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一例罕见的胰腺囊性神经内分泌肿瘤病例。

The rare case of a cystic pancreatic neuroendocrine tumor.

作者信息

Kumar Tarun, Gupta Brijnandan, Das Prasenjit, Madhusudhan Kumble S

机构信息

All India Institute of Medical Sciences, Department of Pathology. Patna, Bihar, India.

All India Institute of Medical Sciences, Department of Pathology. New Delhi, India.

出版信息

Autops Case Rep. 2020 Jun 5;10(3):e2020171. doi: 10.4322/acr.2020.171.

Abstract

The pancreatic neuroendocrine tumors (PanNETs) most commonly present as solid neoplasms; however, very rarely, they may present primarily as cystic neoplasms. Most of the cystic PanNETs are non-secreting tumors, and the radiological features are not well defined. Hence pre-operative diagnosis is usually challenging and the tumors are misdiagnosed as mucinous cystic neoplasms, intraductal papillary mucinous neoplasms, serous cystic neoplasms, solid pseudopapillary neoplasms, and non-neoplastic cysts. However, the management depends on the accurate diagnosis of these cystic lesions, which poses a dilemma. Herein, we report the case of a cystic PanNET in the tail of the pancreas, which was clinically and radiologically misdiagnosed as a mucinous cystic neoplasm. This case is reported to highlight this issue to the medical community regarding the diagnostic difficulty in such rare non-functioning pancreatic neuroendocrine tumors.

摘要

胰腺神经内分泌肿瘤(PanNETs)最常表现为实性肿瘤;然而,极为罕见的是,它们可能主要表现为囊性肿瘤。大多数囊性PanNETs是非分泌性肿瘤,其放射学特征并不明确。因此,术前诊断通常具有挑战性,这些肿瘤常被误诊为黏液性囊性肿瘤、导管内乳头状黏液性肿瘤、浆液性囊性肿瘤、实性假乳头状肿瘤和非肿瘤性囊肿。然而,治疗取决于对这些囊性病变的准确诊断,这就造成了两难局面。在此,我们报告一例胰腺尾部的囊性PanNET病例,该病例在临床和放射学上被误诊为黏液性囊性肿瘤。报告该病例是为了向医学界强调这种罕见的无功能性胰腺神经内分泌肿瘤的诊断困难问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dde/7703451/ac69081d4868/autopsy-10-3-e2020171-gf01.jpg

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