scholarly journals Synchronous skin lesions in mother and baby with neonatal lupus erythematosus

Author(s):  
Adrian Y. S. Lee ◽  
Alvin H. K. Tan ◽  
Catriona Brennan ◽  
Dimitra Beroukas ◽  
Tom P. Gordon ◽  
...  
1970 ◽  
Vol 44 (2) ◽  
pp. 84-86
Author(s):  
CE Ezeudu ◽  
OI Ezejiofor ◽  
WC Igwe ◽  
CC Ezechukwu ◽  
HM Nwankwo ◽  
...  

Systemic lupus erythematosus is a chronic inflammatory autoimmune disease that affects all organ systems and follows a relapsing and remitting course with presentation ranging from indolent to fulminant. It is an uncommon condition in children and usually manifests as the cutaneous form in the paediatric age group. We report a case of neonatal lupus erythematosus in a six-week-old Nigerian infant seen at NAUTH, Nnewi. The objective of this report is to highlight the existence of this very rare condition in infants. A 6-week-old female infant presented at the paediatric unit of our facility with a history of a pre-auricular skin eruptions of five weeks and poor suckling of three weeks duration. The skin lesions persisted unchanged after 14 days of antibiotics. A skin snip was taken for histology and a diagnosis of neonatal lupus erythematosus was made.Key words: neonatal lupsus erythematosus, infant, Nnewi.


2011 ◽  
Vol 73 (1) ◽  
pp. 19-22
Author(s):  
Akiko TARA ◽  
Takeshi OKAWA ◽  
Takuya INOUE ◽  
Noriyuki MISAGO ◽  
Yutaka NARISAWA ◽  
...  

2020 ◽  
Vol 13 (6) ◽  
pp. e233873
Author(s):  
Gopal Agrawal ◽  
Bincy Varghese ◽  
Manish Balde ◽  
Sanjay Wazir

Neonatal lupus erythematosus (NLE) should be considered when a newborn develops atrioventricular heart block along with the presence of autoantibodies to Sjogren’s syndrome autoantigens in the maternal serum. NLE can also present with features such as cutaneous lesions, hepatic dysfunction or haematological abnormalities. Differential diagnosis usually includes congenital infections as there is a significant overlap of symptoms with NLE. We report a case of NLE who had multiorgan involvement with macular erythematous skin lesions present at birth, and on investigation was found to have cytomegalovirus (CMV) infection. The diagnostic dilemma was whether to consider this infection as symptomatic or just colonisation. In the infant described, the absence of end organ damage specific to CMV infection (hearing loss, intracranial calcifications, retinitis, brain involvement) made a diagnosis of symptomatic CMV unlikely.


1994 ◽  
Vol 19 (5) ◽  
pp. 409-411 ◽  
Author(s):  
R.E. JENKINS ◽  
A.R. KURWA ◽  
D.J. ATHERTON ◽  
M.M. BLACK

1991 ◽  
Vol 18 (5) ◽  
pp. 333-338 ◽  
Author(s):  
B. Maynard ◽  
K. M. Leiferman ◽  
M.S. Peters

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