ReviewBMC oral health2025
Primary giant mucosa-associated lymphoid tissue lymphoma of the lower lip: a case report and literature review.
Review in BMC oral health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
2 citing papers in PubMed.
- First Comprehensive Characterization of Lip Lymphoma: A Population-Based Study.Acta haematologica · 2026Article
- A scientometric study on research trends and characteristics of lymphoma involving the oral cavity.Journal of dental sciences · 2026Article
Corrections and comments
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Oral lymphomas are rare and difficult to diagnose, with Mucosa-Associated Lymphoid Tissue (MALT) lymphoma most commonly affecting older adults, particularly women. MALT lymphoma of the lip is exceptionally rare, and its cause is poorly understood. We present a case of primary giant MALT lymphoma of the lower lip, explore its clinicopathological features, and review relevant literature. An 83-year-old woman developed a painless, pea-sized swelling on the right lower lip over three years, which gradually increased in size without discomfort. She had no history of chronic infections or autoimmune diseases, and all investigations were unremarkable. Examination revealed a spherical, indurated mass on the left lower lip, measuring 8 cm, with no regional lymphadenopathy. Histology and immunohistochemistry confirmed extranodal marginal zone B-cell lymphoma of MALT. This case underscores the need to consider lymphoma in the differential diagnosis, even without systemic symptoms. Patients with oral MALT lymphoma often achieve complete remission after treatment, but diagnosing it can be challenging, requiring immunohistochemical testing for confirmation.
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