Negative pigment network: An additional dermoscopic feature for the diagnosis of melanoma

被引:36
作者
Pizzichetta, Maria A. [1 ]
Talamini, Renato [1 ]
Marghoob, Ash A. [2 ]
Soyer, H. Peter [3 ]
Argenziano, Giuseppe [4 ]
Bono, Riccardo [5 ]
Corradin, M. Teresa [6 ]
De Giorgi, Vincenzo [7 ]
Gonzalez, Marian A. [8 ]
Kolm, Isabel [9 ]
Kopf, Andrew W. [10 ]
Malvehy, Joseph [11 ]
Nami, Niccolo [12 ]
Oliviero, Margaret [9 ]
Pellacani, Giovanni [13 ]
Puig, Susana [11 ]
Rabinovitz, Harold [9 ]
Rubegni, Pietro [12 ]
Seidenari, Stefania [13 ]
Stanganelli, Ignazio [14 ]
Veronesi, Andrea [1 ]
Zalaudek, Iris [15 ]
Zampieri, Pierfrancesco [8 ]
Menzies, Scott W. [16 ,17 ]
机构
[1] Natl Canc Inst, Ctr Riferimento Oncol, Aviano, Italy
[2] Mem Sloan Kettering Canc Ctr, Dermatol Sect, New York, NY 10021 USA
[3] Univ Queensland, Sch Med, Princess Alexandra Hosp, Dermatol Res Ctr, Brisbane, Qld, Australia
[4] IRCCS, Arcispedale Santa Maria Nuova, Dermatol & Skin Canc Unit, Reggio Emilia, Italy
[5] IRCCS, Ist Dermopat Immacolata, Rome, Italy
[6] Pordenone Hosp, Div Dermatol, Pordenone, Italy
[7] Univ Florence, Dept Dermatol, I-50121 Florence, Italy
[8] Merano Hosp, Div Dermatol, Merano, Italy
[9] Univ Miami, Dept Dermatol, Coral Gables, FL 33124 USA
[10] NYU, Sch Med, New York, NY 10003 USA
[11] Inst Invest Biomed August Pi & Sunyer, Hosp Clin, Dept Dermatol, Melanoma Unit, Barcelona, Spain
[12] Univ Siena, Dept Dermatol, I-53100 Siena, Italy
[13] Univ Modena & Reggio Emilia, Dept Dermatol, Modena, Italy
[14] Ist Tumori Romagna, Skin Canc Unit, Meldola, Italy
[15] Med Univ Graz, Graz, Austria
[16] Univ Sydney, Royal Prince Alfred Hosp, Sydney Melanoma Diagnost Ctr, Sydney, NSW 2006, Australia
[17] Univ Sydney, Discipline Dermatol, Sydney, NSW 2006, Australia
关键词
dermoscopy; histiocytoma; melanocytic nevus; melanoma; negative pigment network; Spitz nevus; POLARIZED DERMOSCOPY; SKIN-LESIONS; SPITZ NEVI; MICROSCOPY;
D O I
10.1016/j.jaad.2012.08.012
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: The negative pigment network (NPN) is seen as a negative of the pigmented network and it is purported to be a melanoma-specific structure. Objectives: We sought to assess the frequency, sensitivity, specificity, and odds ratios (ORs) of NPN between melanoma cases and a group of control lesions. Methods: Digitalized images of skin lesions from 679 patients with histopathological diagnosis of dermatofibroma (115), melanocytic nevus (220), Spitz nevus (139), and melanoma (205) were retrospectively collected and blindly evaluated to assess the presence/absence of NPN. Results: The frequency of occurrence of NPN was higher in the melanoma group (34.6%) than in Spitz nevus (28.8%), melanocytic nevus (18.2%), and dermatofibroma (11.3%) groups. An OR of 1.8 emerged for the diagnosis of melanoma in the presence of NPN as compared with nonmelanoma diagnosis. Conversely, for melanocytic nevi and dermatofibromas the OR was very low (0.5 and 0.3, respectively). For Spitz nevi the OR of 1.1 was not statistically significant. When comparing melanoma with dermatofibroma, melanocytic nevus, and Spitz nevus, we observed a significantly higher frequency of multicomponent pattern (68.1%), asymmetric pigmentation (92.9%), irregularly distributed NPN (87.3%), and peripheral location of NPN (66.2%) in melanomas. Limitations: Further studies can provide the precise dermoscopic-histopathologic correlation of NPN in melanoma and other lesions. Conclusions: The overall morphologic pattern of NPN, such as the irregular distribution and the peripheral location of NPN, along with the multicomponent pattern and the asymmetric pigmentation could be used as additional features in distinguishing melanoma from Spitz nevus and other benign lesions. (J Am Acad Dermatol 2013;68:552-9.)
引用
收藏
页码:552 / 559
页数:8
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