Journal List > Korean J Gastroenterol > v.63(2) > 1007195

Park, Kim, Lim, Lee, Choi, Song, Lee, Jung, Kim, and Park: Endoscopic Resection as a Possible Radical Treatment for Duodenal Gangliocytic Paraganglioma: A Report of Four Cases

Abstract

Gangliocytic paraganglioma (GP) is a rare, benign tumor which is usually found in the duodenum. We here report four recent cases of GP, with successful endoscopic resection in three cases, including a lesion on the ampulla of Vater. In all cases, each lesion had a stalk that facilitated removal using an endoscopic approach. Endoscopic mucosal resection is a feasible and safe treatment if the location, depth, and lymph node status are all favorable and is also helpful for definite diagnosis of unknown duodenal mass. To avoid morbidity resulting from open surgical resection, careful inspection for the peduncle of the GP will help determine the feasibility of endoscopic resection.

References

1. Dahl EV, Waugh JM, Dahlin DC. Gastrointestinal ganglioneur-omas; brief review with report of a duodenal ganglioneuroma. Am J Pathol. 1957; 33:953–965.
2. Okubo Y, Wakayama M, Nemoto T, et al. Literature survey on epidemiology and pathology of gangliocytic paraganglioma. BMC Cancer. 2011; 11:187.
crossref
3. Wong A, Miller AR, Metter J, Thomas CR Jr. Locally advanced duodenal gangliocytic paraganglioma treated with adjuvant radiation therapy: case report and review of the literature. World J Surg Oncol. 2005; 3:15.
crossref
4. Barret M, Rahmi G, Duong van Huyen JP, Landi B, Cellier C, Berger A. Duodenal gangliocytic paraganglioma with lymph node metastasis and an 8-year follow-up: a case report. Eur J Gastroenterol Hepatol. 2012; 24:90–94.
5. Sundararajan V, Robinson-Smith TM, Lowy AM. Duodenal gangliocytic paraganglioma with lymph node metastasis: a case report and review of the literature. Arch Pathol Lab Med. 2003; 127:e139–e141.
crossref
6. Kwon J, Lee SE, Kang MJ, Jang JY, Kim SW. A case of gangliocytic paraganglioma in the ampulla of Vater. World J Surg Oncol. 2010; 8:42.
crossref
7. Plaza JA, Vitellas K, Marsh WL Jr. Duodenal gangliocytic paraganglioma: a radiological-pathological correlation. Ann Diagn Pathol. 2005; 9:143–147.
crossref
8. Nagai T, Torishima R, Nakashima H, et al. Duodenal gangliocytic paraganglioma treated with endoscopic hemostasis and resection. J Gastroenterol. 2004; 39:277–283.
crossref
9. Morita T, Tamura S, Yokoyama Y, et al. Endoscopic resection of a duodenal gangliocytic paraganglioma. Dig Dis Sci. 2007; 52:1400–1404.
crossref
10. El Idrissi-Lamghari A, Rioux-Leclercq N, Pagenault M, Bretagne JF. Voluminous juxtapapillary gangliocytic paraganglioma. Gastrointest Endosc. 2005; 62:445–446.
crossref
11. Witkiewicz A, Galler A, Yeo CJ, Gross SD. Gangliocytic paraganglioma: case report and review of the literature. J Gastrointest Surg. 2007; 11:1351–1354.
crossref

Fig. 1.
(A) Case 1. Endoscopic view of the duodenal tumor with an ulcerated surface and stalk. (B) Case 2. Huge duodenal mass with a large stalk. (C) Case 3. Duodenoscope side view showing a short stalk. (D) Case 4. Endoscopic view of the subepithelial tumor of the duodenum with a stalk.
kjg-63-114f1.tif
Fig. 2.
Photomicrographs showing key features of the gangliocytic paraganglioma in case 1 (H&E). (A) Epithelioid cell nests are located in the submucosal area (×40). (B) Epithelioid cells are arranged in nests or trabeculae (×100). (C) Epithelioid cells are large, polygonal or fusiform with an abundant eosinophilic granular cytoplasm (×400). (D) The ganglion cells (arrow) are scattered throughout (×400).
kjg-63-114f2.tif
Fig. 3.
Photomicrographs showing representative immunohistochemistry of the gangliocytic paraganglioma in case 1. (A) Epithelioid cells showed positive staining for synaptophysin (×200). (B) Epithelioid cells showed positive staining for CD56 (×200). (C) Epithelioid cells are negative for chromogranin (×200). (D) Spindle cells encompassing the epithelioid nests are highlighted by S-100 protein (×200).
kjg-63-114f3.tif
TOOLS
ORCID iDs

Jeong Hoon Lee
https://orcid.org/http://orcid.org/0000-0002-0778-7585

Similar articles