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Two Cases of Neonatal Lupus and Literature Review

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Abstract
Neonatal lupus is a rare rheumatic disease. Clinical manifestations include characteristic annular or macular rashes, congenital heart block, cytopenias, and hepatitis. Neonatal lupus is caused by transmission of maternal immunoglobulin G autoantibodies such as anti-SSA/Ro antibody or anti-SSB/La antibody to the fetus through the placenta. We report two cases of neonatal lupus. The first case refers to an 18-day-old male with annular rashes on both cheeks, neutropenia, positive tests for antinuclear antibody, anti-SSA/Ro antibody, and anti-SSB/La antibody. His mother was diagnosed with systemic lupus erythematosus characterized by positive tests for antinuclear antibody, anti-SSA/Ro antibody, and anti-SSB/La antibody. The second case represents a 32-day-old female with annular rash on both hands, soles, and the genital area, neutropenia, hepatitis, positive tests for antinuclear antibody, and anti-SSA/Ro antibody. Skin punch biopsy was conducted. Her mother did not have history of connective tissue diseases. We referred her mother to the division of rheumatology of the department of internal medicine. The mother was suspected with primary Sj횄쨋gren's syndrome because of arthralgia and dry eye symptoms with positive tests for antinuclear antibody, anti-SSA/Ro antibody, anti-SSB/La antibody, and rheumatoid factor. It is necessary to suspect neonatal lupus in neonates or infants with characteristic annular rash with or without maternal history of connective tissue disorders.
All Author(s)
D. H. Kim ; S. J. Lee ; T. H. Kim ; G. H. Yoo ; J. Y. Lee ; S. Y. Lee ; S. H. Chang ; H. J. Lee ; S. A. Hong ; J. S. Park
Issued Date
2018
Type
Article
Keyword
Neonatal lupusAutoantibodiesExanthema
Publisher
Soonchunhyang Medical Research Institute
ISSN
2233-4289 ; 2233-4297
Citation Title
Soonchunhyang Medical Science
Citation Volume
24
Citation Number
1
Citation Start Page
76
Citation End Page
80
Language(ISO)
eng
DOI
10.15746/sms.18.013
URI
http://schca-ir.schmc.ac.kr/handle/2022.oak/1058
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