Esophageal bezoar on peptic stenosis in a 7-year-old child

B. O., Meskini T, Berrani H, S. M, E. S, M. N
{"title":"Esophageal bezoar on peptic stenosis in a 7-year-old child","authors":"B. O., Meskini T, Berrani H, S. M, E. S, M. N","doi":"10.47690/wjghe.2021.3605","DOIUrl":null,"url":null,"abstract":"The term bezoar refers to foreign bodies found in the digestive tract. It results in a stagnation of ingested non-digestible substances. We report a case of an esophageal bezoar collected in the pediatric gastroenterology department of the children's hospital in RabatMOROCCO. This observation of an esophageal bezoar, the first in our institution, to our knowledge, confirms the rarity of the pathology. 7-year-old child, taken by his parents to the children's hospital of the university hospital in Rabat for total aphagia. His history shows: psychomotor retardation, followed for 2 years for peptic esophagitis complicated by peptic stenosis. The course was marked by total aphagia, early postprandial vomiting, and weight loss of 6 kg in 3 months. This symptomatology has been evolving for 2 months. Esophagogastroduodenal fibroscopy, using an 8.5mm pediatric fiberscope, revealed an esophageal bezoar made of tissues, fibers, hair, sponge, plastics and ropes. A multistage endoscopic extraction was performed, which extracted a 430g bezoar. After a complete cleansing of the esophagus, the esophagogastroduodenal exploration showed ascension of the gastric folds on retrovision, a gaping cardia, a hernial pouch, an esophageal caliber disparity of 25 cm to 20 cm of the dental arches with presence of mucous ulcerations and false membranes. After extraction, the child resumed his normal diet with no vomiting. a proton pump inhibitor and antibiotic therapy were prescribed. INTRODUCTION The term bezoar refers to foreign bodies found in the digestive tract. It results in a stagnation of ingested non-digestible substances, such as hair (trichobezoar), certain vegetable fibers (phytobezoar), concentrated dairy products (lactobezoar), more rarely certain drugs (pharmacobezoar). Its esophageal location is little reported in the literature, it is often secondary to a morphological and / or functional abnormality of the esophagus and is frequently involved. It usually concerns children or young adolescents with mental disorders [1]. We report a case of an esophageal bezoar collected in the pediatric gastroenterology department of the children's hospital in RabatMOROCCO. This observation of an esophageal bezoar, the first in our institution, to our knowledge, confirms the rarity of the pathology. PATIENT AND OBSERVATION 7-year-old child, taken by his parents to the children's hospital of the university hospital in Rabat for total aphagia. His history shows: psychomotor retardation, followed for 2 years for peptic esophagitis complicated by peptic stenosis. The course was marked by total aphagia, early postprandial vomiting, and weight loss of 6 kg in 3 months. This symptomatology has been evolving for 2 months. The admission exam noted: a pale patient. A weight of 12kg (3 DS), a height of 114cm (2DS). World J Gastroenterol Hepatol Endosc Volume: 3.6 1/3 Received Date: 10 Oct 2021 Accepted Date: 16 Oct 2021 Published Date: 22 Oct 2021 The biological assessment showed on the blood count: Hemoglobin at 6.3 g / dL with erythrocyte indices in favor of microcytic hypochromic anemia, leukocytes at 15200 / mm3, polymorphonuclear cells at 12200 / mm3, lymphocytes at 2000 / mm3. Blood sugar and CRP were within standards. Esophagogastroduodenal fibroscopy, using an 8.5mm pediatric fiberscope, revealed an esophageal bezoar made of tissues, fibers, hair, sponge, plastics and ropes (Figure 1). A multistage endoscopic extraction was performed, which extracted a 430g bezoar (Figure 2). After a complete cleansing of the esophagus, the esophagogastroduodenal exploration showed an ascension of the gastric folds on retrovision (Figure 3), a gaping cardia, a hernial pouch, an esophageal caliber disparity of 25 cm to 20 cm of the dental arches with presence of mucous ulcerations and false membranes (Figure 4). After extraction, the child resumed his normal diet with no vomiting. a proton pump inhibitor and antibiotic therapy were prescribed. Figure 1: Endoscopic images of an esophageal bezoar. Figure 2: Endoscopic bezoar extraction Figure 3: Endoscopic image showing an ascending gastric folds, a gaping cardia and a hernial pouch. World J Gastroenterol Hepatol Endosc Volume: 3.6 2/3 Figure 4: Endoscopic image of esophagitis with esophageal peptic stenosis. DISCUSSION The bezoar a rare affection in children, it represents 0.15% of gastrointestinal foreign bodies. Gastric localization is the most frequent. The particularity of our case is above all the esophageal location, which is often unusual and unrecognized. Psychomotor retardation is often seen in patients followed for psychological pathologies, in our case. [2]. Esophageal bezoars can be divided into two groups: primary which occur in the esophagus and secondary where gastric bezoars migrate to the esophagus [3]. cases of esophageal bezoars which have been reported in patients with a functional and / or morphological abnormality of the esophagus (systemic disease, hypertonia of the lower esophageal sphincter, myasthenia gravis, Guillain-Barre syndrome, diabetes, diffuse spasm disease, achalasia, surgery of the esophagus, stomach, peristalsis syndrome ...) [4, 6]. Our case is one of the few primary esophageal bezoars reported in the literature that caused peptic esophageal stenosis, resulting in vomiting and total aphagia. The esophageal bezoar is manifested by swallowing disorders (dysphagia). It is rarely revealed by dyspnea [7]. In our observation, the patient reported mainly aphagia, vomiting and weight loss. Once the diagnosis of esophageal bezoar is clinically evoked, it is necessary to confirm it by endoscopy, which remains the examination of choice in cases of proximal esogastric and intestinal location. It has both diagnostic and therapeutic interests. In our case, the lumen of the esophagus is narrow and the risk of aspiration of fragments during the procedure makes bezoars difficult to treat. Thus, it is more convenient to break up the bezoar into fragments in the stomach by overtube-assisted endoscopy for an esophageal bezoar when possible. Broken bezoar particles can be extracted or pushed into the small intestine. However, intestinal obstruction can occur if the large fragments migrate into the small intestine. Conservative medical treatment can be used in front of small bezoars. Coca-Cola washes and endoscopic procedures can be used with a success rate of 91.3% has been reported in the treatment of gastric bezoars [8]. However, larger bezoars, endoscopic intervention or even surgery may be necessary. CONCLUSION The bezoar is a disease rarely seen in children. Its location in the esophagus is unusual. It is favored by functional or motor disorders of the esophagus with multiple etiologies. Gastrointestinal endoscopy remains the examination of choice. Endoscopic or even surgical treatment significantly improves symptoms.","PeriodicalId":93828,"journal":{"name":"World journal of gastroenterology, hepatology and endoscopy","volume":"44 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"World journal of gastroenterology, hepatology and endoscopy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.47690/wjghe.2021.3605","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The term bezoar refers to foreign bodies found in the digestive tract. It results in a stagnation of ingested non-digestible substances. We report a case of an esophageal bezoar collected in the pediatric gastroenterology department of the children's hospital in RabatMOROCCO. This observation of an esophageal bezoar, the first in our institution, to our knowledge, confirms the rarity of the pathology. 7-year-old child, taken by his parents to the children's hospital of the university hospital in Rabat for total aphagia. His history shows: psychomotor retardation, followed for 2 years for peptic esophagitis complicated by peptic stenosis. The course was marked by total aphagia, early postprandial vomiting, and weight loss of 6 kg in 3 months. This symptomatology has been evolving for 2 months. Esophagogastroduodenal fibroscopy, using an 8.5mm pediatric fiberscope, revealed an esophageal bezoar made of tissues, fibers, hair, sponge, plastics and ropes. A multistage endoscopic extraction was performed, which extracted a 430g bezoar. After a complete cleansing of the esophagus, the esophagogastroduodenal exploration showed ascension of the gastric folds on retrovision, a gaping cardia, a hernial pouch, an esophageal caliber disparity of 25 cm to 20 cm of the dental arches with presence of mucous ulcerations and false membranes. After extraction, the child resumed his normal diet with no vomiting. a proton pump inhibitor and antibiotic therapy were prescribed. INTRODUCTION The term bezoar refers to foreign bodies found in the digestive tract. It results in a stagnation of ingested non-digestible substances, such as hair (trichobezoar), certain vegetable fibers (phytobezoar), concentrated dairy products (lactobezoar), more rarely certain drugs (pharmacobezoar). Its esophageal location is little reported in the literature, it is often secondary to a morphological and / or functional abnormality of the esophagus and is frequently involved. It usually concerns children or young adolescents with mental disorders [1]. We report a case of an esophageal bezoar collected in the pediatric gastroenterology department of the children's hospital in RabatMOROCCO. This observation of an esophageal bezoar, the first in our institution, to our knowledge, confirms the rarity of the pathology. PATIENT AND OBSERVATION 7-year-old child, taken by his parents to the children's hospital of the university hospital in Rabat for total aphagia. His history shows: psychomotor retardation, followed for 2 years for peptic esophagitis complicated by peptic stenosis. The course was marked by total aphagia, early postprandial vomiting, and weight loss of 6 kg in 3 months. This symptomatology has been evolving for 2 months. The admission exam noted: a pale patient. A weight of 12kg (3 DS), a height of 114cm (2DS). World J Gastroenterol Hepatol Endosc Volume: 3.6 1/3 Received Date: 10 Oct 2021 Accepted Date: 16 Oct 2021 Published Date: 22 Oct 2021 The biological assessment showed on the blood count: Hemoglobin at 6.3 g / dL with erythrocyte indices in favor of microcytic hypochromic anemia, leukocytes at 15200 / mm3, polymorphonuclear cells at 12200 / mm3, lymphocytes at 2000 / mm3. Blood sugar and CRP were within standards. Esophagogastroduodenal fibroscopy, using an 8.5mm pediatric fiberscope, revealed an esophageal bezoar made of tissues, fibers, hair, sponge, plastics and ropes (Figure 1). A multistage endoscopic extraction was performed, which extracted a 430g bezoar (Figure 2). After a complete cleansing of the esophagus, the esophagogastroduodenal exploration showed an ascension of the gastric folds on retrovision (Figure 3), a gaping cardia, a hernial pouch, an esophageal caliber disparity of 25 cm to 20 cm of the dental arches with presence of mucous ulcerations and false membranes (Figure 4). After extraction, the child resumed his normal diet with no vomiting. a proton pump inhibitor and antibiotic therapy were prescribed. Figure 1: Endoscopic images of an esophageal bezoar. Figure 2: Endoscopic bezoar extraction Figure 3: Endoscopic image showing an ascending gastric folds, a gaping cardia and a hernial pouch. World J Gastroenterol Hepatol Endosc Volume: 3.6 2/3 Figure 4: Endoscopic image of esophagitis with esophageal peptic stenosis. DISCUSSION The bezoar a rare affection in children, it represents 0.15% of gastrointestinal foreign bodies. Gastric localization is the most frequent. The particularity of our case is above all the esophageal location, which is often unusual and unrecognized. Psychomotor retardation is often seen in patients followed for psychological pathologies, in our case. [2]. Esophageal bezoars can be divided into two groups: primary which occur in the esophagus and secondary where gastric bezoars migrate to the esophagus [3]. cases of esophageal bezoars which have been reported in patients with a functional and / or morphological abnormality of the esophagus (systemic disease, hypertonia of the lower esophageal sphincter, myasthenia gravis, Guillain-Barre syndrome, diabetes, diffuse spasm disease, achalasia, surgery of the esophagus, stomach, peristalsis syndrome ...) [4, 6]. Our case is one of the few primary esophageal bezoars reported in the literature that caused peptic esophageal stenosis, resulting in vomiting and total aphagia. The esophageal bezoar is manifested by swallowing disorders (dysphagia). It is rarely revealed by dyspnea [7]. In our observation, the patient reported mainly aphagia, vomiting and weight loss. Once the diagnosis of esophageal bezoar is clinically evoked, it is necessary to confirm it by endoscopy, which remains the examination of choice in cases of proximal esogastric and intestinal location. It has both diagnostic and therapeutic interests. In our case, the lumen of the esophagus is narrow and the risk of aspiration of fragments during the procedure makes bezoars difficult to treat. Thus, it is more convenient to break up the bezoar into fragments in the stomach by overtube-assisted endoscopy for an esophageal bezoar when possible. Broken bezoar particles can be extracted or pushed into the small intestine. However, intestinal obstruction can occur if the large fragments migrate into the small intestine. Conservative medical treatment can be used in front of small bezoars. Coca-Cola washes and endoscopic procedures can be used with a success rate of 91.3% has been reported in the treatment of gastric bezoars [8]. However, larger bezoars, endoscopic intervention or even surgery may be necessary. CONCLUSION The bezoar is a disease rarely seen in children. Its location in the esophagus is unusual. It is favored by functional or motor disorders of the esophagus with multiple etiologies. Gastrointestinal endoscopy remains the examination of choice. Endoscopic or even surgical treatment significantly improves symptoms.
食管牛黄治疗7岁儿童消化性狭窄
牛黄是指在消化道中发现的异物。它会导致摄入的不可消化物质停滞不前。我们报告一例食道牛黄收集在儿童医院儿科消化内科在拉巴特摩洛哥。据我们所知,这是本院首次观察到食管牛黄,证实了这种病理的罕见性。7岁儿童,被父母带到拉巴特大学医院的儿童医院治疗完全失语症。病史显示:精神运动迟缓,消化性食管炎合并消化性狭窄,随访2年。整个疗程的特点是完全失语,早期餐后呕吐,3个月内体重减轻6公斤。这种症状已经发展了2个月。食管胃十二指肠纤维镜,使用8.5mm儿童纤维镜,发现由组织、纤维、头发、海绵、塑料和绳索组成的食管牛黄。进行多级内镜提取,提取430g牛黄。完全清洁食道后,食道-胃十二指肠探查显示逆行胃褶上升,贲门开口,疝囊,食道口径相差25厘米至20厘米,牙弓存在粘膜溃疡和假膜。拔牙后,患儿恢复正常饮食,无呕吐。给予质子泵抑制剂和抗生素治疗。牛黄是指在消化道中发现的异物。它导致摄入的不可消化物质停滞不前,如头发(毛牛黄),某些植物纤维(植物牛黄),浓缩乳制品(乳牛黄),更罕见的是某些药物(药牛黄)。它的食道位置在文献中很少报道,它通常继发于食管的形态和/或功能异常,并且经常累及。它通常涉及患有精神障碍的儿童或青少年[1]。我们报告一例食道牛黄收集在儿童医院儿科消化内科在拉巴特摩洛哥。据我们所知,这是本院首次观察到食管牛黄,证实了这种病理的罕见性。患者与观察7岁儿童,由父母带到拉巴特大学医院的儿童医院治疗完全失语症。病史显示:精神运动迟缓,消化性食管炎合并消化性狭窄,随访2年。整个疗程的特点是完全失语,早期餐后呕吐,3个月内体重减轻6公斤。这种症状已经发展了2个月。入院检查记录:一个脸色苍白的病人。体重12公斤(3ds),身高114厘米(2DS)。世界杂志胃肠醇肝醇内皮体积:3.6 1/3接收日期:2021年10月10日接收日期:2021年10月16日发表日期:2021年10月22日血液计数生物学评估显示:血红蛋白6.3 g / dL,红细胞指数倾向于小细胞性低色素贫血,白细胞15200 / mm3,多形核细胞12200 / mm3,淋巴细胞2000 / mm3。血糖、CRP均在标准范围内。食管胃十二指肠纤维镜,使用8.5mm儿童纤维镜,发现由组织、纤维、毛发、海绵、塑料和绳索组成的食管牛黄(图1)。进行多级内镜提取,提取430g牛黄(图2)。食管胃十二指肠探查显示逆行胃皱襞上升(图3),贲门开口,疝囊,食管胃粘膜,食管胃粘膜。食管口径相差25厘米至20厘米的牙弓,存在粘膜溃疡和假膜(图4)。拔牙后,儿童恢复正常饮食,无呕吐。给予质子泵抑制剂和抗生素治疗。图1:食管牛黄的内镜图像。图2:内镜下牛黄提取图3:内镜图像显示胃褶皱上升,贲门开口,疝囊。图4:食管炎伴食管消化性狭窄的内镜影像。牛黄在儿童中少见,仅占胃肠道异物的0.15%。胃定位是最常见的。本病例的特殊之处在于食道的位置,通常是不寻常和不被认识的。在我们的病例中,精神运动迟缓经常出现在心理疾病患者中。[2]. 食管牛黄可分为发生在食道的原发性牛黄和胃牛黄迁移至食道的继发性牛黄[3]。
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