1977
DOI: 10.1001/archderm.113.4.477
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Phenytoin-induced pseudolymphoma syndrome: an immunologic study

Abstract: In vitro and in vivo immunologic studies were performed on a 28-year-old woman with phenytoin sodium-induced pseudolymphoma syndrome. During the acute phase of the syndrome, the patient appeared immunologically depressed. Six months after resolution of lymphadenopathy, repeat studies demonstrated a return to immunologic competence. In vitro studies of the patient's lymphocytes when incubated with phenytoin failed to indicate a delayed hypersensitivity reaction to the drug; These findings suggest that the patie… Show more

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Cited by 13 publications
(6 citation statements)
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“…Severe lymphadenopathy associated with antiepileptic drugs is well documented and very few cases have been described as pseudolymphoma in patients taking phenytoin, carbamazepine, lamotrigine, and ethosuximide. [2][3][4][5][6] Our patient presented symptoms extremely similar to the ones described by Masruha et al, 6 except for the duration of treatment before symptoms (2 weeks vs. 3 months). Both patients did not present liver abnormalities and had excellent prognosis after the drug was tapered off.…”
Section: Discussionsupporting
confidence: 84%
“…Severe lymphadenopathy associated with antiepileptic drugs is well documented and very few cases have been described as pseudolymphoma in patients taking phenytoin, carbamazepine, lamotrigine, and ethosuximide. [2][3][4][5][6] Our patient presented symptoms extremely similar to the ones described by Masruha et al, 6 except for the duration of treatment before symptoms (2 weeks vs. 3 months). Both patients did not present liver abnormalities and had excellent prognosis after the drug was tapered off.…”
Section: Discussionsupporting
confidence: 84%
“…in 1950 1 . Its pathogenesis has not been clearly understood, but it has been described as a hypersensitivity reaction due to anticonvulsants 2,3 . Clinically it is characterized by findings such as erythematous patch, maculopapular eruption or nodules developing within 2–3 weeks after administering causative agents, and systemic fever of 38–39 °C, lymphadenopathy, arthralgia, hepatosplenomegaly, abnormal liver profile and eosinophilia.…”
mentioning
confidence: 99%
“…No Sezary cells were seen in the peripheral blood. In all of these cases and in the case described by Charlesworth [24], mycosis-fungoides-like pseudolymphoma syndrome regressed after cessation of therapy.…”
mentioning
confidence: 71%