Aims-To investigate the immunoreactivity of a range of melanocytic les
ions, both benign and malignant, with the monoclonal antibody VS38. Th
is was recently described as a marker of reactive/neoplastic plasma ce
lls and, therefore, is useful in the diagnosis of plasmacytoma/myeloma
and lymphomas with plasmacytic differentiation. This study was prompt
ed by the recent observation that a plasmacytoid melanoma arising in t
he nasal cavity was strongly immunoreactive with VS38, which was there
fore a potential source of major diagnostic error. Methods-The Strepta
vidin-peroxidase complex technique was used on paraffin wax embedded s
ections of 167 melanocytic lesions. Diaminobenzidine (DAB) was used as
chromogen for non-pigmented or lightly pigmented lesions and nickel/D
AB for more heavily pigmented lesions. Results-Positive immunostaining
for VS38 was seen in 14.5% (10/69) of benign naevi (including 40% (fo
ur of 10) of Spitz naevi), 10.5% (two of 19) of dysplastic naevi/in si
tu melanomas, 92% (35/38) of primary cutaneous melanomas, 100% (four o
f four) of primary mucosal melanomas, 91.7% (33/36) of recurrent/metas
tatic melanomas, and 100% (one of one) of clear cell sarcomas of soft
tissues. Conclusions-VS38 immunostaining is frequently positive in pri
mary and recurrent/metastatic malignant melanoma and is also reactive
less commonly with benign naevi. These results should be borne in mind
when this recently described marker of normal/neoplastic plasma cells
is used to identify tumour lineage, particularly in tumours arising a
t unusual sites, such as in the nasal cavity. The possibility of malig
nant melanoma should be actively considered and excluded in any undiff
erentiated tumour which shows VS38 immunoreactivity.