Pankreasın Endokrin Hastalıklarında Cerrahi Yaklaşımlar

Yazarlar

Emre Tunç

Özet

Pankreas nöroendokrin tümörleri (pNET), insülinoma ve gastrinoma gibi fonksiyonel veya nonfonksiyonel tümörlerden oluşan heterojen bir gruptur ve tüm pankreas tümörlerinin %1-2'sini kapsar. Tanıda klinik semptomlar, biyokimyasal analizler ile ultrasonografi, BT, MR ve EUS gibi kesitsel görüntüleme yöntemleri kritik rol oynar. pNET'lerin tedavisinde cerrahi yaklaşım; tümörün fonksiyonel durumuna, boyutuna, lokalizasyonuna ve MEN-1 sendromuyla ilişkisine göre kişiselleştirilir. 2 cm'den küçük, ana pankreas kanalına uzak sporadik insülinomalarda enükleasyon parankim koruyucu bir seçenekken; gastrinoma, glukagonoma ve malignite riski yüksek diğer tümörlerde veya ana kanala yakın yerleşimlerde standart radikal rezeksiyonlar (distal pankreatektomi, pankreatikoduodenektomi) ve lenfadenektomi uygulanır. Karaciğer metastazlarında cerrahi rezeksiyon G1-G2 tümörlerde önerilir. Son dekatta laparoskopik ve robotik gibi minimal invaziv cerrahi yaklaşımlar, açık cerrahiye kıyasla daha az kan kaybı ve hızlı iyileşme avantajlarıyla öne çıkmaktadır. Postoperatif takip, nüks riski nedeniyle fonksiyonel tümörlerde ilk 3 yıl 6-12 ayda bir, nonfonksiyonel olanlarda ise daha sık aralıklarla kesitsel görüntüleme ve hormon panelleriyle yaşam boyu sürdürülmelidir.

Pancreatic neuroendocrine tumors (pNETs) are a heterogeneous group of functional tumors, such as insulinomas and gastrinomas, and nonfunctional tumors, accounting for 1-2% of all pancreatic neoplasms. Diagnosis relies heavily on clinical symptoms, biochemical analyses, and cross-sectional imaging modalities including ultrasound, CT, MRI, and EUS. Surgical management of pNETs is highly customized based on tumor functionality, size, localization, and association with MEN-1 syndrome. Parenchymal-sparing enucleation is preferred for sporadic insulinomas smaller than 2 cm located away from the main pancreatic duct, whereas standard radical resections (distal pancreatectomy, pancreaticoduodenectomy) combined with lymphadenectomy are performed for gastrinomas, glucagononmas, large nonfunctional tumors, or lesions close to the main duct. Surgical resection is recommended for liver metastases in G1-G2 tumors. Over the past decade, minimally invasive surgical approaches, including laparoscopic and robotic surgery, have gained prominence due to advantages like reduced intraoperative blood loss and shorter hospital stays compared to open surgery. Postoperative lifelong follow-up is essential using cross-sectional imaging and hormonal evaluations, scheduled every 6-12 months for functional tumors and 3-6 months for nonfunctional tumors during the first three years.

Referanslar

Dasari A, Shen C, Halperin D, et al. Trends in the Incidence, Prevalence, and Survival Outcomes in Patients With Neuroendocrine Tumors in the United States. JAMA oncology. 2017;3(10): 1335–1342. doi:10.1001/jamaoncol.2017.0589

Hallet J, Law CHL, Cukier M, et al. Exploring the rising incidence of neuroendocrine tumors: a population-based analysis of epidemiology, metastatic presentation, and outcomes. Cancer. United States; 2015;121(4): 589–597. doi:10.1002/cncr.29099

Kapan M. 2015 Pankreas Nöroendokrin Tümörleri. 25–33. Ankara

Bouquot M, Gaujoux S, Cauchy F, et al. Pancreatectomy for pancreatic incidentaloma: What are the risks? Pancreatology : official journal of the International Association of Pancreatology (IAP) . [et al.]. Switzerland; 2018;18(1): 114–121. doi:10.1016/j.pan.2017.11.002

Hofland J, Zandee WT, de Herder WW. Role of biomarker tests for diagnosis of neuroendocrine tumours. Nature reviews. Endocrinology. England; 2018;14(11): 656–669. doi:10.1038/s41574-018-0082-5

Dushyant V. S, Abdominal Imagining . Second edition. Elsevier

Vanderveen K, Grant C. Insulinoma. Cancer treatment and research. United States; 2010;153: 235–252. doi:10.1007/978-1-4419-0857-5_13

Mehrabi A, Fischer L, Hafezi M, et al. A systematic review of localization, surgical treatment options, and outcome of insulinoma. Pancreas. United States; 2014;43(5): 675–686. doi:10.1097/MPA.0000000000000110

Ito T, Masui T, Komoto I, et al. JNETS clinical practice guidelines for gastroenteropancreatic neuroendocrine neoplasms: diagnosis, treatment, and follow-up: a synopsis. Journal of gastroenterology. 2021;56(11): 1033–1044. doi:10.1007/s00535-021-01827-7

The Guidelines Committee of the Japan Neuroendocrine Tumor Society.The Clinical Guidelines for Gastroenteropancreatic Neuroendocrine Tumors in Japan (in Japanese). 2015; http://jnets.umin.jp/pdf/guideline001s.pdf

Zhao Y-P, Zhan H-X, Zhang T-P, et al. Surgical management of patients with insulinomas: Result of 292 cases in a single institution. Journal of surgical oncology. United States; 2011;103(2): 169–174. doi:10.1002/jso.21773

Abbasoğlu O. 2019. Pankreasın Nöroendokrin Neoplazileri Osman Abbasoğlu (ed) Karaciğer, Safra Yolları ve Pankreas Cerrahisi (301-310). Ankara. Dünya Tıp Kitapevi

Towsend C.M, Beauchamp R.D, Evers B.M et al. Sabiston Textbook of Surgery,20th Ed Elsevier.2017.

Souche R, Hobeika C, Hain E, et al. Surgical Management of Neuroendocrine Tumours of the Pancreas. Journal of clinical medicine. 2020;9(9). doi:10.3390/jcm9092993

Jeune F, Taibi A, Gaujoux S. Update on the Surgical Treatment of Pancreatic Neuroendocrine Tumors. Scandinavian journal of surgery : SJS : official organ for the Finnish Surgical Society and the Scandinavian Surgical Society. England; 2020;109(1): 42–52. doi:10.1177/1457496919900417

de Rooij T, van Hilst J, Vogel JA, et al. Minimally invasive versus open distal pancreatectomy (LEOPARD): study protocol for a randomized controlled trial. Trials. 2017;18(1): 166. doi:10.1186/s13063-017-1892-9

Souche R, Herrero A, Bourel G, et al. Robotic versus laparoscopic distal pancreatectomy: a French prospective single-center experience and cost-effectiveness analysis. Surgical endoscopy. Germany; 2018;32(8): 3562–3569. doi:10.1007/s00464-018-6080-9

Partelli S, Bartsch DK, Capdevila J, et al. ENETS Consensus Guidelines for Standard of Care in Neuroendocrine Tumours: Surgery for Small Intestinal and Pancreatic Neuroendocrine Tumours. Neuroendocrinology. Switzerland; 2017;105(3): 255–265. doi:10.1159/000464292

Gelecek

25 Mayıs 2022

Lisans

Lisans