E. Hauben et al., Adamantinoma-like Ewing's sarcoma and Ewing's-like adamantinoma. The t(11;22), t(21;22) status, J PATHOLOGY, 195(2), 2001, pp. 218-221
Citations number
39
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Medical Research Diagnosis & Treatment
Adamantinoma of the long bones and Ewing's sarcoma are two malignant tumour
s between which, at first sight, there seems to be no morphological and cli
nical relationship. Both tumours, however. are known to express cytokeratin
s. Adamantinoma is a tumour of true epithelial nature, predominantly expres
sing cytokeratins 14 and 19. Ewing's sarcoma, believed to be from neuroecto
dermal origin, like other mesenchymal tumours, can aberrantly express cytok
eratin 8 and 18. In the literature there are some reports of tumours showin
g clinical and/or morphological overlap between adamantinoma and Ewing's sa
rcoma, suggesting a possible relationship. These studies are mostly based o
n the epithelioid configuration of these lesions and their cytokeratin expr
ession on immunohistochemistry. This raises the question of whether there i
s occasionally a morphological similarity between adamantinoma and Ewing's
sarcoma, or whether there is a common genetic background. The Ewing's sarco
ma/primitive peripheral neuroectodermal tumour (PN ET) family is characteri
zed in 90-95% of cases by a t(11; 22) and in 5-10% of cases by t(21; 22). I
n the few reports in the literature on cytogenetic investigations on adaman
tinoma, these translocations were never found using classical karyotyping.
This study investigated the putative presence of t(11; 22) and t(21; 22) in
14 cases of adamantinoma by RT-PCR. These translocations ere not found in
any of these cases. The results support the view that these tumours are gen
etically and clinically distinct, but may eventually show overlapping morph
ological and immunohistochemical features. Copyright (C) 2001 John Wiley &
Sons, Ltd.