API2-MALT1 negative tumors usually occur in females






