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Reports of three cases with the initial presentation of mesenteric vasculitis in children with system lupus erythematous.
Liu, Yuan; Zhu, Jia; Lai, Jian Ming; Sun, Xue Feng; Hou, Jun; Zhou, Zhi Xuan; Yuan, Xin Yu.
Afiliação
  • Liu Y; Rheumatology Department of Capital Institute of Pediatrics, Beijing, China.
  • Zhu J; Rheumatology Department of Capital Institute of Pediatrics, Beijing, China.
  • Lai JM; Rheumatology Department of Capital Institute of Pediatrics, Beijing, China. laijm99@163.com.
  • Sun XF; Radiology Department of Capital Institute of Pediatrics, Beijing, China.
  • Hou J; Rheumatology Department of Capital Institute of Pediatrics, Beijing, China.
  • Zhou ZX; Rheumatology Department of Capital Institute of Pediatrics, Beijing, China.
  • Yuan XY; Radiology Department of Capital Institute of Pediatrics, Beijing, China.
Clin Rheumatol ; 37(1): 277-283, 2018 Jan.
Article em En | MEDLINE | ID: mdl-29019060
ABSTRACT
We reviewed three cases of systemic lupus erythematosus (SLE) in children with mesenteric vasculitis (LMV) as initial presentation and analysed their clinical characteristics to improve the understanding of this disease. Three patients with SLE were admitted to our hospital and initially presented with gastrointestinal symptoms. We retrospectively analysed their clinical data, including clinical presentations, laboratory results, images and short- and long-term treatment outcomes. (1) All three children were school-age girls. The patients were presented to our hospital with vomiting and abdominal pain as initial symptoms. The patients also had urinary symptoms, including proteinuria in three cases, ureteropelvic dilatation in two cases and hydronephrosis in one case. (2) The patients had various positive autoantibodies and a low complement level. Two of the patients had blood system involvement, and one had central nervous system symptoms. (3) All of the patients had active SLE (SLEDAI-2K score ≥ 5 points and moderate to severe degree 10-24). (4) Abdominal CT scans with contrast showed the 'target sign' of the intestinal wall in case 1, a slightly thickened intestinal wall and blurry mesentery in case 2, and the 'comb sign' of the margin mesenteric blood vessels in case 3. (5) All three patients responded promptly to steroid therapy. The patients' symptoms improved rapidly after treatment. LMV is a rare SLE complication. The lack of comprehensive understanding of LMV's clinical presentation makes it considerably challenging to diagnose. LMV is also a serious complication of SLE that is often accompanied by concurrent damage to other organs. LMV often occurs with active SLE but responds rapidly to glucocorticoid therapy. Therefore, in order to make early diagnosis and treatment, we suggest checking autoantibodies and abdominal CT scans with contrast when children present with gastrointestinal symptoms and the involvement of other organs, especially the urinary system.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vasculite / Dor Abdominal / Lúpus Eritematoso Sistêmico Tipo de estudo: Screening_studies Limite: Adolescent / Child / Female / Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vasculite / Dor Abdominal / Lúpus Eritematoso Sistêmico Tipo de estudo: Screening_studies Limite: Adolescent / Child / Female / Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article