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A newborn with grouped facial skin lesions and subsequent seizures
BACKGROUND: Congenital grouped skin lesions are alarming signs of a variety of threatening diagnoses of quite different origin. The present case report shows an impressive clinical pattern of a neonate and illustrates the difficulty in differential diagnosis of mixed connective tissue disease and ne...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4041904/ https://www.ncbi.nlm.nih.gov/pubmed/24884686 http://dx.doi.org/10.1186/1471-2431-14-126 |
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author | Döring, Michaela Rohrer, Karin Melanie Tsiflikas, Ilias Buchenau, Wolfgang Wilke, Marko Handgretinger, Rupert Poets, Christian Friedrich Goelz, Rangmar |
author_facet | Döring, Michaela Rohrer, Karin Melanie Tsiflikas, Ilias Buchenau, Wolfgang Wilke, Marko Handgretinger, Rupert Poets, Christian Friedrich Goelz, Rangmar |
author_sort | Döring, Michaela |
collection | PubMed |
description | BACKGROUND: Congenital grouped skin lesions are alarming signs of a variety of threatening diagnoses of quite different origin. The present case report shows an impressive clinical pattern of a neonate and illustrates the difficulty in differential diagnosis of mixed connective tissue disease and neonatal lupus erythematosus in newborns. This reported case is to our knowledge the first description of an unrecognized mixed connective tissue disease in the mother with an unusual clinical manifestation in the newborn, comprising skin lesions, neurological damage and non-typical antibody constellation. CASE PRESENTATION: We report on a Caucasian female neonate from a perinatally asymptomatic mother, who presented with grouped facial pustular-like skin lesions, followed by focal clonic seizures caused by multiple ischemic brain lesions. Herpes simplex virus infection was excluded and both the mother and her infant had the antibody pattern of systemic lupus erythematosus and neonatal lupus erythematosus, respectively. However, clinical signs in the mother showed overlapping features of mixed connective tissue disease. CONCLUSION: This case report emphasizes congenital Lupus erythematosus and mixed connective tissue disease as important differential diagnoses of grouped skin lesions in addition to Herpes simplex virus-infection. The coexistence of different criteria for mixed connective tissue disease makes it difficult to allocate precisely maternal and congenital infantile disease. |
format | Online Article Text |
id | pubmed-4041904 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40419042014-06-04 A newborn with grouped facial skin lesions and subsequent seizures Döring, Michaela Rohrer, Karin Melanie Tsiflikas, Ilias Buchenau, Wolfgang Wilke, Marko Handgretinger, Rupert Poets, Christian Friedrich Goelz, Rangmar BMC Pediatr Case Report BACKGROUND: Congenital grouped skin lesions are alarming signs of a variety of threatening diagnoses of quite different origin. The present case report shows an impressive clinical pattern of a neonate and illustrates the difficulty in differential diagnosis of mixed connective tissue disease and neonatal lupus erythematosus in newborns. This reported case is to our knowledge the first description of an unrecognized mixed connective tissue disease in the mother with an unusual clinical manifestation in the newborn, comprising skin lesions, neurological damage and non-typical antibody constellation. CASE PRESENTATION: We report on a Caucasian female neonate from a perinatally asymptomatic mother, who presented with grouped facial pustular-like skin lesions, followed by focal clonic seizures caused by multiple ischemic brain lesions. Herpes simplex virus infection was excluded and both the mother and her infant had the antibody pattern of systemic lupus erythematosus and neonatal lupus erythematosus, respectively. However, clinical signs in the mother showed overlapping features of mixed connective tissue disease. CONCLUSION: This case report emphasizes congenital Lupus erythematosus and mixed connective tissue disease as important differential diagnoses of grouped skin lesions in addition to Herpes simplex virus-infection. The coexistence of different criteria for mixed connective tissue disease makes it difficult to allocate precisely maternal and congenital infantile disease. BioMed Central 2014-05-22 /pmc/articles/PMC4041904/ /pubmed/24884686 http://dx.doi.org/10.1186/1471-2431-14-126 Text en Copyright © 2014 Döring et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Döring, Michaela Rohrer, Karin Melanie Tsiflikas, Ilias Buchenau, Wolfgang Wilke, Marko Handgretinger, Rupert Poets, Christian Friedrich Goelz, Rangmar A newborn with grouped facial skin lesions and subsequent seizures |
title | A newborn with grouped facial skin lesions and subsequent seizures |
title_full | A newborn with grouped facial skin lesions and subsequent seizures |
title_fullStr | A newborn with grouped facial skin lesions and subsequent seizures |
title_full_unstemmed | A newborn with grouped facial skin lesions and subsequent seizures |
title_short | A newborn with grouped facial skin lesions and subsequent seizures |
title_sort | newborn with grouped facial skin lesions and subsequent seizures |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4041904/ https://www.ncbi.nlm.nih.gov/pubmed/24884686 http://dx.doi.org/10.1186/1471-2431-14-126 |
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