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胆囊神经内分泌肿瘤:1例罕见病例报告并文献复习

Neuroendocrine tumor of the gall bladder: A rare case report with review of literature.

作者信息

Marak James R, Kumar Tushant, Dwivedi Shivam, Khurana Rohini

机构信息

Department of Radiodiagnosis, Dr. RMLIMS, Lucknow, Uttar Pradesh, 226010, India.

Department of Radiation Oncology, Dr. RMLIMS, Lucknow, Uttar Pradesh, 226010, India.

出版信息

Radiol Case Rep. 2023 Aug 26;18(11):3912-3916. doi: 10.1016/j.radcr.2023.08.015. eCollection 2023 Nov.

Abstract

Neuroendocrine tumor of the gall bladder is an extremely rare malignancy, accounting for only 0.2% of all neuroendocrine tumors. Gall Bladder-Neuroendocrine Tumors (GB-NETs) are mainly diagnosed on histological examination of GB samples after cholecystectomy or after any biliary pathology surgery since it is very difficult to diagnose based on imaging. The overall outcome of gallbladder NET is worse than the adenocarcinoma of the gallbladder. No focused approach towards its treatment is available in literature due to its rarity. We share our experience of gall bladder NET in a 37-year-old female who was successfully managed at our institution.

摘要

胆囊神经内分泌肿瘤是一种极其罕见的恶性肿瘤,仅占所有神经内分泌肿瘤的0.2%。胆囊神经内分泌肿瘤(GB-NETs)主要在胆囊切除术后或任何胆道病理手术后对胆囊样本进行组织学检查时得以诊断,因为基于影像学很难做出诊断。胆囊神经内分泌肿瘤的总体预后比胆囊腺癌更差。由于其罕见性,文献中没有针对其治疗的专门方法。我们分享了一名37岁女性胆囊神经内分泌肿瘤患者在我们机构成功治疗的经验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff8e/10473970/35014c0a4f7e/gr1.jpg

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