Shanks J H, Banerjee S S
Department of Histopathology, Christie Hospital NHS Trust, Withington, Manchester.
J Clin Pathol. 1996 Mar;49(3):205-7. doi: 10.1136/jcp.49.3.205.
To investigate the immunoreactivity of a range of melanocytic lesions, both benign and malignant, with the monoclonal antibody VS38. This was recently described as a marker of reactive/neoplastic plasma cells and, therefore, is useful in the diagnosis of plasmacytoma/myeloma and lymphomas with plasmacytic differentiation. This study was prompted by the recent observation that a plasmacytoid melanoma arising in the nasal cavity was strongly immunoreactive with VS38, which was therefore a potential source of major diagnostic error.
The Streptavidin-peroxidase complex technique was used on paraffin wax embedded sections of 167 melanocytic lesions. Diaminobenzidine (DAB) was used as chromogen for non-pigmented or lightly pigmented lesions and nickel/DAB for more heavily pigmented lesions.
Positive immunostaining for VS38 was seen in 14.5% (10/69) of benign naevi (including 40% (four of 10) of Spitz naevi), 10.5% (two of 19) of dysplastic naevi/in situ melanomas, 92% (35/38) of primary cutaneous melanomas, 100% (four of four) of primary mucosal melanomas, 91.7% (33/36) of recurrent/metastatic melanomas, and 100% (one of one) of clear cell sarcomas of soft tissues.
VS38 immunostaining is frequently positive in primary 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 at unusual sites, such as in the nasal cavity. The possibility of malignant melanoma should be actively considered and excluded in any undifferentiated tumour which shows VS38 immunoreactivity.
研究一系列良性和恶性黑素细胞性病变与单克隆抗体VS38的免疫反应性。VS38最近被描述为反应性/肿瘤性浆细胞的标志物,因此在浆细胞瘤/骨髓瘤以及具有浆细胞分化的淋巴瘤的诊断中很有用。本研究是受最近一项观察结果的启发,即鼻腔中发生的浆细胞样黑色素瘤与VS38呈强免疫反应性,因此这可能是主要诊断错误的一个潜在来源。
对167例黑素细胞性病变的石蜡包埋切片采用链霉亲和素-过氧化物酶复合物技术。对于无色素或色素较轻的病变,使用二氨基联苯胺(DAB)作为显色剂;对于色素较重的病变,使用镍/DAB。
在14.5%(10/69)的良性痣(包括40%(10例中的4例)的Spitz痣)、10.5%(2/19)的发育异常痣/原位黑色素瘤、92%(35/38)的原发性皮肤黑色素瘤、100%(4/4)的原发性黏膜黑色素瘤、91.7%(33/36)的复发性/转移性黑色素瘤以及100%(1/1)的软组织透明细胞肉瘤中观察到VS38免疫染色阳性。
VS38免疫染色在原发性和复发性/转移性恶性黑色素瘤中常呈阳性,在良性痣中也较少出现反应性。当使用这种最近描述的正常/肿瘤性浆细胞标志物来识别肿瘤谱系时,应牢记这些结果,尤其是在不寻常部位发生的肿瘤,如鼻腔。在任何显示VS38免疫反应性的未分化肿瘤中,都应积极考虑并排除恶性黑色素瘤的可能性。