2000
DOI: 10.1212/wnl.55.9.1379
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Henoch–Schönlein purpura and stroke: Antiphosphatidyl-ethanolamine antibody in CSF and serum

Abstract: A 15-year-old girl with features of Henoch-Schönlein purpura and brain infarct had a transient IgA antiphosphatidylethanolamine antibody (aPE) in her serum and CSF that disappeared 5 months after presentation. Serum aPE is known to be associated with thrombotic events. The authors found no aPE in the CSF of two control individuals or in the serum of two patients with active Henoch-Schönlein purpura without neurologic involvement. The patient may represent a variant of antiphospholipid antibody syndrome.

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Cited by 48 publications
(19 citation statements)
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“…Direct binding of monoclonal aPS to human trophoblast, inhibition of hCG production and blocking trophoblast invasiveness have been observed for plasma protein independent aPS (Katsuragawa et al, 1997;Di Simone et al, 2000). The aPE we observed in the CSF of a 15-year-old stroke patient was plasma protein independent (Sokol et al, 2000), and we have shown that certain aPL associated with early rejection of solid organ grafts were independent of plasma proteins (McIntyre and Wagenknecht, 2003). Indeed, the majority of CSF aPL described in this report 10/12 were classified as plasma protein independent.…”
Section: Discussionsupporting
confidence: 61%
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“…Direct binding of monoclonal aPS to human trophoblast, inhibition of hCG production and blocking trophoblast invasiveness have been observed for plasma protein independent aPS (Katsuragawa et al, 1997;Di Simone et al, 2000). The aPE we observed in the CSF of a 15-year-old stroke patient was plasma protein independent (Sokol et al, 2000), and we have shown that certain aPL associated with early rejection of solid organ grafts were independent of plasma proteins (McIntyre and Wagenknecht, 2003). Indeed, the majority of CSF aPL described in this report 10/12 were classified as plasma protein independent.…”
Section: Discussionsupporting
confidence: 61%
“…Indeed, there is evidence that some aPL detected in the central nervous system (CNS) may be synthesized in situ and not result from extravasation through the CNS-associated vasculature (MartinezCordero, 1997;Sokol et al, 2000;Baraczka et al, 2002). Although there are no published reports to confirm that intrathecally-produced aPL, do not escape into the systemic circulation and vice versa, locally produced aPL in the CNS might be responsible for some aPLassociated symptoms in otherwise aPL seronegative patients (Miret et al, 1997).…”
Section: Discussionmentioning
confidence: 99%
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“…In addition, the finding of aPE in the cerebral spinal fluid of patient with a documented ischemic stroke may suggest a possibility of an intrathecal production of aPL in the course of central nervous system disorders. However, this observation needs to be confirmed by further investigations (Sokol et al, 2000). A number of reports confirmed also an association between aPE and atherosclerosis.…”
Section: Selected Non-criteria Antiphospholipid Antibodies and Their mentioning
confidence: 88%