Staining of melanocytic neoplasms by melanoma antigen recognized by T cells

被引:8
作者
Mehregan, DR
Hamzavi, I
机构
[1] Pinkus Dermatopathol Lab, Monroe, MI USA
[2] Wayne State Univ, Detroit, MI USA
关键词
immunohistochemistry; Mart-1; melanoma; melanoma antigen related to T cells; nevus; pathology; spitz nevus;
D O I
10.1097/00000372-200006000-00007
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
We stained benign melanocytic nevi and malignant melanoma with antibodies to melanoma antigen recognized by T cells (Mart-1) to determine if this was useful in differentiating benign from malignant melanocytic neoplasms. Forty-five primary malignant melanomas and 71 benign melanocytic nevi were stained with antibodies to Mart-1. Two cases of malignant melanoma metastatic to lymph node and three cutaneous metastases of malignant melanoma were also stained. The degree of staining was graded into diffuse positive staining, focal positive staining, and negative staining, Thirty-six of 45 primary malignant melanomas stained diffusely positive with antibodies to Mart-1. This included three of five desmoplastic malignant melanomas that showed positive staining. Four melanomas showed faint or focal positive staining. One of two metastases to lymph node showed strong positive staining and one showed no staining. All three cutaneous metastases showed diffuse positive staining. Sixty-one of 71 melanocytic nevi showed no staining or faint staining with antibodies to Mart-1. Ten of 71 melanocytic nevi showed strong positive staining. The majority of these were congenital nevi. Staining with antibodies to Mart-1 antigen was a useful marker of malignant melanoma. However, staining may also be seen in benign melanocytic neoplasms. The presence or absence of staining for Mart-1 antigen cannot be used to differentiate benign melanocytic nevi from malignant melanocytic tumors.
引用
收藏
页码:247 / 250
页数:4
相关论文
共 18 条
[1]   Silver-stained nucleolar organizer regions (AgNORs) as a prognostic value in malignant melanoma [J].
Barzilai, A ;
Goldberg, I ;
Yulash, M ;
Pavlotsky, F ;
Zuckerman, A ;
Trau, H ;
Azizi, E ;
Kopolovic, J .
AMERICAN JOURNAL OF DERMATOPATHOLOGY, 1998, 20 (05) :473-477
[2]  
Beaty MW, 1997, CANCER CYTOPATHOL, V81, P57, DOI 10.1002/(SICI)1097-0142(19970225)81:1<57::AID-CNCR12>3.0.CO
[3]  
2-B
[4]  
BJORNHAGEN V, 1994, AM J DERMATOPATH, V16, P615
[5]   Comparative analysis of the in vivo expression of tyrosinase, MART-1/Melan-A, and gp100 in metastatic melanoma lesions: Implications for immunotherapy [J].
Cormier, JN ;
Abati, A ;
Fetsch, P ;
Hijazi, YM ;
Rosenberg, SA ;
Marincola, FM ;
Topalian, SL .
JOURNAL OF IMMUNOTHERAPY, 1998, 21 (01) :27-31
[6]  
deVries TJ, 1997, CANCER RES, V57, P3223
[7]   Immunocytochemical detection of MART-1 in fresh and paraffin-embedded malignant melanomas [J].
Fetsch, PA ;
Cormier, J ;
Hijazi, YM .
JOURNAL OF IMMUNOTHERAPY, 1997, 20 (01) :60-64
[8]   Minimally invasive staging of patients with melanoma: Sentinel lymphadenectomy and detection of the melanoma-specific proteins MART-1 and tyrosinase by reverse transcriptase polymerase chain reaction [J].
Goydos, JS ;
Ravikumar, TS ;
Germino, FJ ;
Yudd, A ;
Bancila, E .
JOURNAL OF THE AMERICAN COLLEGE OF SURGEONS, 1998, 187 (02) :182-188
[9]   Differential expression of MART-1 in primary and metastatic melanoma lesions [J].
Kageshita, T ;
Kawakami, Y ;
Hirai, S ;
Ono, T .
JOURNAL OF IMMUNOTHERAPY, 1997, 20 (06) :460-465
[10]   Production of recombinant MART-1 proteins and specific antiMART-1 polyclonal and monoclonal antibodies: Use in the characterization of the human melanoma antigen MART-1 [J].
Kawakami, Y ;
Battles, JK ;
Kobayashi, T ;
Ennis, W ;
Wang, X ;
Tupesis, JP ;
Marincola, FM ;
Robbins, PF ;
Hearing, VJ ;
Gonda, MA ;
Rosenberg, SA .
JOURNAL OF IMMUNOLOGICAL METHODS, 1997, 202 (01) :13-25