Abstract:Acral lentiginous melanoma (ALM) is the fourth clinicopathologic variant of malignant melanoma. It occurs on volar surfaces of hands and feet, subungual sites, and fingers or toes. It is characterized by slow lentiginous radial growth and central plaque-like thickening, heavily pigmented tumor cells, markedly thickened papillary dermis, and diffuse reticular infiltration. Lesions are unusually large and, in most cases, thick and ulcerated. There were 180 patients with acral melanoma (AM), which includes 67 in … Show more
“…The classification of MM into types has been the topic of much debate in the recent literature (Lieblich, 1982, Rampen, 1983). Proponents of the concept claim that certain subsets of MM have distinct clinical, cellular and behavioral characteristics as well as different cumulative survival rates (Bigotti et al, 1981; Clark et al, 1986; Holman and Armstrong, 1984a; Jimbow et al, 1984; Krementz et al, 1982; Larsen and Grude, 1978a‐c; McGovern and Murad, 1985; Milton et al, 1985a; Roberts et al, 1981; Shiftman et al, 1980; Sondergaard, 1983).…”
Section: Discussionmentioning
confidence: 99%
“… Blois et al, 1983b; Clark 1967; Clark et al, 1975, 1986; Donnellan et al, 1972; Elder et al, 1982; Goldman, 1980; Harwood, 1983; Heenan and Holman, 1982; Jeffrey et al, 1983; Jimbow et al, 1984; Johnson et al, 1985; Koh et al, 1984b; Krementz et al, 1982; Paladugu et al, 1983; Papachristou and Fortner, 1982; Roberts et al, 1981; Seiji et al, 1979; Sober et al, 1980; Sondergaard, 1983; Takematsu et al, 1985; Vazquez et al, 1984; Wade and White, 1986. …”
“…The classification of MM into types has been the topic of much debate in the recent literature (Lieblich, 1982, Rampen, 1983). Proponents of the concept claim that certain subsets of MM have distinct clinical, cellular and behavioral characteristics as well as different cumulative survival rates (Bigotti et al, 1981; Clark et al, 1986; Holman and Armstrong, 1984a; Jimbow et al, 1984; Krementz et al, 1982; Larsen and Grude, 1978a‐c; McGovern and Murad, 1985; Milton et al, 1985a; Roberts et al, 1981; Shiftman et al, 1980; Sondergaard, 1983).…”
Section: Discussionmentioning
confidence: 99%
“… Blois et al, 1983b; Clark 1967; Clark et al, 1975, 1986; Donnellan et al, 1972; Elder et al, 1982; Goldman, 1980; Harwood, 1983; Heenan and Holman, 1982; Jeffrey et al, 1983; Jimbow et al, 1984; Johnson et al, 1985; Koh et al, 1984b; Krementz et al, 1982; Paladugu et al, 1983; Papachristou and Fortner, 1982; Roberts et al, 1981; Seiji et al, 1979; Sober et al, 1980; Sondergaard, 1983; Takematsu et al, 1985; Vazquez et al, 1984; Wade and White, 1986. …”
“…Another more interesting possibility is that the dierent type of melanoma examined in both studies might be responsible for the dierent frequency of LOH of 9p21-22. More than half of our samples were acral melanomas which are the main type of melanoma in Japanese and dier from other types of melanomas in clinical characteristics (Krementz et al, 1982;Seiji et al, 1979) and in antigenic pro®le (Kageshita et al, 1991). Although we did not ®nd signi®cant dierence in frequency of LOH between acral and non-acral melanomas in our limited number of cases, the unexpectedly low frequency of allelic loss on chromosome arm 9p in acral melanomas (5/28; 18%) raises the possibility that the genetic pathways to this particular type of melanoma might be dierent from those to non-acral melanomas commonly seen in Caucasians.…”
In an attempt to examine whether the inactivation of p16INK4a is an important early event in the development of sporadic melanoma in vivo, we have systematically analysed 46 uncultured primary cutaneous melanomas. Loss of heterozygosity (LOH) of chromosome region 9p21-22 (where the p16INK4a resides) was detected in 11 tumours (24%) by PCR-based LOH analyses. Direct sequencing of all three exons of the p16INK4a gene in these 11 tumours revealed no somatic mutation although germline mutations which have not been reported previously as common polymorphisms were detected in two patients. Further sequencing analyses of the p16 INK4a protein, most likely due to homozygous deletion of the p16INK4a gene, was observed in 6 (15%) out of 39 evaluable cases by immunohistochemical analyses on frozen sections using two dierent anti-p16INK4a antibodies. The results show that inactivation of p16INK4a is not as frequent in primary melanoma as has been reported in cell lines, and warrant further search for another tumour suppressor on 9p21-22. This study also emphasizes the importance of examining uncultured primary tumours rather than cell lines to de®ne early events in tumorigenesis.
“…The influence of lymph node involvement could not be Rushforth reported an incidence of 2.55 per l~, m ascertained since regional node dissection was performed 2-3% of patients with malignant melanoma in several The purpose of this study was to evaluate subungual large series [4-71, B~~~~~~ of its rarity subungual mela-melanoma as a site-specific entity, to determine the influnoma has been commonly described in reports as ence of regional nodal involvement and to ascertain where part of larger series describing extremity melanomas or possible the role of histologic grading of the primary site. as clinicopathologic variants of malignant melanoma such as acral lentiginous melanoma [4][5][6][7][8]. Recent advances in the management of melanoma have been made through From l950 to lg759 33 patients with subungual melahowledge of determinants such as primary depth of noma underwent treatment at Memorial Sloan-Kettering invasion, thickness, presence of ulceration, stabs of re-Cancer Center.…”
The purpose of this study was to evaluate subungual melanoma as a site-specific entity, to determine the influence of regional nodal involvement, and to ascertain where possible the role of histologic grading of the primary site. Thirty-three patients with subungual melanoma whose median age was 56 yr underwent treatment between 1950 and 1975. There were 11 male and 22 female patients. Forty-eight per cent of lesions were 11 male and 22 female patients. Forty-eight per cent of lesions occurred on the hand. Of 23 clinical stage I patients, seven patients underwent amputation only, while 16 patients underwent amputation and regional nodal dissection. Histologic examination of the primary tumor suggested a trend towards thicker/ulcerated lesions to be associated with metastatic melanoma in regional lymph nodes and/or death due to disease. Early survival patterns favored female patients but there was no significant difference in 10-year survival when analysed by patient sex. Clinical/pathologic stages were the most significant factors affecting long-term survival with 5- and 10-year survivals of 66% and 55% in stage I patients and 22% and 0% in stage II patients.
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