Watermelon stomach in a patient with primary Sjogren's syndrome

被引:3
作者
Krstic, Miodrag [1 ]
Alempijevic, Tamara [1 ]
Andrejevic, Sladjana [2 ]
Zlatanovic, Maja [3 ]
Damjanov, Nemanja [3 ]
Ivanovic, Branislava [4 ]
Jovanovic, Ivan [1 ]
Tarabar, Dino [5 ]
Milosavljevic, Tomica [1 ]
机构
[1] Clin Ctr Serbia, Clin Gastroenterol & Hepatol, Belgrade 11000, Serbia
[2] Clin Ctr Serbia, Inst Allergy & Clin Immunol, Belgrade 11000, Serbia
[3] Clin Ctr Serbia, Inst Rheumatol, Belgrade 11000, Serbia
[4] Clin Ctr Serbia, Inst Cardiovasc Dis, Belgrade 11000, Serbia
[5] Mil Med Acad, Gastroenterol Clin, Belgrade 11002, Serbia
关键词
sjogren's syndrome; gastral antral vascular ectasia; anemia; iron-deficiency; drug therapy; treatment outcome; ANTRAL VASCULAR ECTASIA; THERAPY;
D O I
10.2298/VSP1003256K
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction. Watermelon stomach ((WS)) or gastric antral vascular ectasia (GAVE) is a rare cause of upper gastrointestinal bleeding described in a variety of autoimmune disorders. Association of watermelon stomach with Sjogren's syndrome is extremely rare. Case report. We presented a 67-year old female with primary Sjogren's syndrome (SS) who had developed a persistent severe iron-deficiency anemia. An upper gastric endoscopy revealed the presence of gastric antral vascular ectasia (GAVE) as a cause of occult gastrointestinal bleeding. The treatment with argon-plasma coagulation was postponed as the conservative therapy with iron substitution and proton pump inhibitor led to improvement of anemia and hemoglobin levels normalization. Conclusion. This is the first report of WS in a patient with primary SS without the presence of coexisting autoimmune disorder. Recognition of this rare, but clinically important, cause of gastrointestinal bleeding may decrease comorbidity in patients with autoimmune disorders including primary Sjogren's syndrome.
引用
收藏
页码:256 / 258
页数:3
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