نتایج جستجو برای: neonatal lupus erythematosus

تعداد نتایج: 123488  

Journal: :Postgraduate medical journal 1975
I P Mungall R V Hague

References DINES, D.E., CLAGETT, O.T. & GOOD, C.A. (1967) Nontuberculous pulmonary parenchymal conditions predisposing to spontaneous pneumothorax. Journal of Thoracic and Cardiovascular Surgery, 53, 726. DUBOIs, E.L. (1966) Lupus Erythematosus, p. 172. McGrawHill Book Company Inc., New York Blakiston Division. HOFFBRAND, B.l. & BECK, E.R. (1965) 'Unexplained' dyspnoea and shrinking lungs in sy...

Journal: :Acta reumatologica portuguesa 2017
Ana Raquel Teixeira Mariana Rodrigues Hercília Guimarães Cláudia Moura Iva Brito

Neonatal lupus (NL) is a very rare condition with an estimated incidence of 1 in 20.000 pregnancies. It is caused by the transplacental passage of autoantibodies anti-Ro/SSA, antiSa/SSB antibodies and/or anti-U1 RNP antibodies into the fetal circulation. The mother may be completely asymptomatic or have a known inflammatory rheumatic disease, such as Sjögren syndrome (SS) or Systemic Lupus Eryt...

Journal: :Irish medical journal 2011
C B Hackett M A McAleer B F O'Donnell

Neonatal lupus erythematosus (NLE) is an uncommon disease of the neonate. It is believed to be caused by the transplacental passage of maternal autoantibodies to the ribonucleoproteins (Ro/SSA, La/SSB or rarely U RNP) as these are almost invariably present in NLE sera. The most common clinical manifestations include cutaneous lupus lesions and congenital complete heart block. Hepatobiliary and ...

Journal: :Hong Kong medical journal = Xianggang yi xue za zhi 1997
W H Chow M S Lam W K Kwan W F Ng

Systemic lupus erythematosus is a multi-system inflammatory disease. The clinical manifestations are diverse. Hepatic manifestation is a rarely seen complication of systemic lupus erythematosus. We report a case of complication of systemic lupus erythematosus presenting as cholestatic hepatitis in a 56-year-old Chinese woman. The cholestatic hepatitis progressed as part of the lupus activity an...

2015
Karina de Oliveira Peliçari Mariana Postal Nailú Angelica Sinicato Fernando Augusto Peres Paula Teixeira Fernandes Roberto Marini Lilian Tereza Lavras Costallat Simone Appenzeller

OBJECTIVES To determine the serum interleukin-17 (IL-17) levels in childhood-onset systemic lupus erythematosus patients and to evaluate the association between IL-17 and clinical manifestations, disease activity, laboratory findings and treatment. METHODS We included 67 consecutive childhood-onset systemic lupus erythematosus patients [61 women; median age 18 years (range 11-31)], 55 first-d...

Journal: :Chest 1978
A I Kaplan F Zakher S Sabin

Pleural involvement in drug-induced lupus erythematosus is not uncommon. Lupus erythematosus cells were found in vivo in the pleural of an elderly patient who had received procainamide (Pronestyl) hydrochloride (2 gm daily) for nine months. Patients who initially have pleural effusions while receiving drugs capable of inducing lupus erythematosus should have the fluid analyzed for lupus erythem...

Background: Brucellosis is a zoonotic infection which is endemic in many countries. It is a multisystem disease which may present with a broad spectrum of clinical manifestations and complications. Neurobrucellosis is an uncommon complication of brucellosis. Case presentation: A 25-year-old woman with a history of lupus for 5 months referred to the emergency ward of Shahid Beheshti Hosp...

Journal: :Reumatologia clinica 2014
Rocío Porcel Chacón Leopoldo Tapia Ceballos Rocío Díaz Cabrera María Teresa Gutiérrez Perandones

Neonatal lupus erythematosus is an infrequent disease seen in newborns. It is caused by transplacental maternal autoantibody passage. Cutaneous involvement and congenital heart block (CHB) are the most common affections, although it may involve multiple organs like the liver, lungs, blood, nervous or digestive systems. This article present a review of the four cases diagnosed in the past five y...

Journal: :middle east journal of digestive diseases 0
neda nozari parisa divsalar

this case report demonstrates fatal gastrointestinal vasculitis as a rare presentation of systemic lupus erythematosus. a 34-year-old woman presented with abdominal pain and diarrhea. anti nuclear antibody was positive and high titre of anti-ds dna antibody was also reported. treatment with corticosteroid and supportive cares were started; however, her condition worsened. eventually, she was co...

Journal: :journal of research in medical sciences 0
babak tamizifar golnaz samadi maryam rismankarzadeh

hemophagocytic syndrome (hps) is an uncommon manifestation in systemic lupus erythematosus (sle). clinical features of hps include fever, pancytopenia, abnormal liver enzyme, hepatosplenomegaly, lymphadenopathy, and coagulation disorder. hps comprises primary and reactive forms. herein, we describe a case of untreated sle with hps as one of the first manifestations of systemic lupus.

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