Lower- and higher-grade subtypes of diffuse gastric cancer

被引:18
作者
Chiaravalli, Anna Maria [1 ,2 ,3 ]
Klersy, Catherine [4 ]
Tava, Francesca [5 ]
Manca, Rachele [5 ]
Fiocca, Roberto [6 ]
Capella, Carlo [1 ,2 ,3 ]
Solcia, Enrico [5 ]
机构
[1] Univ Insubria, Dept Human Morphol, I-21100 Varese, Italy
[2] Univ Insubria, Ctr Insubre Biotecnol Salute Umana, I-21100 Varese, Italy
[3] Osped Circolo Varese, I-21100 Varese, Italy
[4] Fdn IRCCS Policlin San Matteo, Sci Direct, Unit Biometry & Clin Epidemiol, I-27100 Pavia, Italy
[5] Univ Pavia, Dept Human Pathol, I-27100 Pavia, Italy
[6] Univ Genoa, Dept Surg & Morphol Sci, I-16132 Genoa, Italy
关键词
Diffuse desmoplastic cancer; Tumor embedding desmoplasia; Diffuse anaplastic cancer; Histology; Prognosis; SOFT-TISSUE SARCOMAS; STEM-CELLS; UNDIFFERENTIATED SARCOMAS; MESENCHYMAL TUMOR; RHABDOMYOSARCOMA; EXPRESSION; EXPERIENCE; BEHAVIOR; INFANCY; FUSION;
D O I
10.1016/j.humpath.2009.04.004
中图分类号
R36 [病理学];
学科分类号
100103 [病原生物学];
摘要
Diffuse gastric cancer, characterized by poorly cohesive, diffusely infiltrating cells with no or little gland formation, is known to show several morphologic variants, but their prognostic value, if any, is poorly documented. In this article, 119 cases of invasive (T1 b to T4) diffuse gastric cancer, which had undergone potentially curative surgery and were followed postoperatively for a median time of more than 10 years, were investigated for histologic or histochemical patterns possibly predictive of survival. Among 5 histologic groups identified, a low-grade subtype (17 cases) with prominent desmoplasia closely surrounding individual tumor cells (tumor embedding desmoplasia) and no or scarce angio-lympho-neuroinvasion showed stage-independent improved survival compared with 36 non-low-grade desmoplastic, 24 signet ring, and 28 diffuse cancers not otherwise specified. Fourteen cases with anaplastic cells showed clinicopathologic patterns and outcome of highly malignant neoplasms. None of the tumor cell differentiation markers (including 6 mucins and 3 proteases) nor proliferative index or p53 protein expression had independent predictive power, although MUC1 was significantly less expressed in low-grade desmoplastic cases. Cox survival analysis showed the significantly better prognosis of 17 low-grade desmoplastic and worse prognosis of 14 anaplastic cancers compared with the remaining 88 cases. In conclusion, a low-grade desmoplastic and a high-grade anaplastic subtype should be separated histologically from the bulk of diffuse gastric cancers owing to their distinctive histologic, clinicopathologic, and prognostic aspects. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:1591 / +
页数:18
相关论文
共 38 条
[1]
Alaggio R, 2006, AM J SURG PATHOL, V30, P388
[2]
Allaggio R, 2008, MODERN PATHOL, V21, p332A
[3]
Superficial low-grade fibromyxoid sarcoma (Evans tumor) - A clinicopathologic analysis of 19 cases with a unique observation in the pediatric population [J].
Billings, SD ;
Giblen, G ;
Fanburg-Smith, JC .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2005, 29 (02) :204-210
[4]
Angiogenesis in cancer and other diseases [J].
Carmeliet, P ;
Jain, RK .
NATURE, 2000, 407 (6801) :249-257
[5]
SO-CALLED CONGENITAL-INFANTILE FIBROSARCOMA - DOES IT EXIST AND WHAT IS IT [J].
COFFIN, CM ;
JASZCZ, W ;
OSHEA, PA ;
DEHNER, LP .
PEDIATRIC PATHOLOGY, 1994, 14 (01) :133-150
[6]
Fletcher ChristopherDM., 2002, PATHOLOGY GENETICS T, V4
[7]
GONZALEZ-CRUSSI F, 1979, American Journal of Surgical Pathology, V3, P157, DOI 10.1097/00000478-197904000-00008
[8]
Practical application of molecular genetic testing as an aid to the surgical pathologic diagnosis of sarcomas - A prospective study [J].
Hill, DA ;
O'Sullivan, MJ ;
Zhu, XP ;
Vollmer, RT ;
Humphrey, PA ;
Dehner, LP ;
Pfeifer, JD .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2002, 26 (08) :965-977
[9]
Immunohistochemical analysis of hSNF5/INI1 distinguishes renal and extra-renal malignant rhabdoid tumors from other pediatric soft tissue tumors [J].
Hoot, AC ;
Russo, P ;
Judkins, AR ;
Perlman, EJ ;
Biegel, JA .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2004, 28 (11) :1485-1491
[10]
A novel ETV6-NTRK3 gene fusion in congenital fibrosarcoma [J].
Knezevich, SR ;
McFadden, DE ;
Tao, W ;
Lim, JF ;
Sorensen, PHB .
NATURE GENETICS, 1998, 18 (02) :184-187