AI Article Synopsis
- * A 48-year-old woman exhibited hemophagocytic syndrome with involvement of her pituitary gland and neurological issues, prompting further investigation.
- * The diagnosis was confirmed through examination of perisplenic vessels, highlighting the need for comprehensive histopathological analysis when there is a strong suspicion of this type of lymphoma.
Article Abstract
Intravascular large B-cell lymphoma is a rare entity characterized by the proliferation of neoplastic lymphocytes in the lumen of small blood vessels and high mortality. Diagnosis of intravascular lymphoma is often delayed or established postmortem. Here, we report the case of a 48-year-old woman presenting hemophagocytic syndrome, with pituitary gland and neurological involvement. Diagnosis of intravascular large B-cell lymphoma was made on perisplenic vessels, while liver and bone marrow biopsy was noncontributive. This case demonstrates the importance of thorough histopathologic investigations in the setting of high suspicion.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6512020 | PMC |
| http://dx.doi.org/10.1155/2019/9625075 | DOI Listing |
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