ArticleVirchows Archiv. A, Pathological anatomy and histopathology1987
T-cell lymphomas of the stomach: morphological and immunological studies characterizing two cases of T-cell lymphoma.
Article in Virchows Archiv. A, Pathological anatomy and histopathology, 1987. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.
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Who cites it
7 citing papers in PubMed, 1 synthesis or guideline pooled it, 31 citations in OpenAlex.
- Malignant neoplasms of the appendix.International journal of colorectal disease · 2007Pooled it
- Primary gastric T-cell lymphoma presenting with perforation: a case report and review of the literature.Journal of hematopathology · 2024Review
- Primary gastric T cell lymphoma mimicking marginal zone B cell lymphoma of mucosa-associated lymphoid tissue.Journal of hematopathology · 2008Article
- Primary gastric lymphoma.World journal of gastroenterology · 2004Review
- Primary gastric T-cell lymphoma accompanied by HTLV-I, HBV and H. pylori infection.Digestive diseases and sciences · 1999Review
- Rapidly growing primary gastric CD30 (Ki-1)-positive anaplastic large cell lymphoma.Digestive diseases and sciences · 1998Article
- Case report: primary CD30 (Ki-1)-positive anaplastic large cell lymphoma of the duodenum.Digestive diseases and sciences · 1996Review
Corrections and comments
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Authors and funding
3 authors at 1 institution in 1 country.
Funding
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Abstract
Using cytochemical, electron microscopic and immunohistochemical techniques in 20 primary malignant lymphomas of the stomach, we found 18 B-cell and 2 T-cell lymphomas. Primary T-cell lymphoma in the stomach has not been previously reported. The T cells in both cases were reminiscent of T immunoblasts with prominent nucleoli and a basophilic cytoplasm. Case 1 showed a cytological relationship to pleomorphic T-cell lymphoma, large cell type. Case 2 contained in addition some cells not previously described in T-cell lymphomas, resembling immature plasma cells with abundant rough endoplasmic reticulum. Focal positivity to acid phosphatase and dipeptidylaminopeptidase IV suggests the T-cell nature of both lymphomas. In both cases the tumour cells were OKT 11 and OKT 4 positive, and negative for OKT 8. Thus, both cases represent high-grade malignant T-cell lymphomas which correspond phenotypically to T-helper cell lymphoma. Case 2 revealed a further immunohistochemical peculiarity: atypical immunoblasts reacted positively with Ki-1 antibody. Thus, it is a Ki-1 lymphoma of T-cell type.
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