Cellular Classification
Cytogenetic Changes in the Ewing Family of Tumors
Ewing family of tumors (EFT) belong to the group of neoplasms
commonly referred to as small, round, blue-cell tumors of childhood. The MIC2
gene product, CD99, is a surface membrane protein that is expressed in most
cases of EFT and is useful in suggesting diagnosis
of these tumors when the results are interpreted in the context of clinical and
pathologic parameters.[1] MIC2 positivity is not unique to EFT, and
positivity by immunochemistry is found in several other tumors including
synovial sarcoma, non-Hodgkin lymphoma, and gastrointestinal stromal tumors. Concurrent positivity for membrane CD99 and FL-1 strongly suggest the diagnosis of EFT.[1] The detection of a translocation involving the EWS gene on chromosomes 22 band q12 and any one of a number of partner chromosomes is the key feature in the diagnosis of EFT.[2]
The individual cells of EFT contain round-to-oval nuclei with fine dispersed chromatin without nucleoli. Occasionally, cells with smaller, more hyperchromatic, and probably degenerative nuclei are present giving a light cell/dark cell pattern. The cytoplasm varies in amount, but in the classic case it is clear and contains glycogen, which can be highlighted with a periodic acid-Schiff (PAS) stain. The tumor cells are tightly packed and grow in a diffuse pattern without evidence of structural organization. Tumors with the requisite translocation that show neuronal differentiation are not considered a separate entity, but rather, part of a continuum of differentiation.
Cytogenetic Changes in the Ewing Family of Tumors
Cytogenetic studies of the EFT have identified a consistent alteration of the
EWS locus on chromosome 22 band q12 that may involve other chromosomes,
including 11 or 21.[3] Characteristically, the amino terminus of the EWS
gene is juxtaposed with the carboxy terminus of another gene. In most cases (90%), the carboxy terminus is provided by FLI1, a member of
the Ets family of transcription factors gene located on chromosome 11 band q24.
Other Ets family members that may combine with the EWS gene in order of
frequency are ERG, located on chromosome 21; ETV 1, located on chromosome 7;
and E1AF, located on chromosome 17; these result in the following
translocations: t(21:22),[4] t(7;22), and t(17;22), respectively. Besides these
consistent aberrations involving the EWS gene at 22q12, additional numerical
and structural aberrations have been observed in EFTs, including gains of
chromosomes 2, 5, 8, 9, 12, and 15; the nonreciprocal translocation
t(1;16)(q12;q11.2); and deletions on the short arm of chromosome 6. A
molecular test (i.e., reverse transcription polymerase chain reaction [RT-PCR] and restriction analysis of PCR products), currently
available on a research basis only, now offers the opportunity of markedly
simplifying the definition of the EFT.[5,6] The molecular assay can be
performed on relatively small amounts of tissue obtained by minimally invasive
biopsies and is capable of providing results faster than cytogenetic analysis.
References
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Parham DM, Hijazi Y, Steinberg SM, et al.: Neuroectodermal differentiation in Ewing's sarcoma family of tumors does not predict tumor behavior. Hum Pathol 30 (8): 911-8, 1999.
[PUBMED Abstract]
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Delattre O, Zucman J, Melot T, et al.: The Ewing family of tumors--a subgroup of small-round-cell tumors defined by specific chimeric transcripts. N Engl J Med 331 (5): 294-9, 1994.
[PUBMED Abstract]
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Urano F, Umezawa A, Yabe H, et al.: Molecular analysis of Ewing's sarcoma: another fusion gene, EWS-E1AF, available for diagnosis. Jpn J Cancer Res 89 (7): 703-11, 1998.
[PUBMED Abstract]
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Hattinger CM, Rumpler S, Strehl S, et al.: Prognostic impact of deletions at 1p36 and numerical aberrations in Ewing tumors. Genes Chromosomes Cancer 24 (3): 243-54, 1999.
[PUBMED Abstract]
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Meier VS, Kühne T, Jundt G, et al.: Molecular diagnosis of Ewing tumors: improved detection of EWS-FLI-1 and EWS-ERG chimeric transcripts and rapid determination of exon combinations. Diagn Mol Pathol 7 (1): 29-35, 1998.
[PUBMED Abstract]
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Dagher R, Pham TA, Sorbara L, et al.: Molecular confirmation of Ewing sarcoma. J Pediatr Hematol Oncol 23 (4): 221-4, 2001.
[PUBMED Abstract]
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