Duodenal gangliocytic paraganglioma with lymph node metastases: a case report and comparative review of 31 cases

被引:15
|
作者
Cathcart, Sahara J. [1 ]
Sasson, Aaron R. [2 ]
Kozel, Jessica A. [3 ]
Oliveto, Jennifer M. [4 ]
Ly, Quan P. [5 ]
机构
[1] Dept Pathol & Microbiol, 985900 Nebraska Med Ctr, Omaha, NE 68198 USA
[2] Stony Brook Med, Dept Surg, Div Surg Oncol, Stony Brook, NY 11794 USA
[3] Midwest Pathol Associates LLC, Overland Pk, KS 66210 USA
[4] Univ Nebraska Med Ctr, Dept Radiol, Omaha, NE 68198 USA
[5] Univ Nebraska Med Ctr, Dept Surg, Div Surg Oncol, Omaha, NE 68198 USA
关键词
Gangliocytic paraganglioma; Metastases; Duodenum; Lymph node dissection; Pancreaticoduodenectomy; OF-THE-LITERATURE; MALIGNANT PARAGANGLIOMA; AMPULLA; VATER; FEATURES; LIVER;
D O I
10.12998/wjcc.v5.i6.222
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Gangliocytic paraganglioma (GP) is a rare tumor of uncertain origin most often located in the second portion of the duodenum. It is composed of three cellular components: Epithelioid endocrine cells, spindlelike/sustentacular cells, and ganglion-like cells. While this tumor most often behaves in a benign manner, cases with metastasis are reported. We describe the case of a 62-year-old male with a periampullary GP with metastases to two regional lymph nodes who was successfully treated with pancreaticoduodenectomy. Using PubMed, EMBASE, EBSCOhost MEDLINE and CINAHL, and Google Scholar, we searched the literature for cases of GP with regional lymph node metastasis and evaluated the varying presentations, diagnostic workup, and disease management of identified cases. Thirty-one cases of GP with metastasis were compiled (30 with at least lymph node metastases and one with only distant metastasis to bone), with age at diagnosis ranging from 16 to 74 years. Ratio of males to females was 19: 12. The most common presenting symptoms were abdominal pain (55%) and gastrointestinal bleeding or sequelae (42%). Twenty-five patients underwent pancreaticoduodenectomy. Five patients were treated with local resection alone. One patient died secondary to metastatic disease, and one died secondary to perioperative decompensation. The remainder did well, with no evidence of disease at follow-up from the most recent procedure (except two in which residual disease was deliberately left behind). Of the 26 cases with sufficient histological description, 16 described a primary tumor that infiltrated deep to the submucosa, and 3 described lymphovascular invasion. Of the specific immunohistochemistry staining patterns studied, synaptophysin (SYN) stained all epithelioid endocrine cells (18/18). Neuron specific enolase (NSE) and SYN stained most ganglion-like cells (7/8 and 13/18 respectively), and S-100 stained all spindle-like/sustentacular cells (21/21). Our literature review of published cases of GP with lymph node metastasis underscores the excellent prognosis of GP regardless of specific treatment modality. We question the necessity of aggressive surgical intervention in select patients, and argue that local resection of the mass and metastasis may be adequate. We also emphasize the importance of pre-surgical assessment with imaging studies, as well as post-surgical follow-up surveillance for disease recurrence.
引用
收藏
页码:222 / 233
页数:12
相关论文
共 50 条
  • [41] Fine-needle aspiration biopsy of duodenal gangliocytic paraganglioma: Report of two cases
    Patel, Nilesh P.
    Conway, Jason D.
    Cappellari, James O.
    Gibson, Kathleen G.
    AMERICAN JOURNAL OF GASTROENTEROLOGY, 2007, 102 : S207 - S208
  • [42] DUODENAL GANGLIOCYTIC PARAGANGLIOMA - CLINICOPATHOLOGICAL AND IMMUNOCYTOCHEMICAL STUDY OF 11 CASES
    SCHEITHAUER, BW
    NORA, FE
    LECHAGO, J
    WICK, MR
    CRAWFORD, BG
    WEILAND, LH
    CARNEY, JA
    AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 1986, 86 (05) : 559 - 565
  • [43] A Rare Case of Duodenal Gangliocytic Paraganglioma Treated With Ampullectomy
    Elghezewi, Abdelwahap
    Hammad, Mohamed
    Kota, Dheeraja
    Mohamed, Mujtaba
    Pantangi, Pramod
    AMERICAN JOURNAL OF GASTROENTEROLOGY, 2023, 118 (10): : S2499 - S2499
  • [44] GANGLIOCYTIC PARAGANGLIOMA ASSOCIATED WITH DUODENAL ADENOCARCINOMA - CASE-REPORT WITH IMMUNOHISTOCHEMICAL EVALUATION
    ANDERS, KH
    GLASGOW, BJ
    LEWIN, KJ
    ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE, 1987, 111 (01) : 49 - 52
  • [45] Duodenal gangliocytic paraganglioma: A very rare cause for upper gastrointestinal bleeding: Case report with review of literature
    Arif, Sardar Hassan
    Mohammed, Ayad Ahmad
    Yaqo, Rafil T.
    INTERNATIONAL JOURNAL OF SURGERY CASE REPORTS, 2020, 75 : 408 - 412
  • [46] Gangliocytic paraganglioma: a rare case with metastases of all 3 elements to liver and lymph nodes
    Rowsell, Corwyn
    Coburn, Natalie
    Chetty, Runjan
    ANNALS OF DIAGNOSTIC PATHOLOGY, 2011, 15 (06) : 467 - 471
  • [47] An unusual case of duodenal obstruction-gangliocytic paraganglioma
    Mann, C. M.
    Bramhall, S. R.
    Buckels, J. A.
    Taniere, P.
    JOURNAL OF HEPATO-BILIARY-PANCREATIC SURGERY, 2009, 16 (04): : 562 - 565
  • [48] A rare case of ampullary gangliocytic paraganglioma with lymph node metastasis: histological and immunohistochemical analysis
    Ben Makhlouf, W.
    Zehani, A.
    Ayari, A.
    Khadhar, A.
    Chelly, I.
    Azouz, H.
    Bellil, K.
    Haouet, S.
    VIRCHOWS ARCHIV, 2024, 485 : S471 - S471
  • [49] Gangliocytic paraganglioma of the duodenum:a case report
    WU Guo-cong
    WANG Kang-li
    ZHANG Zhong-tao
    中华医学杂志(英文版), 2012, (02) : 388 - 389
  • [50] Gangliocytic paraganglioma of the duodenum: A case report
    Akpinar, Eda
    Kaygusuz, Gulsah
    Germen, Hatice
    Erden, Esra
    Cansiz, Cevriye
    VIRCHOWS ARCHIV, 2007, 451 (02) : 332 - 332