Epithelioid sarcoma a clinicopathologic and immunohistochemical analysis of 106 cases from the french sarcoma group

American Journal of Clinical Pathology

Volumn 131, Issue 2, 2009, Pages 222-227

  Chbani, Laila ^a   Guillou, Louis ^b   Terrier, Philippe ^c   Decouvelaere, Anne Valérie ^d   Grégoire, Fleur ^e   Terrier Lacombe, Marie José ^c   Ranchère, Dominique ^d   Robin, Yves Marie ^f   Collin, Françoise ^g   Fréneaux, Paul ^a   Coindre, Jean Michel ^a,h  

^a INSTITUT BERGONIÉ   (France)

^b INSTITUT GUSTAVE ROUSSY   (France)

^c CENTRE LÉON BÉRARD   (France)

^d CENTRE OSCAR LAMBRET   (France)

^e CENTRE GEORGES FRANÇOIS LECLERC   (France)

^f INSTITUT CURIE   (France)

^g UNIVERSITY INSTITUTE OF PATHOLOGY   (Switzerland)

^h UNIVERSITÉ DE BORDEAUX   (France)

Author keywords

Epithelioid sarcoma; INI1; Prognosis

Indexed keywords

ARTICLE; CANCER CLASSIFICATION; CONTINUING EDUCATION; EPITHELIOID SARCOMA; FRANCE; HUMAN; IMMUNOHISTOCHEMISTRY; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; PROGNOSIS; SOFT TISSUE SARCOMA; TUMOR SUPPRESSOR GENE; ADOLESCENT; ADULT; AGED; CHEMISTRY; CHILD; FEMALE; MALE; MIDDLE AGED; MITOSIS INDEX; MORTALITY; MULTIMODALITY CANCER THERAPY; PATHOLOGY; SARCOMA; SOFT TISSUE TUMOR; SURVIVAL RATE;

DNA BINDING PROTEIN; NONHISTONE PROTEIN; SMARCB1 PROTEIN, HUMAN; TRANSCRIPTION FACTOR; TUMOR MARKER;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; CHILD; CHROMOSOMAL PROTEINS, NON-HISTONE; COMBINED MODALITY THERAPY; DNA-BINDING PROTEINS; FEMALE; HUMANS; MALE; MIDDLE AGED; MITOTIC INDEX; SARCOMA; SOFT TISSUE NEOPLASMS; SURVIVAL RATE; TRANSCRIPTION FACTORS; TUMOR MARKERS, BIOLOGICAL; YOUNG ADULT;

EID: 58849101838     PISSN: 00029173     EISSN: None     Source Type: Journal    
DOI: 10.1309/AJCPU98ABIPVJAIV     Document Type: Article

References (17)

1. Enzinger FM. Epithelioid sarcoma: a sarcoma simulating a granuloma or a carcinoma. Cancer. 1970;26:1029-1041.
2. Chase DR, Enzinger FM. Epithelioid sarcoma: diagnosis, prognostic indicators, and treatment. Am J Surg Pathol. 1985;9:241-263.
3. Guillou L, Wadden C, Coindre JM, et al. "Proximal-type" epithelioid sarcoma, a distinctive aggressive neoplasm showing rhabdoid features: clinicopathologic, immunohistochemical, and ultrastructural study of a series. Am J Surg Pathol. 1997;21:130-146.
4. Versteege I, Sevenet N, Lange J, et al. Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer. Nature. 1998;394:203-206.
5. Biegel JA, Zhou JY, Rorke LB, et al. Germ-line and acquired mutations of INI1 in atypical teratoid and rhabdoid tumours. Cancer Res. 1999;59:74-79.
6. Modena P, Lualdi E, Facchinetti F, et al. SMARCB1/INI1 tumor suppressor gene is frequently inactivated in epithelioid sarcomas. Cancer Res. 2005;65:4012-4019.
7. Hornick JL, Dal Cin P, Fletcher CDM. Loss of INI1 expression is characteristic of both conventional and proximal type epithelioid sarcoma [abstract]. Mod Pathol. 2007;20:16A. Abstract 52.
8. Guillou L, Kaneko Y. Epithelioid sarcoma. In: Fletcher CDM, Unni KK, Mertens F, eds. Pathology and Genetics of Tumours of Soft Tissue and Bone. Lyon, France: IARC Press; 2002:205-207. World Health Organization Classification of Tumours.
9. Miettinen M, Fanburg-Smith JC, Virolainen M, et al. Epithelioid sarcoma: an immunohistochemical analysis of 112 classical and variant cases and a discussion of the differential diagnosis. Hum Pathol. 1999;30:934-942.
10. Bourdeaut F, Fréneaux P, Thuille B, et al. hSNF5/INI1- deficient tumours and rhabdoid tumours are convergent but not fully overlapping entities. J Pathol. 2007;211:323-330.
11. Hoot AC, Russo P, Judkins AR, et al. Immunohistochemical analysis of hSNF5/INI1 distinguishes renal and extra-renal malignant rhabdoid tumors from other pediatric soft tissue tumors. Am J Surg Pathol. 2004;28:1485-1491.
12. Sigauke E, Rakheja D, Maddox DL, et al. Absence of expression of SMARCB1/INI1 in malignant rhabdoid tumors of the central nervous system, kidneys and soft tissue: an immunohistochemical study with implications for diagnosis. Mod Pathol. 2006;19:717-725.
13. Halling AC, Wollan PC, Pritchard DJ, et al. Epithelioid sarcoma: a clinicopathologic review of 55 cases. Mayo Clin Proc. 1996;71:636-642.
14. Spillane AJ, Thomas JM, Fisher C. Epithelioid sarcoma: the clinicopathological complexities of this rare soft tissue sarcoma. Ann Surg Oncol. 2000;3:218-225.
15. Hasegawa T, Matsuno Y, Shimoda T, et al. Proximal-type epithelioid sarcoma: a clinicopathologic study of 20 cases. Mod Pathol. 2001;14:655-663.
16. Callister MD, Ballo MT, Pisters PW, et al. Epithelioid sarcoma: results of conservative surgery and radiotherapy. lnt J Radiat Oncol Biol Phys. 2001;51:384-391.
17. Baratti D, Pennacchioli E, Casali PG, et al. Epithelioid sarcoma: prognostic factors and survival in a series of patients treated at a single institution. Ann Surg Oncol. 2007;14:3542-3551.