Suppr超能文献

一种罕见的临床实体:巨大毛石。

A rare clinic entity: Huge trichobezoar.

作者信息

Hamidi Hidayatullah, Muhammadi Marzia, Saberi Bismillah, Sarwari Mohammad Arif

机构信息

Radiology Department, French Medical Institute for Children (FMIC), Kabul, Afghanistan.

Radiology Department, French Medical Institute for Children (FMIC), Kabul, Afghanistan.

出版信息

Int J Surg Case Rep. 2016;28:127-130. doi: 10.1016/j.ijscr.2016.09.039. Epub 2016 Sep 28.

Abstract

INTRODUCTION

Trichobezoar is a rare clinical entity in which a ball of hair amasses within the alimentary tract. It can either be found as isolated mass in the stomach or may extend into the intestine. Trichobezoars mostly occur in young females with psychiatric disorders such as trichophagia and trichotillomania.

CASE REPORT

Authors present a giant trichobezoar in an 18year old female presented with complaints of upper abdominal mass, epigastric area pain, anorexia and weight loss. The patient underwent trans-abdominal ultrasonography (USG), Computed tomography (CT), upper gastrointestinal endoscopy and subsequently laparotomy. USG was inconclusive due to non-specific findings. It revealed a thick echogenic layer with posterior dirty shadowing extending from the left sub-diaphragmatic area to the right sub hepatic region obscuring the adjacent structures. Abdominal CT images revealed a huge, well defined, multi-layered, heterogeneous, solid appearing, non-enhancing mass lesion in the gastric lumen extending from the gastric fundus to the pyloric canal. An endoscopic attempt was performed for removal of this intraluminal mass, but due to its large size, and hard nature, the endoscopic removal was unsuccessful. Finally the large trichobezoar was removed with open laparotomy.

CONCLUSION

Trichobezoars should be suspected in young females with long standing upper abdominal masses; as the possibility of malignancy is not very common in this age group. While USG is inconclusive, trichobezoar can be accurately diagnosed with CT. In patient with huge trichobezoar, laparotomy can be performed firstly because of big size and location of mass, and psychiatric recommendation should be made to prevent relapse of this entity.

摘要

引言

毛发石是一种罕见的临床病症,其中一团毛发在消化道内聚集。它既可以在胃中作为孤立的肿块被发现,也可能延伸至肠道。毛发石大多发生于患有拔毛癖和咬毛症等精神疾病的年轻女性。

病例报告

作者报告了一名18岁女性的巨大毛发石病例,该患者主诉上腹部肿块、上腹部疼痛、厌食和体重减轻。患者接受了经腹超声检查(USG)、计算机断层扫描(CT)、上消化道内镜检查,随后进行了剖腹手术。由于检查结果不具特异性,超声检查未能确诊。它显示从左膈下区域到右肝下区域有一层厚的回声层,并伴有后方模糊阴影,遮挡了相邻结构。腹部CT图像显示胃腔内有一个巨大的、边界清晰的、多层的、不均匀的、实性的、无强化的肿块,从胃底延伸至幽门管。尝试通过内镜切除这个腔内肿块,但由于其体积大且质地硬,内镜切除未成功。最后通过剖腹手术切除了巨大的毛发石。

结论

对于长期存在上腹部肿块的年轻女性,应怀疑毛发石;因为在这个年龄组中恶性肿瘤的可能性不太常见。虽然超声检查不能确诊,但毛发石可以通过CT准确诊断。对于巨大毛发石患者,由于肿块的大小和位置,可首先进行剖腹手术,并应给予精神方面的建议以防止该病症复发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87f9/5048628/353787b85250/gr1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验