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
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.