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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Lentigo maligna &#40;LM&#41;&#44; an in situ lesion&#44; and lentigo maligna melanoma &#40;LMM&#41;&#44; which invades the dermis&#44; constitute a diagnostic and therapeutic challenge&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">Differential diagnosis includes seborrheic keratosis&#44; solar lentigo&#44; lichenoid keratosis&#44; actinic keratosis&#44; and pigmented actinic keratosis&#46; Dermoscopic criteria may assist in the diagnosis of LM and LMM&#44; but lack full sensitivity and specificity&#46; While histologic diagnosis is the gold standard&#44; atypical melanocytes are rare and sparsely distributed in these two conditions&#46; LM is thus difficult to distinguish from melanocytic hyperplasia in photodamaged skin&#44; and lesion margins are hard to define&#46; Some authors have recently highlighted the importance of questioning any histopathological diagnosis of junctional nevus&#44; dysplastic nevus&#44; or atypical lentiginous nevus for lesions occurring in photodamaged skin on the face and neck&#46; Nevi in this area are typically papule-type lesions of the same color as adjoining skin&#44; but are clinically different from LM&#46; Any of the above nevus diagnoses may underestimate an LM lesion as a benign junctional melanocytic proliferation&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">1</span></a> Immunohistochemistry can be of use in these equivocal cases&#46; Typical markers include S-100&#44; human melanoma black-45 antigen &#40;HMB-45&#41;&#44; melan-A &#40;MART-1&#41;&#44; and microphthalmia-associated transcription factor &#40;MITF&#41;&#44; all of which are highly sensitive to melanocytes&#46; However&#44; these markers fail to differentiate melanocytic nevi from melanoma lesions&#59; P16 protein expression and proliferation markers Ki-67 and pHH-3 help with this&#46; Identification of specific mutations in the <span class="elsevierStyleItalic">BRAF</span>&#44; <span class="elsevierStyleItalic">NRAS</span> and <span class="elsevierStyleItalic">KIT</span> genes may be of use&#44; especially given the recent availability of targeted drugs&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">2</span></a></p><p id="par0015" class="elsevierStylePara elsevierViewall">Reflectance confocal microscopy &#40;RCM&#41; was introduced to improve diagnostic accuracy&#44; define the extent of a lesion&#44; and detect recurrences&#46; RCM allows the performance of what might be termed an in vivo optical biopsy with no need for surgery&#46; There is a published diagnostic algorithm with 93&#37; sensitivity and 82&#37; specificity&#44;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">3</span></a> and RCM is particularly useful for distinguishing facial LM from benign pigmented macules without the need for a biopsy&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">4</span></a> Moreover&#44; presurgical mapping may help reduce positive-margin rates and recurrence rates&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">The treatment of choice for LM and LMM is surgical excision&#46; Several authors have indicated that 5-mm margins may be inadequate for LM&#44; particularly owing to amelanotic spread on the periphery of the lesion&#59; 9-mm resection margins are recommended instead&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">5</span></a> Mohs micrographic surgery is more precise than excision and has a lower recurrence rate &#40;0&#37;-6&#46;25&#37;&#41;&#46; Certain cases may be selected for second-line treatments such as imiquimod&#44; radiotherapy&#44; and cryosurgery&#46; A review of radiotherapy for LM found a recurrence rate of 5&#37; and a rate of only 1&#46;4&#37; for progression to LMM&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">6</span></a> The authors recommend mapping the lesion first with RCM and irradiating the lesion area plus a 1-cm margin of healthy skin at a depth of 5<span class="elsevierStyleHsp" style=""></span>mm to ensure irradiation of hair follicle melanocytes&#46; They highlight the presence of blue-gray pigmentation after treatment and the fact that RCM can distinguish this coloring from persistent or recurrent LM&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">Developing a familiarity with new imaging techniques and therapeutic options for LM and LMM is important in order to offer our patients greater diagnostic accuracy and appropriate treatments&#44; and to meet current growing demand for noninvasive&#44; cosmetically acceptable techniques&#46;</p></span>"
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Resident's Forum
Diagnostic and Therapeutic Techniques in Lentigo Maligna: An Update
FR-Lentigo maligno, actualización en técnicas diagnósticas y terapéuticas
H. Collgros
Autor para correspondencia
helenacollgros@gmail.com

Corresponding author.
, N. Lamas-Doménech
Departamento de Dermatología, Hospital Universitari Sagrat Cor, Barcelona, Spain
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Lentigo maligna &#40;LM&#41;&#44; an in situ lesion&#44; and lentigo maligna melanoma &#40;LMM&#41;&#44; which invades the dermis&#44; constitute a diagnostic and therapeutic challenge&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">Differential diagnosis includes seborrheic keratosis&#44; solar lentigo&#44; lichenoid keratosis&#44; actinic keratosis&#44; and pigmented actinic keratosis&#46; Dermoscopic criteria may assist in the diagnosis of LM and LMM&#44; but lack full sensitivity and specificity&#46; While histologic diagnosis is the gold standard&#44; atypical melanocytes are rare and sparsely distributed in these two conditions&#46; LM is thus difficult to distinguish from melanocytic hyperplasia in photodamaged skin&#44; and lesion margins are hard to define&#46; Some authors have recently highlighted the importance of questioning any histopathological diagnosis of junctional nevus&#44; dysplastic nevus&#44; or atypical lentiginous nevus for lesions occurring in photodamaged skin on the face and neck&#46; Nevi in this area are typically papule-type lesions of the same color as adjoining skin&#44; but are clinically different from LM&#46; Any of the above nevus diagnoses may underestimate an LM lesion as a benign junctional melanocytic proliferation&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">1</span></a> Immunohistochemistry can be of use in these equivocal cases&#46; Typical markers include S-100&#44; human melanoma black-45 antigen &#40;HMB-45&#41;&#44; melan-A &#40;MART-1&#41;&#44; and microphthalmia-associated transcription factor &#40;MITF&#41;&#44; all of which are highly sensitive to melanocytes&#46; However&#44; these markers fail to differentiate melanocytic nevi from melanoma lesions&#59; P16 protein expression and proliferation markers Ki-67 and pHH-3 help with this&#46; Identification of specific mutations in the <span class="elsevierStyleItalic">BRAF</span>&#44; <span class="elsevierStyleItalic">NRAS</span> and <span class="elsevierStyleItalic">KIT</span> genes may be of use&#44; especially given the recent availability of targeted drugs&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">2</span></a></p><p id="par0015" class="elsevierStylePara elsevierViewall">Reflectance confocal microscopy &#40;RCM&#41; was introduced to improve diagnostic accuracy&#44; define the extent of a lesion&#44; and detect recurrences&#46; RCM allows the performance of what might be termed an in vivo optical biopsy with no need for surgery&#46; There is a published diagnostic algorithm with 93&#37; sensitivity and 82&#37; specificity&#44;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">3</span></a> and RCM is particularly useful for distinguishing facial LM from benign pigmented macules without the need for a biopsy&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">4</span></a> Moreover&#44; presurgical mapping may help reduce positive-margin rates and recurrence rates&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">The treatment of choice for LM and LMM is surgical excision&#46; Several authors have indicated that 5-mm margins may be inadequate for LM&#44; particularly owing to amelanotic spread on the periphery of the lesion&#59; 9-mm resection margins are recommended instead&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">5</span></a> Mohs micrographic surgery is more precise than excision and has a lower recurrence rate &#40;0&#37;-6&#46;25&#37;&#41;&#46; Certain cases may be selected for second-line treatments such as imiquimod&#44; radiotherapy&#44; and cryosurgery&#46; A review of radiotherapy for LM found a recurrence rate of 5&#37; and a rate of only 1&#46;4&#37; for progression to LMM&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">6</span></a> The authors recommend mapping the lesion first with RCM and irradiating the lesion area plus a 1-cm margin of healthy skin at a depth of 5<span class="elsevierStyleHsp" style=""></span>mm to ensure irradiation of hair follicle melanocytes&#46; They highlight the presence of blue-gray pigmentation after treatment and the fact that RCM can distinguish this coloring from persistent or recurrent LM&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">Developing a familiarity with new imaging techniques and therapeutic options for LM and LMM is important in order to offer our patients greater diagnostic accuracy and appropriate treatments&#44; and to meet current growing demand for noninvasive&#44; cosmetically acceptable techniques&#46;</p></span>"
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