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儿童低蛋白血症的罕见病例:警惕毛发石。

An Unusual Case of Hypoproteinemia in Childhood: Keep in Mind Trichobezoar.

作者信息

Stinco Mariangela, Montemaggi Alessandra, Noccioli Bruno, Resti Massimo, Grosso Salvatore, Trapani Sandra

机构信息

Pediatric Section, Department of Health Sciences, Meyer Children's University Hospital, University of Florence, Florence, Italy.

Pediatric Surgery Unit, Meyer Children's University Hospital, University of Florence, Florence, Italy.

出版信息

Front Pediatr. 2020 Mar 4;8:82. doi: 10.3389/fped.2020.00082. eCollection 2020.

Abstract

Protein-losing enteropathy (PLE) is a rare condition characterized by protein loss through the gastrointestinal tract, leading to hypo-proteinemia. Patients may be asymptomatic or present with variety of complications of hypoproteinemia (e.g., oedema, ascites, pleural, and cardial effusions). We describe a case report of a young girl suffering from behavioral disorder since childhood who presented with generalized oedema, hypoproteinaemia, and microcytic hypochromic anemia. In addition, the girl had an intervention for jejunal atresia and intestinal malrotation in her past medical history. Upper gastrointestinal endoscopy revealed a trichobezoar extending from stomach into the small bowel, thus classified as Rapunzel Syndrome (RS), causing mechanical obstruction of intestinal lumen and intestinal lymphatic drainage resulting in a protein-losing enteropathy (PLE). Trichobezoar was successfully removed by a surgical laparotomy resulting in resolution of symptoms and normalization of biochemical parameters. Possibly, previous surgery might have had an influence on intestinal dysmotility and trichobezoar formation. PLE is a very rare presenting symptom of RS, developing as result of intestinal obstruction caused by large trichobezoars. RS has to be considered in patients, especially adolescents, suffering from behavior disorder as trichotillomania and trichophagia. Surgical removal and nutritional supplementation are the gold treatment of large trichobezoar.

摘要

蛋白丢失性肠病(PLE)是一种罕见疾病,其特征是通过胃肠道丢失蛋白质,导致低蛋白血症。患者可能无症状,或出现各种低蛋白血症并发症(如水肿、腹水、胸腔积液和心包积液)。我们报告一例自幼患有行为障碍的年轻女孩,她出现全身性水肿、低蛋白血症和小细胞低色素性贫血。此外,该女孩既往有空肠闭锁和肠旋转不良的手术史。上消化道内镜检查发现一个从胃延伸至小肠的毛发石,因此被归类为长发公主综合征(RS),导致肠腔机械性梗阻和肠道淋巴引流受阻,从而引发蛋白丢失性肠病(PLE)。通过外科剖腹手术成功取出毛发石,症状得以缓解,生化指标恢复正常。先前的手术可能对肠道动力和毛发石形成有影响。PLE是RS一种非常罕见的表现症状,由大的毛发石引起肠梗阻所致。对于患有拔毛癖和食毛癖等行为障碍的患者,尤其是青少年,必须考虑到RS。手术切除和营养补充是治疗大毛发石的黄金方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f3d/7065258/aef9ac855484/fped-08-00082-g0001.jpg

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