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Concurrent gastric MALT and Hodgkin lymphoma: a case report
Kuniyuki Oka1, Reizo Nagayama, Nobuo Yonekawa
1Department of Pathology, Mito Saiseikai General Hospital, Mito, Ibaraki, Japan. oka-k@gb3.so-net.ne.jp
Insights
This case report details a rare instance of concurrent gastric extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue (MALT lymphoma) and classical Hodgkin lymphoma (CHL) in a single patient. The study explores potential origins, including MALT lymphoma transformation or de novo CHL development.
Area of Science:
- Oncology
- Gastroenterology
- Hematopathology
Background:
- Gastric extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue (MALT lymphoma) is a B-cell neoplasm originating in the stomach.
- Classical Hodgkin lymphoma (CHL) is a distinct lymphoid malignancy characterized by Hodgkin/Reed-Sternberg cells.
- Concurrent presentation of these two distinct lymphomas is exceptionally rare.
Observation:
- A 60-year-old male presented with concurrent gastric MALT lymphoma and CHL.
- Histopathological examination revealed atypical lymphoid cells in the gastric mucosa forming lymphoepithelial lesions, admixed with Hodgkin/Reed-Sternberg cells.
- Immunohistochemistry confirmed distinct cellular markers for MALT lymphoma (CD20+, CD79a+, PAX5+, BOB.1+) and CHL (CD30+, CD15+, EBV-encoded RNA+, EBV-LMP1+).
Findings:
- The MALT lymphoma involved the gastric mucosa to the muscular layer.
- Hodgkin/Reed-Sternberg cells were present within the MALT lymphoma background.
- Only the CHL component showed invasion into regional lymph nodes.
Implications:
- This case highlights the diagnostic challenges in differentiating concurrent lymphomas.
- Two potential etiological pathways are considered: MALT lymphoma transformation into CHL or de novo CHL arising within a background of MALT lymphoma.
- Further research is needed to elucidate the precise relationship and pathogenesis of these co-occurring gastric lymphomas.
Abstract:
This report describes a 60-year-old man with concurrent gastric extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue (MALT lymphoma) and classical Hodgkin lymphoma (CHL). Atypical, medium-sized, lymphoid cells proliferated in the mucosa to muscular layer of the stomach showing a lymphoepithelial lesion; admixed with Hodgkin/Reed-Sternberg (HRS) cells and an inflammatory cell background. MALT lymphoma cells expressed CD20, CD79a, PAX5, and BOB.1, and HRS cells expressed CD30, CD15, Epstein-Barr virus-encoded RNA, and EBV-latent membrane protein 1. Only CHL invaded into the regional lymph nodes. Two possibilities of transformation of MALT lymphoma into CHL and de novo CHL within MALT lymphoma are discussed.
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