Possible histopathologic correlates of dermoscopic features in pigmented melanocytic lesions identified by means of optical coherence tomography

被引:39
作者
de Giorgi, V
Stante, M
Massi, D
Mavilia, L
Cappugi, P
Carli, P
机构
[1] Univ Florence, Dept Dermatol, I-50121 Florence, Italy
[2] Univ Florence, Dept Human Pathol & Oncol, I-50121 Florence, Italy
关键词
melanoma; OCT; dermoscopy; dermatoscopy; skin cancer;
D O I
10.1111/j.0906-6705.2005.00229.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Optical coherence tomography (OCT) is a novel non-invasive imaging technique for in vivo histologic characterization of tissues. Besides pure morphology, additional functional parameters of the tissue investigated can be evaluated at the same time, such as the refractive index and the scattering coefficient. The purpose of our study is to correlate in vivo the dermoscopic structures that first appear in the melanocytic pigmented lesion (pigment network and brown globules) using this new method, with the histopathologic correlates, in order to improve their characterization and achieve easier recognition and inter-observer reproducibility. We concentrated in particular on the pigment network and the brown globules, as these are dermoscopic parameters of great diagnostic importance in melanocytic lesions. Moreover, as these parameters are the histopathologic equivalents of structures located at the level of the dermo-epidermal junction, they enable a correct evaluation to be made using OCT, that at present has only a few millimetres penetration power. The results of our trial, performed using the histopathological preparation as an evaluation gold standard, show that in selected cases OCT allows an in vivo correlation to be made between surface dermoscopic parameters and histopathologic correlates, in particular the pigment network and brown globules. The resolution is not high enough to reveal the morphology of the single cells, but it is possible to evaluate the architecture of a lesion.
引用
收藏
页码:56 / 59
页数:4
相关论文
共 9 条
[1]   Epiluminescence microscopy: Criteria of cutaneous melanoma progression [J].
Argenziano, G ;
Fabbrocini, G ;
Carli, P ;
DeGiorgi, V ;
Delfino, M .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1997, 37 (01) :68-74
[2]  
Blum A, 2003, HAUTARZT, V54, P279, DOI 10.1007/s00105-003-0496-3
[3]   Histopathologic correlation in dermoscopy -: A micropunch technique [J].
Braun, RP ;
Kaya, G ;
Masouyé, I ;
Krischer, J ;
Saurat, JH .
ARCHIVES OF DERMATOLOGY, 2003, 139 (03) :349-351
[4]   In vivo optical coherence tomography imaging of human skin: norm and pathology [J].
Gladkova, ND ;
Petrova, GA ;
Nikulin, NK ;
Radenska-Lopovok, SG ;
Snopova, LB ;
Chumakov, YP ;
Nasonova, VA ;
Gelikonov, VM ;
Gelikonov, GV ;
Kuranov, RV ;
Sergeev, AM ;
Feldchtein, FI .
SKIN RESEARCH AND TECHNOLOGY, 2000, 6 (01) :6-16
[5]  
Soyer HP, 2000, EUR J DERMATOL, V10, P22
[6]   Comparison of high frequency ultrasound and optical coherence tomography as modalities for high resolution and non invasive skin imaging [J].
Vogt, M ;
Knüttel, A ;
Hoffmann, K ;
Altmeyer, P ;
Ermert, H .
BIOMEDIZINISCHE TECHNIK, 2003, 48 (05) :116-121
[7]   Optical coherence tomography in dermatology: a review [J].
Welzel, J .
SKIN RESEARCH AND TECHNOLOGY, 2001, 7 (01) :1-9
[8]   Optical coherence tomography of the human skin [J].
Welzel, J ;
Lankenau, E ;
Birngruber, R ;
Engelhardt, R .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1997, 37 (06) :958-963
[9]   HISTOPATHOLOGIC CORRELATES OF STRUCTURES SEEN ON DERMOSCOPY (EPILUMINESCENCE MICROSCOPY) [J].
YADAV, S ;
VOSSAERT, KA ;
KOPF, AW ;
SILVERMAN, M ;
GRINJORGENSEN, C .
AMERICAN JOURNAL OF DERMATOPATHOLOGY, 1993, 15 (04) :297-305