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Synchronous brain and intravascular B-cell lymphoma after remission of an adult hemophagocytic syndrome.


ABSTRACT: Hemophagocytic lymphohistiocytosis (HLH) should be considered in the differential diagnosis of adult patients with white matter disease. Brain involvement can be life-threatening and should prompt aggressive therapy. Even after HLH remission, the possibility of subsequent deterioration due to emergence of an aggressive intravascular lymphoma is highlighted here.

SUBMITTER: Fonseca VR 

PROVIDER: S-EPMC4831375 | biostudies-other | 2016 Apr

REPOSITORIES: biostudies-other

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