Nisan 2012 / (20 - 1)
Gastrik nöroendokrin tümörün keple mukozektomi yapılarak çıkarılması
Yazarlar
Meltem ERGÜN1, Fatih Oğuz ÖNDER1, Nesrin TURHAN2, Ertuğrul KAYAÇETİN1
Kurumlar
Departments of 1Gastroenterology and 2Pathology, Yüksek İhtisas Education and Training Hospital, Ankara
Özet
Midenin nöroendokrin tümörleri nadirdir, ancak sıklığı giderek artmaktadır. Önceleri cerrahi rezeksiyon tedavi seçenekleri arasında ön plandayken özellikle 2 cm?den küçük tümörlerde endoskopik mukozal rezeksiyon rutin tedavi seçeneği haline gelmiştir. Biz keple mukozektomi yapılarak tedavi edilen bir olguyu sunuyoruz.
Anahtar Kelimeler
Mukozektomi, nöroendokrin tümör, endoskopik rezek siyon
Giriş
Neuroendocrine tumors (NETs) are a heterogeneous group of
rare cancers that derive from neuroendocrine cells and show
distinct functional and biological behavior depending on the
location, tumor size, and clinical symptoms (1).
NETs are classified histologically based on tumor differentiation. In general, neuroendocrine neoplasms are divided into
well-differentiated and poorly differentiated categories. According to the World Health Organization (WHO) 2010 classification, there are three types of NETs: well-differentiated
grade 1 (<2 mitoses / 10 high-power fields (hpf) AND <3%
Ki67 index), intermediate-differentiated grade 2 (2-20 mitoses / 10 hpf OR 3%-20% Ki67 index) and poorly differentiated grade 3 neuroendocrine cancer (>20 mitoses / 10 hpf OR
>20% Ki67 index) (2).
Carcinoid tumors are the most common NETs. Three types of
gastric carcinoid tumors are described. Type I: associated
with chronic atrophic gastritis, Type II: associated with Zollinger-Ellison syndrome, and Type III sporadic lesions. Gastric carcinoids associated with hypergastrinemia are relatively
benign, and endoscopic resection is a feasible treatment modality for lesions that are 2 cm or smaller (3).
Olgu
Standard treatment for NETs is surgical resection. Endoscopic
treatment is an accepted treatment modality for small (≤ 20
mm) submucosal lesions. It has been proven that the small lesion limited in the submucosa with intact muscularis propria has a minimal risk for metastatic disease (4). Conventional
snare excision, cap-assisted mucosectomy, submucosal dissection, and unroofing techniques may be preferred depending on the type and size of the lesion (5,6). Cap-assisted endoscopic resection technique is a valid, safe, effective treatment, and it allows total excision of the lesion; therefore, full
pathologic assessment is possible to determine the malignant
potential.
Tartışma
Standard treatment for NETs is surgical resection. Endoscopic
treatment is an accepted treatment modality for small (≤ 20
mm) submucosal lesions. It has been proven that the small lesion limited in the submucosa with intact muscularis propria has a minimal risk for metastatic disease (4). Conventional
snare excision, cap-assisted mucosectomy, submucosal dissection, and unroofing techniques may be preferred depending on the type and size of the lesion (5,6). Cap-assisted endoscopic resection technique is a valid, safe, effective treatment, and it allows total excision of the lesion; therefore, full
pathologic assessment is possible to determine the malignant
potential.
Kaynaklar
1. Klimstra DS, Modlin IR, Coppola D, et al. The pathologic classification
of neuroendocrine tumors: a review of nomenclature, grading, and staging systems. Pancreas 2010;39:707-12. Review.
2. Bosman F, Carneiro F, Hruban R, et al., eds. WHO Classification of Tumours of the Digestive System. Lyon, France: IARC Press, 2010.
3. Scherübl H, Jensen RT, Cadiot G, et al. Management of early gastrointestinal neuroendocrine neoplasms. World J Gastrointest Endosc 2011;
3:133-9.
4. Ruszniewski P, Delle Fave G, Cadiot G, et al. Well-differentiated gastric
tumors/carcinomas. Neuroendocrinology 2006;84:158-64.
5. Lee CK, Chung IK, Lee SH, et al. Endoscopic partial resection with the
unroofing technique for reliable tissue diagnosis of upper GI subepithelial tumors originating from the muscularis propria on EUS. Gastrointest
Endosc 2010;71:188-94.
6. Kim BS, Oh ST, Yook JH, et al. Typical carcinoids and neuroendocrine
carcinomas of the stomach: differing clinical courses and prognoses. Am
J Surg 2010;200:328-33.