BACKGROUND. The authors became interested in an association between cu
taneous melanoma and sarcoma when they reviewed their experience with
other malignancies occurring in patients with a diagnosis of sarcoma.
METHODS. The authors identified 48 patients with both melanoma and bon
e or soft tissue sarcoma (STS) by a computer search of all sarcoma pat
ients entered into their institution's cancer registry between 1943 an
d 1996 who had an additional diagnosis of melanoma. The medical record
s were reviewed and clinical and pathologic data collected. RESULTS. T
he median age at diagnosis was 46 years for patients with melanoma and
50 years for patients with sarcoma, which was consistent with populat
ion-based data. Among patients with STS (n = 41), malignant peripheral
nerve sheath tumors (MPNT) were more common in patients with both dia
gnoses (5 of 41; 13%) when compared with all adults with STS admitted
to the study center between 1982 to date (125 of 2901; 4%; P < 0.05).
Liposarcoma occurred in only 1 patient with both melanoma and STS (1 o
f 41; 2%), despite the fact that it was the most common histologic dia
gnosis in all adults with STS (625 of 2901; 22%; P < 0.001). The anato
mic site of STS was more commonly visceral (11 of 41; 27%) when compar
ed with all adults with STS (424 of 2901; 15%; P < 0.05). A positive f
amily history of cancer was noted in 50% of the patients, and 25% of p
atients had a third primary tumor. CONCLUSIONS. Although a distinct ''
melanoma/sarcoma'' syndrome was not identified, MPNT as well as viscer
al sarcomas were more common than expected in this study. The authors
also noted strong family histories of cancer as well as additional pri
mary malignancies in patients with melanoma and sarcoma, suggesting a
predisposition toward cancer. (C) 1997 American Cancer Society.