ArticleOncology letters2018
Classical Hodgkin lymphoma arising from heterotopic Warthin's tumor in the cervical lymph node: A case report.
Article in Oncology letters, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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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.
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Who cites it
6 citing papers in PubMed, 9 citations in OpenAlex.
- A Rare Diagnosis of Parotid Gland Follicular Lymphoma Arising in Warthin Tumor: Case Report and Literature Review.Medicina (Kaunas, Lithuania) · 2024Review
- Warthin tumor concomitant with mantle cell lymphoma: a case report and review of literature.Diagnostic pathology · 2024Review
- Article
- Prevalence of Lymphoid Neoplasia in a Retrospective Analysis of Warthin Tumor: A Single Institution Experience.Head and neck pathology · 2020Article
- Follicular Lymphoma Diagnosed in Warthin Tumor: A Case Report and Review of the Literature.Head and neck pathology · 2020Review
- Terminal deoxynucleotidyl transferase negative T-cell lymphoblastic lymphoma from heterotopic Warthin's tumor in cervical lymph nodes: a case report and review of literature.International journal of clinical and experimental pathology · 2019Article
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Authors and funding
2 authors at 2 institutions in 1 country.
Funding
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Abstract
Heterotopic Warthin's tumor (WT) arising from the cervical lymph nodes is uncommon and WT presenting concomitantly with classical Hodgkin's lymphoma has only been previously reported three times in English literature. The current study presents an unusual case of classical Hodgkin lymphoma (CHL) involving the heterotopic WT in a 59-year-old male. Histopathologic examination revealied a WT with extensive expansion of mixed-cellularity CHL in a lymph node in the right of the neck. Clinical staging was determined as stage IA disease. The patient received four courses of chemotherapy and local consolidative radiotherapy, no evidence of disseminated lymphoma was observed over the 6-month follow-up. To the best of our knowledge, this is the first well documented collision tumor between CHL and heterotopic WT of the cervical lymph nodes. The present case also expands the anatomical site of malignant lymphomas associated with WT.
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