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非特异性胃肠道症状作为节细胞神经母细胞瘤的首发症状——病例报告及文献综述

Nonspecific Gastrointestinal Symptoms as the First Sign of Ganglioneuroblastoma Intermixed-Case Report and Literature Review.

作者信息

Lipiński Łukasz, Lipińska Justyna, Kowalczuk Maria, Kopeć Izabela, Woźniak Magdalena Maria, Mitek-Palusińska Joanna, Mitura-Lesiuk Małgorzata

机构信息

Students' Scientific Society at the Department of Pediatric Radiology, Medical University of Lublin, 20-093 Lublin, Poland.

Department of Pediatric Radiology, Medical University of Lublin, 20-093 Lublin, Poland.

出版信息

J Clin Med. 2023 Sep 21;12(18):6092. doi: 10.3390/jcm12186092.

Abstract

Nonspecific gastrointestinal symptoms remain a problem for pediatricians because, out of a thousand trivial cases, there are rare diseases that require in-depth diagnostics and extensive knowledge to identify them. These complaints may be caused by a neoplastic process. We present the case of a 5-year-old boy whose diagnostic pathway lasted about 3 months. He was admitted to hospital due to severe abdominal pain. Physical examination revealed a bloated, hard, and painful abdomen. In the standing X-ray, the features of intestinal obstruction were visualized. An ultrasound examination showed a possible malignant lesion in the location of the left adrenal gland. After the surgical removal of the pathological mass and histopathological examination, the diagnosis of ganglioneuroblastoma intermixed was made. This tumor, along with neuroblastoma, ganglioneuroma, and ganglioneuroblastoma nodular, belongs to neuroblastic tumors (NTs), which originate from primitive cells of the sympathetic nervous system. NTs are quite rare, but they are still the majority of extracranial solid tumors in children, and their symptoms often appear relatively late when the neoplastic process is already advanced. The purpose of this review is to present current information about ganglioneuroblastoma, with a special emphasis on nonspecific gastrointestinal symptoms as first sign of this tumor and its diagnostics.

摘要

非特异性胃肠道症状仍然是儿科医生面临的一个问题,因为在一千个普通病例中,存在需要深入诊断和广泛知识才能识别的罕见疾病。这些症状可能由肿瘤性病变引起。我们介绍一名5岁男孩的病例,其诊断过程持续了约3个月。他因严重腹痛入院。体格检查发现腹部肿胀、坚硬且疼痛。站立位X线检查显示有肠梗阻特征。超声检查显示左肾上腺部位可能存在恶性病变。手术切除病理肿块并进行组织病理学检查后,诊断为混合型神经节神经母细胞瘤。这种肿瘤与神经母细胞瘤、神经节瘤和结节型神经节神经母细胞瘤一样,属于神经母细胞瘤性肿瘤(NTs),起源于交感神经系统的原始细胞。NTs相当罕见,但仍是儿童颅外实体瘤的主要类型,其症状通常在肿瘤性病变已经进展到相对较晚阶段时才出现。本综述的目的是介绍有关神经节神经母细胞瘤的当前信息,特别强调非特异性胃肠道症状作为该肿瘤的首发症状及其诊断方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de11/10531539/e46f9edec93d/jcm-12-06092-g001.jpg

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