Plummer-Vinson Syndrome and Role of Endoscopic Balloon Dilatation in a 4-Year-Old Child

Priyanka Sahajwani, Megha Rustagi, Shivangi Tetarbe, Ira Shah
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Abstract

Plummer-Vinson syndrome (PVS), also called Patterson-Kelly-Brown syndrome, is a rare cause of dysphagia in children. This syndrome is associated with single or multiple webs in the upper esophagus with frequent iron deficiency. PVS usually occurs in adults, particularly in Caucasian middle-aged women, in the fourth to seventh decade of life, and is rare in childhood. There are various theories about what causes PVS. One theory suggests that iron deficiency plays a crucial role in its development. Iron repletion often improves dysphagia, although some patients require esophageal dilatation or bougienage. Herein, we describe the case of a 4-year-old male child, having complaints of difficulty in swallowing solid food, diagnosed with PVS.
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普卢默-文森综合征和内镜下气囊扩张在4岁儿童中的作用
普卢默-文森综合征(PVS),也称为帕特森-凯利-布朗综合征,是儿童吞咽困难的罕见病因。该综合征与食管上部单个或多个腹膜有关,常伴有缺铁。PVS通常发生在成年人,特别是高加索中年妇女,在生命的第四个到第七个十年,在儿童期很少见。关于PVS的原因有各种各样的理论。一种理论认为缺铁在其发展中起着至关重要的作用。补铁可改善吞咽困难,但有些患者需要食管扩张或扩张术。在此,我们描述的情况下,一个4岁的男孩,有吞咽固体食物困难的投诉,诊断为PVS。
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