Author ORCID Identifier
https://orcid.org/0009-0006-7227-9866
Abstract
Hodgkin lymphoma (HL) is a kind of lymphatic malignancy distinguished by the presence of Reed-Sternberg cells. It often manifests as painless lymphadenopathy and systemic symptoms (B symptoms and can affect a variety of lymphoid tissues. The causes of HL are complicated and include genetic predisposition, environmental conditions and viral infections, particularly the Epstein-Barr virus (EBV). The diagnosis is primarily based on histological evaluation of lymph node samples, with immunophenotyping assisting classification. Herein, we report a case of classical Hodgkin’s lymphoma (HL) in an otherwise healthy 31-year-old male who had a mass per abdomen for a year and recently noticed a swelling in his left axilla. On ultrasound, abdominal lymphadenopathy and splenomegaly with multiple ill-defined hypoechoic lesions were identified. Lymph node biopsy revealed Erythroid hyperplasia with trilineage hematopoiesis, leading to a diagnosis of Hodgkins lymphoma.
Publication Date
2025
Publisher
JSS Academy of Higher Education & Research
Conflict of Interest
None
Keywords
Hodgkin's lymphoma, Abdominal lymphadenopathy, Splenomegaly, Erythroid hyperplasia with trilineage hematopoiesis
Word Count
966
Recommended Citation
Shankaralingam S, Nagaragatta V.
Lymphoma Chronicles: Insights from a Distinct Hodgkin's Lymphoma Case Report.
Digital Journal of Clinical Medicine.
2025;
7(2):
-.
doi:
https://doi.org/10.55691/2582-3868.1231
Creative Commons License
This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 4.0 License.
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