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Pediatr Dermatol ; 30(4): e63-4, 2013.
Article in English | MEDLINE | ID: mdl-22957833

ABSTRACT

We present the case of a 3-month-old child with probable catastrophic antiphospholipid syndrome who, after initial successful management with immunomodulary therapies including rituximab, experienced a cutaneous relapse. This rare event was successfully re-treated with repeated administration of rituximab, supporting its role in the control of this disorder. Dermatologic manifestations may be the main clinical presentation of antiphospholipid syndrome, a possible underdiagnosed but potentially fatal pathology.


Subject(s)
Antibodies, Monoclonal, Murine-Derived/therapeutic use , Antiphospholipid Syndrome/drug therapy , Antiphospholipid Syndrome/immunology , Immunologic Factors/therapeutic use , Humans , Infant , Male , Necrosis/drug therapy , Necrosis/immunology , Rituximab , Secondary Prevention , Severity of Illness Index , Treatment Outcome
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