Cerebral infarct with recurrence of hemolytic-uremic syndrome in a child following renal transplantation View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1992-11

AUTHORS

Manuel Mochon, Bruce A. Kaiser, J. P. de Chadarevian, Martin S. Polinsky, H. J. Baluarte

ABSTRACT

A white girl with a history of atypical hemolyticuremic syndrome (HUS) and persistent microangiopathic anemia, and thrombocytopenia for 2 months after the initial presentation at age 7 months, received her first cadaveric renal transplant at age 3 years. During the first 2.5 days post transplant, she developed progressive thrombocytopenia and anemia followed by tonic-clonic seizures and loss of consciousness, secondary to a diffuse cerebral infarction of the left hemisphere. Renal histology showed evidence of glomerular microthrombi and microangiopathy. A large cerebral infarct, previously described in patients during their initial presentation with HUS, presented in our patient as part of the recurrence of the disease post renal transplantation. More... »

PAGES

550-552

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf00866501

DOI

http://dx.doi.org/10.1007/bf00866501

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1029652469

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/1482644


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