Electrical impedance scanning: a new approach to skin cancer diagnosis

被引:52
作者
Glickman, YA
Filo, O
David, M
Yayon, A
Topaz, M
Zamir, B
Ginzburg, A
Rozenman, D
Kenan, G
机构
[1] TransScan Med Ltd, IL-10550 Migdal Haemeq, Israel
[2] Weizmann Inst Sci, Dept Mol Cell Biol, IL-76100 Rehovot, Israel
[3] Hillel Yaffe Med Ctr, Plast Surg Unit, Hadera, Israel
[4] Ibn Sina Clin, Dept Dermatol, Haifa, Israel
[5] Dermatol Clin, Raanana, Israel
[6] Haemek Med Ctr, Dept Dermatol, Afula, Israel
关键词
electrical impedance scanning; conductivity melanoma; skin cancer; pigmented lesion;
D O I
10.1034/j.1600-0846.2003.00022.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background/aims: Skin cancer diagnosis depends, to a great extent, on visual inspection and histopathological examination of excised tissues. The aim of this study is to evaluate the ability of electrical impedance scanning to differentiate between benign and malignant skin lesions. Methods: A preclinical study was conducted on 40 nude mice injected subcutaneously with a human melanoma strain. Impedance measurements were recorded every week to correlate electrical changes with tumor growth and histological findings. A clinical study was also performed on 178 human suspicious skin lesions before excision. The impedance measurements were correlated to the histopathological results. Results: Normalized conductivity and capacitance, recorded on growing skin tumors in nude mice, were shown to change relative to lesion size. Necrosis, present in most of the larger lesions, was associated with a decrease in the electrical conductivity. Similar electrical parameters were used to classify human melanoma lesions with 92% sensitivity and 67% specificity. In addition, four out of five BCC lesions were correctly diagnosed. Moreover, dysplastic lesions were diagnosed with 91% sensitivity and 59% specificity. For comparison, physicians diagnosed melanoma lesions with 75% sensitivity and 87% specificity and dysplastic lesions with 46% sensitivity and 80% specificity. Conclusions: The animal study showed that electrical impedance measurements reflect morphological changes related to the growth of a cancerous skin lesion. These findings are in agreement with a preliminary clinical study. Electrical Impedance Scanning can therefore be considered as an objective and non-invasive tool for differentiation between benign and malignant skin lesions.
引用
收藏
页码:262 / 268
页数:7
相关论文
共 37 条
[1]  
ACKERMAN AB, 1985, HUM PATHOL, V16, P87
[2]   Digital dermoscopy analysis for the differentiation of atypical nevi and early melanoma - A new quantitative semiology [J].
Andreassi, L ;
Perotti, R ;
Rubegni, P ;
Burroni, M ;
Cevenini, G ;
Biagioli, M ;
Taddeucci, P ;
Dell'Eva, G ;
Barbini, P .
ARCHIVES OF DERMATOLOGY, 1999, 135 (12) :1459-1465
[3]  
[Anonymous], HDB MED IMAGING
[4]   Dermoscopy of pigmented skin lesions - a valuable tool for early diagnosis of melanoma [J].
Argenziano, Giuseppe ;
Soyer, H. Peter .
LANCET ONCOLOGY, 2001, 2 (07) :443-449
[5]   The T-SCAN™ technology:: electrical impedance as a diagnostic tool for breast cancer detection [J].
Assenheimer, M ;
Laver-Moskovitz, O ;
Malonek, D ;
Manor, D ;
Nahaliel, U ;
Nitzan, R ;
Saad, A .
PHYSIOLOGICAL MEASUREMENT, 2001, 22 (01) :1-8
[6]  
BALCH CM, 1998, CUTANEOUS MELANOMA, P12
[7]   Diagnostic ability of general practitioners and dermatologists in discriminating pigmented skin lesions [J].
Brochez, L ;
Verhaeghe, E ;
Bleyen, L ;
Naeyaert, JM .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2001, 44 (06) :979-986
[8]  
Brown N, 2000, Clin Excell Nurse Pract, V4, P263
[9]   Automatic differentiation of melanoma from melanocytic nevi with multispectral digital dermoscopy: A feasibility study [J].
Elbaum, M ;
Kopf, AW ;
Rabinovitz, HS ;
Langley, RGB ;
Kamino, H ;
Mihm, MC ;
Sober, AJ ;
Peck, GL ;
Bogdan, A ;
Gutkowitcz-Krusin, D ;
Greenebaum, M ;
Keem, S ;
Oliviero, M ;
Wang, S .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2001, 44 (02) :207-218
[10]   Electrical impedance of nodular basal cell carcinoma:: A pilot study [J].
Emtestam, L ;
Nicander, I ;
Stenström, M ;
Ollmar, S .
DERMATOLOGY, 1998, 197 (04) :313-316