MORPHOLOGIC DIVERSITY IN MALIGNANT-MELANOMA - THE POTENTIAL USE OF MICRODISSECTION AND THE POLYMERASE-CHAIN-REACTION FOR DIAGNOSIS

Citation
Mm. Quezado et al., MORPHOLOGIC DIVERSITY IN MALIGNANT-MELANOMA - THE POTENTIAL USE OF MICRODISSECTION AND THE POLYMERASE-CHAIN-REACTION FOR DIAGNOSIS, Modern pathology, 11(10), 1998, pp. 1010-1015
Citations number
41
Categorie Soggetti
Pathology
Journal title
ISSN journal
08933952
Volume
11
Issue
10
Year of publication
1998
Pages
1010 - 1015
Database
ISI
SICI code
0893-3952(1998)11:10<1010:MDIM-T>2.0.ZU;2-G
Abstract
Malignant melanoma (MM) can mimic soft tissue (ST) and epithelial neop lasms. An immunoperoxidase (IP) panel and a morphologic comparison of the primary are used in diagnosis, which can be difficult when the mor phologic and IP profiles of a metastatic lesion simulate those of an S T neoplasm. Through the comparison of known genetic abnormalities in p rimary and metastatic neoplasms, a definitive diagnosis can be suggest ed on the basis of the finding of identical allelic losses through the use of microdissection (MD) and the polymerase chain reaction (PCR). Genetic alterations involving the p16 gene on chromosome 9p21 have bee n observed in MM. We present the case of a 56-year-old man with known MM in whom multiple metastatic lesions to the skin and an adrenal glan d developed during a 5-year period. A fine-needle aspiration (FNA) of a new ST buttock lesion was performed; the specimen had cytologic feat ures different from those of the primary neoplasm and simulated a poss ible primary ST neoplasm, We attempted to make a definitive diagnosis of MM in the FNA of the ST buttock lesion through a genetic comparison with the primary neoplasm as well as with the other metastatic sites. Direct-visualization MD was performed on histologic glass slides of t he primary and adjacent tissue (normal control), and the metastatic le sions, along with malignant cell clusters from the buttock lesion FNA. DNA was extracted and PCR amplified with primers D9S171 and IFNA for the p16 locus at the 9p21-22 region. Loss of heterozygosity for the D9 S171 marker at the p16 gene locus was identified in all of the neoplas tic tissue tested. Normal skin elements did not show deletion. The com bination of MD and PCR are powerful tools that can be used for the com parison of genetic abnormalities in primary and metastatic neoplasms w ith unusual morphologic features to help support a diagnosis with a no ncontributory IF.