Clinicopathological Features of Neuroendocrine Tumors in Gastroenteropancreatic Tract: A Single Center Study

被引:2
作者
Rafique, Zubaria [1 ]
Qasim, Aafia [1 ]
Zafar, Asma [1 ]
Ali, Seemal [1 ]
Chughtai, Akhtar S. [1 ]
Atiq, Aribah [1 ]
机构
[1] Chughtai Inst Pathol, Histopathol, Lahore, Pakistan
关键词
clinicopathological features; grading; neuroendocrine tumors; mixed neuroendocrine-non-neuroendocrine neoplasms; gastroenteropancreatic neuroendocrine tumors;
D O I
10.7759/cureus.27384
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Gastroenteropancreatic neuroendocrine tumors (GEP-NETs) are a heterogeneous group of tumors with varying biological, functional, and clinical characteristics that develop from the gastroenteropancreatic tract's diffuse neuroendocrine system. The objective of this study is to determine the clinicopathological features of GEP-NETs at our facility. Methodology: A cross-sectional analysis of 87 biopsies and resection specimens from January 2020 to January 2022 was performed. The histopathological reports as well as patient's demographic and clinic pathological data were obtained. Two pathologists with a special interest in gastroenteropancreatic pathology blindly reviewed all cases. The tumor grade and stage were determined using the WHO classification (2019) and the AJCC TNM system (8th edition). The data were analyzed with SPSS version 22 (IBM Corp., Armonk, NY, USA). Results: Of the total 87 patients, 49 (56.3%) were male. The age range was 11 to 80 years, with a mean of 45.7 +/- 16.4 and the majority (56.3%) were under 50 years. The most frequent symptom was abdominal pain (55.2%). The most common site of GEP-NETs was the appendix (21.8%), followed by the ileum (18.4%), with the majority of tumors being non-functional (96.5%). Furthermore, neuroendocrine tumor (NET) grade 1 accounts for 62% of the total, followed by NET grade 2 (24.1%), neuroendocrine carcinoma (NET) grade 3 (10.3%), and mixed neuroendocrine-non-neuroendocrine neoplasms (MINENs) (3.5%). Synaptophysin was found to be positive in 83.9% cases while Chromogranin A was positive in 39.1%. A pathologic tumor (pT) stage was determined in 47 resection specimens in our study and the most common stage was pT3 (36.1%). Nodal metastasis was found in 25.5% of patients. Conclusions: According to our study, appendix and ileum were the most common GEP-NETs sites. The tumor site and grade were shown to significantly correlate among the clinicopathological features but there was no discernible correlation between the tumor grade and the gender, age, or pathological tumor (pT) stage.
引用
收藏
页数:8
相关论文
共 50 条
[31]   Hereditary neuroendocrine tumors of the gastroenteropancreatic system [J].
Anlauf, Martin ;
Garbrecht, Nele ;
Bauersfeld, Juliane ;
Schmitt, Anja ;
Henopp, Tobias ;
Komminoth, Paul ;
Heitz, Philipp U. ;
Perren, Aurel ;
Kloeppel, Guenter .
VIRCHOWS ARCHIV, 2007, 451 :S29-S38
[32]   Clinicopathological Features and Prognosis of 35 Patients with Gastric Neuroendocrine Carcinomas: A Single-Center Experience [J].
Jiaqi, H. .
NEUROENDOCRINOLOGY, 2017, 105 :80-80
[33]   Clinicopathological features and surgical outcomes of neuroendocrine tumors of ampulla of Vater [J].
Yang, Kwangho ;
Yun, Sung Pil ;
Kim, Suk ;
Shin, Nari ;
Park, Do Youn ;
Seo, Hyung Il .
BMC GASTROENTEROLOGY, 2017, 17
[34]   Novel Agents in Gastroenteropancreatic Neuroendocrine Tumors [J].
Stevenson, Ryan ;
Libutti, Steven K. ;
Saif, Muhammad Wasif .
JOURNAL OF THE PANCREAS, 2013, 14 (02) :152-154
[35]   Update in the management of gastroenteropancreatic neuroendocrine tumors [J].
Sedlack, Andrew J. H. ;
Varghese, Diana Grace ;
Naimian, Amirkia ;
Anari, Pouria Yazdian ;
Bodei, Lisa ;
Hallet, Julie ;
Riechelmann, Rachel P. ;
Halfdanarson, Thor ;
Capdevilla, Jaume ;
Del Rivero, Jaydira .
CANCER, 2024, 130 (18) :3090-3105
[36]   Gastroenteropancreatic neuroendocrine tumors: Role of surgery [J].
Sauvanet, Alain .
ANNALES D ENDOCRINOLOGIE, 2019, 80 (03) :175-181
[37]   Hereditary neuroendocrine tumors of the gastroenteropancreatic system [J].
Martin Anlauf ;
Nele Garbrecht ;
Juliane Bauersfeld ;
Anja Schmitt ;
Tobias Henopp ;
Paul Komminoth ;
Philipp U. Heitz ;
Aurel Perren ;
Günter Klöppel .
Virchows Archiv, 2007, 451 :29-38
[38]   The role of endoscopy in gastroenteropancreatic neuroendocrine tumors [J].
Magno, L. ;
Sivero, L. ;
Napolitano, V. ;
Ruggiero, S. ;
Fontanarosa, G. ;
Massa, S. .
GIORNALE DI CHIRURGIA, 2010, 31 (6-7) :341-343
[39]   Octreotide and Lanreotide in Gastroenteropancreatic Neuroendocrine Tumors [J].
Venkata K. Pokuri ;
Mei Ka Fong ;
Renuka Iyer .
Current Oncology Reports, 2016, 18
[40]   Neuroendocrine Gastroenteropancreatic Tumors: Where Are We? [J].
Ulla Rocha, Jose L. ;
Salgado, Angel ;
Sardina Ferreiro, Raquel ;
Fernandez Catalina, Pablo ;
Gallardo, Elena .
SURGICAL LAPAROSCOPY ENDOSCOPY & PERCUTANEOUS TECHNIQUES, 2017, 27 (01) :36-41