Primitive Neuroectodermal Tumor of the Pancreas

被引：25

作者：

Doi, Hirokazu ^{[1
]}

Ichikawa, Soichi ^{[1
]}

Hiraoka, Atsushi ^{[1
]}

Ichiryu, Misa ^{[1
]}

Nakahara, Hiromasa ^{[1
]}

Ochi, Hironori ^{[1
]}

Tanabe, Atsushi ^{[1
]}

Kodama, Akihiro ^{[1
]}

Hasebe, Aki ^{[1
]}

Miyamoto, Yasunao ^{[1
]}

Ninomiya, Tomoyuki ^{[1
]}

Horiike, Norio ^{[1
]}

Takamura, Kazuhito ^{[2
]}

Kawasaki, Hideki ^{[2
]}

Kameoka, Chieko ^{[3
]}

Kan, Miki ^{[3
]}

Doi, Shigekazu ^{[3
]}

Soga, Yoshiko ^{[3
]}

Tamura, Hiromi ^{[3
]}

Maeda, Toshiharu ^{[3
]}

Asaki, Akinori ^{[4
]}

Seno, Seijin ^{[4
]}

Iguchi, Haruo ^{[4
]}

Hasegawa, Tadashi ^{[5
]}

机构：

[1] Ehime Prefectural Cent Hosp, Dept Gastroenterol, Matsuyama, Ehime, Japan

[2] Ehime Prefectural Cent Hosp, Dept Surg, Matsuyama, Ehime, Japan

[3] Ehime Prefectural Cent Hosp, Dept Lab Med, Matsuyama, Ehime, Japan

[4] Natl Hosp Org, Shikoku Canc Ctr, Dept Gastroenterol, Matsuyama, Ehime, Japan

[5] Sapporo Med Univ, Sch Med, Dept Surg Pathol, Sapporo, Hokkaido, Japan

来源：

INTERNAL MEDICINE | 2009年 / 48卷 / 05期

关键词：

primitive neuroectodermal tumor; pancreas; FDG-PET; EWINGS-SARCOMA; EWS;

D O I：

10.2169/internalmedicine.48.1484

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

The primitive neuroectodermal tumor (PNET) of the pancreas, a member of Ewing's sarcoma family of tumors, is extremely rare. We treated a 37-year-old Japanese man who had a solitary pancreatic tumor 40 mm in diameter and multiple hepatic tumors with surgical resection. The PNET was positive for CD99 on immunohistochemical staining. Fluorescence in situ hybridization (FISH) was also performed, which revealed a Ewing sarcoma breakpoint region 1 (EWSR1) 22q12 rearrangement. According to the Japan-Ewing protocol, chemotherapy with Ifomide (ifosfamide), etoposide, vincristine, and cyclophosphamide was given after surgery. To the best of our knowledge, to date 13 PNET cases have been reported with a mean age for all patients of 19.3 years old. Surgical resection was performed in most cases and some patients received postoperative chemotherapy. The clinicopathologic characteristics and management of this extremely rare disease are also discussed.

引用

页码：329 / 333

页数：5

共 19 条

[1] Primitive neuroectodermal tumor of the pancreas -: An extremely rare tumor -: Case report and review of the literature [J].

Bülchmann, G ;

Schuster, T ;

Haas, RJ ;

Joppich, I .

KLINISCHE PADIATRIE, 2000, 212 (04) :185-188

[2] Molecular biology of the Ewing's sarcoma/primitive neuroectodermal tumor family [J].

de Alava, E ;

Gerald, WL .

JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (01) :204-213

[3]

Györke T, 2006, NUCL MED COMMUN, V27, P17

[4] PANCREATIC ENDOCRINE TUMORS - IMMUNO-CYTOCHEMICAL ANALYSIS OF 125 TUMORS [J].

HEITZ, PU ;

KASPER, M ;

POLAK, JM ;

KLOPPEL, G .

HUMAN PATHOLOGY, 1982, 13 (03) :263-271

[5]

LANDANYI A, 2000, HUM PATHOL, V31, P532

[6]

Luttges J, 1997, PATHOLOGE, V18, P233, DOI 10.1007/s002920050211

[7] Primitive neuroectodermal tumors of the pancreas - A report of seven cases of a rare neoplasm [J].

Movahedi-Lankarani, S ;

Hruban, RH ;

Westra, WH ;

Klimstra, DS .

AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2002, 26 (08) :1040-1047

[8] Localized Ewing tumor of bone:: Final results of the cooperative Ewing's Sarcoma Study CESS 86 [J].

Paulussen, M ;

Ahrens, S ;

Dunst, J ;

Winkelmann, W ;

Exner, GU ;

Kotz, R ;

Amann, G ;

Dockhorn-Dworniczak, B ;

Harms, D ;

Müller-Weihrich, S ;

Welte, K ;

Kornhuber, B ;

Janka-Schaub, G ;

Göbel, U ;

Treuner, J ;

Voûte, PA ;

Zoubek, A ;

Gadner, H ;

Jürgens, H .

JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (06) :1818-1829

[9] Primitive neuroectodermal tumor of the pancreas - A case report of an extremely rare tumor [J].

Perek, S ;

Perek, A ;

Sarman, K ;

Tuzun, H ;

Buyukunal, E .

PANCREATOLOGY, 2003, 3 (04) :352-356

[10] IMMUNOCYTOCHEMICAL STUDY OF 12E7 IN SMALL ROUND-CELL TUMORS OF CHILDHOOD - AN ASSESSMENT OF ITS SENSITIVITY AND SPECIFICITY [J].

RAMANI, P ;

RAMPLING, D ;

LINK, M .

HISTOPATHOLOGY, 1993, 23 (06) :557-561

← 1 2 →