Literature DB >> 8408828

In utero acute graft-versus-host disease in a neonate with severe combined immunodeficiency.

G Alain1, C Carrier, L Beaumier, J Bernard, M Lemay, A Lavoie.   

Abstract

We describe a male neonate with severe combined immunodeficiency who at birth had acute graft-versus-host disease (GVHD) as a result of maternal-fetal transfusion during pregnancy. Several clinical signs helped establish this diagnosis. Findings of a skin biopsy specimen confirmed the diagnosis of acute GVHD. Immunologic evaluation disclosed an absence of T and B lymphocytes. Acute GVHD in severe combined immunodeficiency most often occurs during the first weeks of life; intrauterine occurrence is unusual.

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Year:  1993        PMID: 8408828     DOI: 10.1016/0190-9622(93)70257-t

Source DB:  PubMed          Journal:  J Am Acad Dermatol        ISSN: 0190-9622            Impact factor:   11.527


  2 in total

Review 1.  Neonatal erythroderma: differential diagnosis and management of the "red baby".

Authors:  P H Hoeger; J I Harper
Journal:  Arch Dis Child       Date:  1998-08       Impact factor: 3.791

2.  Neonatal erythroderma: diagnostic and therapeutic challenges.

Authors:  Sandipan Dhar; Raghubir Banerjee; Rajib Malakar
Journal:  Indian J Dermatol       Date:  2012-11       Impact factor: 1.494

  2 in total

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