Literature DB >> 18847172

Diagnostic workup for mixed connective tissue disease in childhood.

Joost F Swart1, Nico M Wulffraat.   

Abstract

Raynaud's phenomenon, fatigue and pain (myalgia and arthralgia) are important presenting symptoms of pediatric-onset mixed connective tissue disease. The difficulty is that many adolescent girls complain of pain along with fatigue without evidence for serious disease. However, in patients with Raynaud's phenomenon one should search for evidence of connective tissue diseases. Capillaroscopy could be helpful since capillary changes of the SD-type significantly correlate with future development of scleroderma spectrum disorders. Symptoms of MCTD change in most patients during the disease course: in general the inflammatory features that are also seen in systemic lupus erythematosus and juvenile dermatomyositis have the tendency to disappear over years, but Raynaud's phenomenon is persistent and scleroderma symptoms become progressively prominent. Long-lasting remission occurs only in a minority of patients, while the majority has mild disease activity. Mortality in children with MCTD is lower than in adults. Since a change of symptoms is in the nature of the disease, a thorough and frequent evaluation of children with (probable) MCTD is important to detect organ involvement, which should be treated at an early (pre-symptomatic) stage. We present a diagnostic workup scheme for children and adolescents with propable MCTD.

Entities:  

Mesh:

Year:  2008        PMID: 18847172

Source DB:  PubMed          Journal:  Isr Med Assoc J            Impact factor:   0.892


  9 in total

Review 1.  [Connective tissue diseases in adolescents].

Authors:  J Peitz; I Tantcheva-Poór
Journal:  Hautarzt       Date:  2016-04       Impact factor: 0.751

2.  Inflammatory conditions of the pediatric hand and non-inflammatory mimics.

Authors:  Leanne N Royle; Bernadette W Muthee; Daniel G Rosenbaum
Journal:  Pediatr Radiol       Date:  2021-08-20

3.  Fifteen-year experience of pediatric-onset mixed connective tissue disease.

Authors:  Yi-Ying Tsai; Yao-Hsu Yang; Hsin-Hui Yu; Li-Chieh Wang; Jyh-Hong Lee; Bor-Luen Chiang
Journal:  Clin Rheumatol       Date:  2009-09-16       Impact factor: 2.980

4.  Prevalence of Family History of Autoimmune Disorders in Juvenile Systemic Lupus Erythematosus.

Authors:  Parisa Ashournia; Payman Sadeghi; Nima Rezaei; Mohammad-Hassan Moradinejad; Vahid Ziaee
Journal:  Maedica (Bucur)       Date:  2018-03

5.  Mixed connective tissue disease presenting with progressive scleroderma symptoms in a 10-year-old girl.

Authors:  Joanna Latuśkiewicz-Potemska; Agnieszka Zygmunt; Małgorzata Biernacka-Zielińska; Jerzy Stańczyk; Elżbieta Smolewska
Journal:  Postepy Dermatol Alergol       Date:  2013-10-30       Impact factor: 1.837

Review 6.  Mucocutaneous manifestations in juvenile-onset systemic lupus erythematosus: a review of literature.

Authors:  Direkrit Chiewchengchol; Ruth Murphy; Steven W Edwards; Michael W Beresford
Journal:  Pediatr Rheumatol Online J       Date:  2015-01-05       Impact factor: 3.054

7.  Henoch-Schönlein purpura in a pediatric patient with lupus.

Authors:  Peng Hu; Bao Yu Huang; Dong Dong Zhang; Guang Mei Jiang; Si Yan Liu; Xun Xia; Jie Cai
Journal:  Arch Med Sci       Date:  2017-04-20       Impact factor: 3.318

Review 8.  Autoimmune hepatitis as a presenting manifestation of mixed connective tissue disease in a child. Case report and review of the literature.

Authors:  Katarina Sedej; Nataša Toplak; Marina Praprotnik; Boštjan Luzar; Jernej Brecelj; Tadej Avčin
Journal:  Pediatr Rheumatol Online J       Date:  2015-11-10       Impact factor: 3.054

9.  Clinical features and outcome of mixed connective tissue disease in developmental age - observational study from one center.

Authors:  Lidia Rutkowska-Sak; Piotr Gietka
Journal:  Reumatologia       Date:  2019-12-31
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.