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小肠同步性肿瘤:一项诊断挑战。

Synchronous Neoplasms of the Small Bowel: A Diagnostic Challenge.

作者信息

de Sousa Miranda Inês, Ávila Leonor, Castro Luís, Rocha Sara, Monteiro Marta, Domingos Raquel

机构信息

Internal Medicine Department, Hospital Egas Moniz, Centro Hospitalar Lisboa Ocidental, Lisbon, Portugal.

General Surgery Department, Hospital Egas Moniz, Centro Hospitalar Lisboa Ocidental, Lisbon, Portugal.

出版信息

Eur J Case Rep Intern Med. 2022 Mar 14;9(3):003231. doi: 10.12890/2022_003231. eCollection 2022.

Abstract

UNLABELLED

Small bowel tumours are rare, representing about 0.5% of all tumours and about 3% of gastrointestinal tract tumours. The low prevalence contrasts with the vast surface area of the small intestine, which accounts for over 90% of the surface area of the digestive tract. The frequency of small tumours decreases from proximal to distal, and therefore from the duodenum to the ileum. The histological types differ in terms of prevalence according to the affected segment, with adenocarcinoma being the most frequent in the duodenum and jejunum and carcinoid tumour in the ileum. Diagnosis is challenging due to clinical non-specificity, low prevalence and a low level of suspicion. Schwannomas are typically benign tumours that arise from Schwann's cells and are rarely found in the small intestine. It is even more rare to find them together with another histological type, namely adenocarcinoma. No cases have been reported in the literature of these lesions occurring in the small intestine simultaneously. Further studies are needed to clarify the underlying pathophysiology of these synchronous tumours. The authors present the case of an 86-year-old female patient admitted for high intestinal subocclusion, with refractory vomiting and involuntary weight loss. Two synchronous lesions in the digestive tract were identified: an adenocarcinoma in the duodenum and a schwannoma in the ileum. The patient underwent surgical resection of both lesions. A high level of suspicion combined with a multidisciplinary approach is necessary for timely diagnosis and surgical resolution.

LEARNING POINTS

Small bowel neoplasms are rare and clinically non-specific; in addition, diagnosis is difficult due to imaging artifacts and tumour inaccessibility for biopsy for definitive histological diagnosis.Gastrointestinal schwannomas are rare and the pathophysiology of synchrony with other histological subtypes remains to be clarified.A multidisciplinary approach from the beginning is important for a timely diagnosis and better outcome.

摘要

未标注

小肠肿瘤很罕见,约占所有肿瘤的0.5%,占胃肠道肿瘤的约3%。这种低发病率与小肠巨大的表面积形成对比,小肠表面积占消化道表面积的90%以上。小肠肿瘤的发病率从近端到远端逐渐降低,即从十二指肠到回肠逐渐降低。根据受累节段不同,组织学类型的发病率也有所不同,腺癌在十二指肠和空肠中最为常见,类癌肿瘤在回肠中最为常见。由于临床症状不具特异性、发病率低且怀疑程度低,诊断具有挑战性。神经鞘瘤通常是起源于施万细胞的良性肿瘤,在小肠中很少见。更罕见的是它们与另一种组织学类型,即腺癌同时出现。文献中尚未报道这些病变在小肠中同时发生的病例。需要进一步研究以阐明这些同步性肿瘤的潜在病理生理学。作者报告了一例86岁女性患者,因高位小肠梗阻入院,伴有顽固性呕吐和非自愿体重减轻。在消化道中发现了两个同步病变:十二指肠腺癌和回肠神经鞘瘤。患者接受了两个病变的手术切除。高度怀疑并结合多学科方法对于及时诊断和手术解决是必要的。

学习要点

小肠肿瘤罕见且临床症状不具特异性;此外,由于成像伪影和肿瘤难以获取活检进行明确的组织学诊断,诊断困难。胃肠道神经鞘瘤罕见,与其他组织学亚型同步发生的病理生理学仍有待阐明。从一开始就采用多学科方法对于及时诊断和获得更好的结果很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e649/8988503/6d25fe599a86/3231_Fig1.jpg

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