O. Benizhak et al., ANORECTAL MALIGNANT-MELANOMA - A CLINICOPATHOLOGICAL STUDY, INCLUDINGIMMUNOHISTOCHEMISTRY AND DNA FLOW-CYTOMETRY, Cancer, 79(1), 1997, pp. 18-25
BACKGROUND, Anorectal malignant melanoma is a rare tumor with an extre
mely poor prognosis. DNA flow cytometric study as well as detailed imm
unohistochemical study have not been reported previously. METHODS, Eig
hteen cases of anorectal melanoma were studied, including immunohistol
ogy for melanoma markers and epithelial markers and DNA flow cytometri
c study of paraffin blocks. RESULTS. Most patients were Ashkenazi Jews
, compared with Sephardi Jews and Arabs. Of the 17 patients followed,
14 died of disease at 4-39 months from presentation. Three patients we
re alive with disease at 12, 53, and 72 months of follow-up. Tumor thi
ckness ranged from 3-35 mm (mean, 12.8 mm). The 2 long term survivors
had tumor thickness less than or equal to 7 mm. No correlation was fou
nd between the mode of primary surgical treatment (8 patients: abdomin
operineal resection; 10 patients: local excision) and outcome. Vimenti
n, HMB-45, and S-100 protein stainings were positive in 18, 17, and 15
tumors, respectively. Polyclonal carcinoembryonic antigen (CEA), broa
d-spectrum cytokeratin, epithelial membrane antigen, monoclonal CEA, a
nd TAG-72 (B72.3) stainings were positive in 13, 3 (only focal and rar
e staining), 2, 0, and 0 tumors, respectively. Thirteen tumors had ade
quate material for DNA analysis, and all were DNA aneuploid. S-phase f
raction could be assessed in 11 tumors and ranged from 7.7-24% (mean,
14%). An S-phase fraction of < 10% was observed in the 2 long term sur
vivors. CONCLUSIONS. Anorectal melanoma in this study carried a grave
prognosis. The frequent staining for polyclonal CEA (with negative mon
oclonal CEA staining) was probably due to nonspecific cross-reacting a
ntigens. The occasional staining for epithelial markers warrants a com
prehensive immunohistochemical study to ensure a correct diagnosis, es
pecially in small biopsies of amelanotic undifferentiated tumors that
lack junctional changes. The aneuploidy of all tested tumors reflected
their highly malignant behavior. A trend toward longer survival was o
bserved in patients with thin tumors and an S-phase fraction of < 10%.
However, due to the small number of survivors, the latter observation
should be further tested in a larger scale series. (C) 1997 American
Cancer Society.