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100,000), 1,2,3 includes tumors arising from the GI tract (GNET) and Pancreas (PNET). Within the GI tract, these are found commonly in small bowel and appendix, followed by rectum and stomach 4 . Duodenal occurrence of NETs is very rare and represents only 2-3% of all NETs. 4,5 Most of these tumors are small, submucosal masses 5,6 and are divided into five types: duodenal gastrinomas, duodenal somatostatinomas, nonfunctioning NETs, ganglioytic paragangliomas, and poorly differentiated NE carcinomas. They may occur sporadically or in association with Multiple Endocrine Neoplasia (MEN-1) and Zollinger-Ellison Syndrome (ZES). The tumor seen in our patient was a nonfunctioning NET. Although the old term carcinoid sounds benign, these tumors are capable of local and distant metastasis. The most common presentation is abdominal pain, but presentation may vary from nonspecific dyspepsia to GI bleeding. 5,6 Given the indolent and slow-growing nature of these tumors, NETs may remain asymptomatic until they grow large or may be incidentally discovered on imaging or endoscopy. In our case, patient had intractable nausea, likely due to intermittent, low-grade outlet obstruction from the tumor growing in duodenal wall. Routine imaging, including CT and MRI, can detect large-sized NETs and also metastases but fails to reliably detect smaller submucosal lesions. 7 In such scenarios, EUS is the most useful diagnostic modality to detect accurately the tissue of origin, as in our patient, which may be difficult at times with conventional imaging. EUS serves well in defining the size of tumor, level of invasion, histology by FNA, and regional lymph-node metastasis. 4,7,8 Additionally, serum chromogranin levels are seen elevated in 80% of the tumors. 9 In addition to cross-sectional imaging and EUS, somatostatin » » This is a very uncommon presentation, but teaches endoscopists to investigate thoughtfully such purportedly trivial complaints to unravel unexpected findings, like NETs. » » EUS is an irreplaceable asset in investigation of submucosal masses and can help differentiate the tissue of origin even in cases where cross- sectional imaging fails. References Image 4: CD56 immunohistochemical stain showing diffuse membranous positivity of tumor cells. scintigraphy (SRS) is valuable in identifying small, metastatic lesions, owing to the increased expression of somatostatin receptors by these tumors. 10,11 Histologically, NETs stain positive for pan-sensitive neuroendocrine markers, including Chromogranin A, synaptophysin, and neuron- specific enolase. 10 Moreover, Ki-67 level, which measures the proliferative capacity of the tumor cells, is measured to grade the tumors according to the WHO classification, which determines the overall prognosis. 12 If the Ki-67 index is <2%, tumors are graded into G1, 2-20% into grade 2, and >20% into G3. Management of NETs depends on size and grade of tumor and extent of metastasis. Small, submucosal tumors of < 1cm without any regional lymph node involvement can be safely removed by endoscopic resection. For larger tumors, full thickness excision is needed either by laparoscopy or laparotomy. Alternative therapy (medical) is considered for non-resectable, metastatic tumors or high-risk surgical candidates, which may include somatostatin analogues, interferon, and chemotherapy, 13,14 (all evolving fields). Radiation therapy (external beam radiotherapy; EBRT) may be considered for palliative purposes and is suitable for patients with increased uptake of specific radionucleotide agents (like I-MIBG). Additional modalities, including radiofrequency ablation or hepatic artery embolization, may be needed for management of non-resectable hepatic metastatic lesions and for symptomatic control of functional NETs. Learning points Image 3: Synaptophysin immunohistochemical stain showing diffuse positive cytoplasmic and membranous staining of tumor cells. » » Duodenal NETs are rare, slow growing, and may have insidious presentation, like our patient with nausea, which was likely due to intermittent, low-grade-outlet obstruction. 1. Rehfeld JF. The new biology of gastrointestinal hormones. Physiol Rev 1998; 78: 1087–108 2. Pearse AG. The cytochemistry and ultrastructure of polypeptide hormone-producing cells of the APUD series and the embryologic, physiologic and pathologic implications of the concept.
J Histochem Cytochem 1969; 17: 303–13. 3. Oberndorfer S. Karzinoide Tumoren des Dünndarms.
Frankf Z Pathol 1907; 1: 426–32. 4. Modlin IM, Lye KD, Kidd M. A 5-decade analysis of 13 715; carcinoid tumors. Cancer 2003; 97: 934–59. 5. Stridsberg M, Oberg K, Li Q, et al. Measurement of
chromogranin A, chromogranin B (secretogranin I), chromogranin C (secretogranin II) and pancreastatin in plasma and urine from patients with carcinoid tumours and endocrine pancreatic tumours. J Endocrinol 1995; 144: 49–59. 6. Modlin IM, Kidd M, Latich I, et al. Current status of gastrointestinal carcinoids. Gastroenterology 2005; 128: 1717–51. 7. Tonnies H, Toliat MR, Ramel C, et al. Analysis of sporadic neuroendocrine tumours of the enteropancreatic system by comparative genomic hybridisation. Gut 2001; 48: 536–41. 8. Thakker RV. Multiple endocrine neoplasia type 1. In: DeGroot LJ, Jamesson JL, eds. Endocrinology, 5th edn. Philadelphia, USA: Elsevier Saunders, 2006: 3509–21. 9. Lollgen RM, Hessman O, Szabo E, et al. Chromosome 18 deletions are common events in classical midgut carcinoid tumors.
Int J Cancer 2001; 92: 812–15. 10. DeLellis RA, Lloyd RV, Heitz PU, Eng C, eds. World Health Organization classification of tumours, pathology and genetics of tumours of endocrine organs. Lyon: IARC Press, 2004. Contact AMS for a complete list of references. NUMBER 3 SEPTEMBER 2019 • 59