Undifferentiated Carcinoma With Osteoclastic Giant Cells (UCOCGC) of the Pancreas Associated With the Familial Atypical Multiple Mole Melanoma Syndrome (FAMMM)

被引:17
作者
Koorstra, Jan-Bart M. [1 ]
Maitra, Anirban [3 ]
Morsink, Folkert H. M. [1 ]
Drillenburg, Paul [2 ]
ten Kate, Fiebo J. W. [1 ]
Hruban, Ralph H.
Offerhaus, Johan A. [1 ]
机构
[1] Univ Med Ctr Utrecht, Dept Pathol, Utrecht, Netherlands
[2] Onze Lieve Vrouw Hosp, Amsterdam, Netherlands
[3] Johns Hopkins Univ, Sch Med, Johns Hopkins Med Inst, Sol Goldman Pancreat Canc Res Ctr, Baltimore, MD 21231 USA
关键词
undifferentiated carcinoma with osteoclastic giant cells; pancreas; familial atypical multiple mole melanoma syndrome; p16-Leiden deletion; KRAS2; codon; 12; mutation;
D O I
10.1097/PAS.0b013e31818371cd
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The familial atypical multiple mole melanoma (FAMMM) syndrome is caused by a germline mutation of p16. More than 90% of the sporadic pancreatic carcinomas contain genetic alterations that inactivate p16. Patients with the FAMMM syndrome have an increased risk of developing pancreatic cancer. Ductal adenocarcinoma is the most common cancer of the pancreas and the one encountered in patients with FAMMM syndrome. Undifferentiated carcinoma with osteoelastic giant cells, also referred to as UCOCGC of the pancreas, is a rare variant of pancreatic cancer. An UCOCGC of the pancreas associated with FAMMM syndrome is described in this report. Molecular analysis confirmed a germline p16-Leiden deletion in the UCOCGC, accompanied by somatic loss of heterozygosity of the second p16 allele, and absence of p16 protein expression in the neoplastic cells. It is the first case reported and it provides additional evidence that UCOCGC can be considered as a variant of conventional ductal adenocarcinoma of the pancreas.
引用
收藏
页码:1905 / 1909
页数:5
相关论文
共 14 条
[1]   Early undifferentiated pancreatic carcinoma with osteoclastlike giant cells: Direct evidence for ductal evolution [J].
Bergmann, Frank ;
Esposito, Irene ;
Michalski, Christoph W. ;
Herpel, Esther ;
Friess, Helmut ;
Schirmacher, Peter .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2007, 31 (12) :1919-1925
[2]  
Cappel WHDTN, 2003, CLIN CANCER RES, V9, P3598
[3]   INCREASED RISK OF PANCREATIC-CANCER IN MELANOMA-PRONE KINDREDS WITH P16(INK4) MUTATIONS [J].
GOLDSTEIN, AM ;
FRASER, MC ;
STRUEWING, JP ;
HUSSUSSIAN, CJ ;
RANADE, K ;
ZAMETKIN, DP ;
FONTAINE, LS ;
ORGANIC, SM ;
DRACOPOLI, NC ;
CLARK, WH ;
TUCKER, MA .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (15) :970-974
[4]   Excess cancer mortality in six Dutch pedigrees with the familial atypical multiple mole-melanoma syndrome from 1830 to 1994 [J].
Hille, ETM ;
van Duijn, E ;
Gruis, NA ;
Rosendaal, FR ;
Bergman, W ;
Vandenbroucke, JP .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1998, 110 (05) :788-792
[5]  
Hruban RH, 1997, AM J PATHOL, V151, P943
[6]  
KAMB A, 1994, SCIENCE, V264, P440
[7]   Pancreatic carcinogenesis [J].
Koorstra, Jan-Bart M. ;
Hustinx, Steven R. ;
Offerhaus, G. Johan A. ;
Maitra, Anirban .
PANCREATOLOGY, 2008, 8 (02) :110-125
[8]  
ROSAI J, 1968, CANCER, V22, P333, DOI 10.1002/1097-0142(196808)22:2<333::AID-CNCR2820220210>3.0.CO
[9]  
2-A
[10]  
Schutte M, 1997, CANCER RES, V57, P3126