FREQUENCY AND MORPHOLOGIC CHARACTERISTICS OF INVASIVE MELANOMAS LACKING SPECIFIC SURFACE MICROSCOPIC FEATURES

Citation
Sw. Menzies et al., FREQUENCY AND MORPHOLOGIC CHARACTERISTICS OF INVASIVE MELANOMAS LACKING SPECIFIC SURFACE MICROSCOPIC FEATURES, Archives of dermatology, 132(10), 1996, pp. 1178-1182
Citations number
20
Categorie Soggetti
Dermatology & Venereal Diseases
Journal title
ISSN journal
0003987X
Volume
132
Issue
10
Year of publication
1996
Pages
1178 - 1182
Database
ISI
SICI code
0003-987X(1996)132:10<1178:FAMCOI>2.0.ZU;2-L
Abstract
Objectives: To create a simple diagnostic method for invasive melanoma with in vivo cutaneous surface microscopy (epiluminescence microscopy , dermoscopy, dermatoscopy) and to analyze the incidence and character istics of those invasive melanomas that had no diagnostic features by means of hand-held surface microscopes. Design: Pigmented skin lesions were photographed in vivo with the use of immersion oil. All were exc ised and reviewed for histological diagnosis. A training set of 62 inv asive melanomas and 159 atypical nonmelanomas and a test set of 45 inv asive melanomas and 119 atypical nonmelanomas were used. Images from t he training set were scored for 72 surface microscopic features. Those features with a low sensitivity (0%) and high specificity (>85%) were used to create a simple diagnostic model for invasive melanoma. Setti ng: All patients were recruited from the Sydney (Australia) Melanoma U nit (a primary case and referral center). Patients: A random sample of patients whose lesions were excised, selected from a larger database. Main Outcome Measures: Sensitivity and specificity of the model for d iagnosis of invasive melanona. Results: The model gave a sensitivity o f 92% (98/107) and specificity of 71%. Of the 9 ''featureless'' melano mas the model failed to detect, 6 were pigmented and thin and had a pi gment network. The other 3 were thicker, hypomelanotic lesions lacking a pigment network, some with prominent telangiectases, and all with o nly small areas of pigment. All featureless melanomas noted by the pat ients had a history of change in color, shape, or size. Conclusions: S urface microscopy does not allow 100% sensitivity in diagnosing invasi ve melanoma and therefore cannot be used as the sole indicator for exc ision. Clinical history is an important consideration when featureless lesions are diagnosed.