Non-Hodgkin's lymphoma revealed by a cerebral vascular stroke: A case report
Hemorrhagic lesions in CNS lymphoma are extremely rare. We report the case of a 75-year-old patient admitted to the emergency room following a classic hemorrhagic stroke. The CT scan showed a hyperdense tumor-like process with perilesional edema, the diagnosis reinforced by (MRI). The patient underw...
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Veröffentlicht in: | Annals of medicine and surgery 2022-03, Vol.75, p.103459, Article 103459 |
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Sprache: | eng |
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Zusammenfassung: | Hemorrhagic lesions in CNS lymphoma are extremely rare. We report the case of a 75-year-old patient admitted to the emergency room following a classic hemorrhagic stroke. The CT scan showed a hyperdense tumor-like process with perilesional edema, the diagnosis reinforced by (MRI). The patient underwent macroscopically total surgical excision and the anatomo pathological examination concluded a diffuse non-Hodgkin's B large cell lymphoma. The follow up was marked by a clear clinical improvement. Primary cerebral lymphomas can be polymorphic, so this diagnosis should always be kept in mind during stroke manifestations. This case illustrates the diagnostic difficulty of this rare and poor prognosis condition.
•Primary central nervous system (CNS) lymphoma is relatively rare, representing only 1%–2% of all primary CNS malignancies. Hemorrhagic lesions in CNS lymphoma are extremely rare.•This paper presents a case of A 75-year-old man admitted to the emergency room following a classic hemorrhagic stroke The CT scan showed a hyperdense tumor-like process with perilesional lesional edema, the diagnosis reinforced by (MRI). The patient underwent macroscopically total surgical excision and the anatomopathological examination concluded a diffuse non-Hodgkin's B large cell lymphoma. The follow up was marked by a clear clinical improvement.•The clinical expression of primary cerebral lymphomas can be polymorphic, so this diagnosis should always be kept in mind during stroke manifestations. This case illustrates the diagnostic difficulty of this rare and poor prognosis condition. |
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ISSN: | 2049-0801 2049-0801 |
DOI: | 10.1016/j.amsu.2022.103459 |