Nonmelanocytic Lesions Defying the Two-Step Dermoscopy Algorithm
The first step of the two-step algorithm of dermoscopy aims at differentiating melanocytic from nonmelanocytic pigmented lesions, using a stepwise evaluation for the presence of specific dermoscopic criteria. The purpose of this article is to heighten awareness of clinicians to nonmelanocytic lesion...
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Veröffentlicht in: | Dermatologic surgery 2006-11, Vol.32 (11), p.1398-1406 |
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description | The first step of the two-step algorithm of dermoscopy aims at differentiating melanocytic from nonmelanocytic pigmented lesions, using a stepwise evaluation for the presence of specific dermoscopic criteria. The purpose of this article is to heighten awareness of clinicians to nonmelanocytic lesions that defy the two-step algorithm, thus simulating melanocytic lesions dermoscopically. Seborrheic keratosis, solar lentigo, dermatofibroma, and supernumerary accessory nipple may present with network-like structures. Seborrheic keratosis, dermatofibroma, subcorneal hemorrhage, basal cell carcinoma (BCC), and cutaneous metastases of breast and other cancers may contain pigmented globules. Peripheral streaks can also be seen in seborrheic keratosis and BCC. Homogenous bluish pigmentation, simulating a blue nevus, can also be seen in benign vascular lesions, Kaposi sarcoma, radiation tattoo, and BCC. This overlap of features between melanocytic and nonmelanocytic lesions suggests that integration of all dermoscopic features in the lesion, rather than a stepwise evaluation, may facilitate reaching the correct diagnosis in select cases as outlined in this article. |
doi_str_mv | 10.1097/00042728-200611000-00014 |
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The purpose of this article is to heighten awareness of clinicians to nonmelanocytic lesions that defy the two-step algorithm, thus simulating melanocytic lesions dermoscopically. Seborrheic keratosis, solar lentigo, dermatofibroma, and supernumerary accessory nipple may present with network-like structures. Seborrheic keratosis, dermatofibroma, subcorneal hemorrhage, basal cell carcinoma (BCC), and cutaneous metastases of breast and other cancers may contain pigmented globules. Peripheral streaks can also be seen in seborrheic keratosis and BCC. Homogenous bluish pigmentation, simulating a blue nevus, can also be seen in benign vascular lesions, Kaposi sarcoma, radiation tattoo, and BCC. This overlap of features between melanocytic and nonmelanocytic lesions suggests that integration of all dermoscopic features in the lesion, rather than a stepwise evaluation, may facilitate reaching the correct diagnosis in select cases as outlined in this article.</description><identifier>ISSN: 1076-0512</identifier><identifier>EISSN: 1524-4725</identifier><identifier>DOI: 10.1097/00042728-200611000-00014</identifier><identifier>PMID: 17083595</identifier><language>eng</language><publisher>Malden, MA: by the American Society for Dermatologic Surgery, Inc</publisher><subject>Algorithms ; Biological and medical sciences ; Decision Trees ; Dermatology ; Dermoscopy - methods ; Humans ; Medical sciences ; Melanoma, Amelanotic - diagnosis ; Melanoma, Amelanotic - pathology ; Nevus - diagnosis ; Nevus - pathology ; Predictive Value of Tests ; Skin Neoplasms - diagnosis ; Skin Neoplasms - pathology ; Skin plastic surgery ; Surgery (general aspects). Transplantations, organ and tissue grafts. 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The purpose of this article is to heighten awareness of clinicians to nonmelanocytic lesions that defy the two-step algorithm, thus simulating melanocytic lesions dermoscopically. Seborrheic keratosis, solar lentigo, dermatofibroma, and supernumerary accessory nipple may present with network-like structures. Seborrheic keratosis, dermatofibroma, subcorneal hemorrhage, basal cell carcinoma (BCC), and cutaneous metastases of breast and other cancers may contain pigmented globules. Peripheral streaks can also be seen in seborrheic keratosis and BCC. Homogenous bluish pigmentation, simulating a blue nevus, can also be seen in benign vascular lesions, Kaposi sarcoma, radiation tattoo, and BCC. This overlap of features between melanocytic and nonmelanocytic lesions suggests that integration of all dermoscopic features in the lesion, rather than a stepwise evaluation, may facilitate reaching the correct diagnosis in select cases as outlined in this article.</description><subject>Algorithms</subject><subject>Biological and medical sciences</subject><subject>Decision Trees</subject><subject>Dermatology</subject><subject>Dermoscopy - methods</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Melanoma, Amelanotic - diagnosis</subject><subject>Melanoma, Amelanotic - pathology</subject><subject>Nevus - diagnosis</subject><subject>Nevus - pathology</subject><subject>Predictive Value of Tests</subject><subject>Skin Neoplasms - diagnosis</subject><subject>Skin Neoplasms - pathology</subject><subject>Skin plastic surgery</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. 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Transplantations, organ and tissue grafts. Graft diseases</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SCOPE, ALON</creatorcontrib><creatorcontrib>BENVENUTO-ANDRADE, CRISTIANE</creatorcontrib><creatorcontrib>AGERO, ANNA LIZA C</creatorcontrib><creatorcontrib>MARGHOOB, ASHFAQ A</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Dermatologic surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SCOPE, ALON</au><au>BENVENUTO-ANDRADE, CRISTIANE</au><au>AGERO, ANNA LIZA C</au><au>MARGHOOB, ASHFAQ A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nonmelanocytic Lesions Defying the Two-Step Dermoscopy Algorithm</atitle><jtitle>Dermatologic surgery</jtitle><addtitle>Dermatol Surg</addtitle><date>2006-11</date><risdate>2006</risdate><volume>32</volume><issue>11</issue><spage>1398</spage><epage>1406</epage><pages>1398-1406</pages><issn>1076-0512</issn><eissn>1524-4725</eissn><abstract>The first step of the two-step algorithm of dermoscopy aims at differentiating melanocytic from nonmelanocytic pigmented lesions, using a stepwise evaluation for the presence of specific dermoscopic criteria. The purpose of this article is to heighten awareness of clinicians to nonmelanocytic lesions that defy the two-step algorithm, thus simulating melanocytic lesions dermoscopically. Seborrheic keratosis, solar lentigo, dermatofibroma, and supernumerary accessory nipple may present with network-like structures. Seborrheic keratosis, dermatofibroma, subcorneal hemorrhage, basal cell carcinoma (BCC), and cutaneous metastases of breast and other cancers may contain pigmented globules. Peripheral streaks can also be seen in seborrheic keratosis and BCC. Homogenous bluish pigmentation, simulating a blue nevus, can also be seen in benign vascular lesions, Kaposi sarcoma, radiation tattoo, and BCC. This overlap of features between melanocytic and nonmelanocytic lesions suggests that integration of all dermoscopic features in the lesion, rather than a stepwise evaluation, may facilitate reaching the correct diagnosis in select cases as outlined in this article.</abstract><cop>Malden, MA</cop><pub>by the American Society for Dermatologic Surgery, Inc</pub><pmid>17083595</pmid><doi>10.1097/00042728-200611000-00014</doi><tpages>9</tpages></addata></record> |
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subjects | Algorithms Biological and medical sciences Decision Trees Dermatology Dermoscopy - methods Humans Medical sciences Melanoma, Amelanotic - diagnosis Melanoma, Amelanotic - pathology Nevus - diagnosis Nevus - pathology Predictive Value of Tests Skin Neoplasms - diagnosis Skin Neoplasms - pathology Skin plastic surgery Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases |
title | Nonmelanocytic Lesions Defying the Two-Step Dermoscopy Algorithm |
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