Atypical Spitzoid Melanocytic Tumors With Positive Sentinel Lymph Nodes in Children and Teenagers, and Comparison With Histologically Unambiguous and Lethal Melanomas
Children and teenagers with a positive sentinel lymph node (SLN) after a prior diagnosis of an atypical spitzoid melanocytic tumor (ASMT) are usually cared for clinically in the same way as patients with melanoma. Little is known about long-term follow-up of these individuals to determine whether th...
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creator | BUSAM, Klaus J MURALI, Rajmohan KAYTON, Marc LAQUAGLIA, Michael SCOLYER, Richard A PULITZER, Melissa MCCARTHY, Stanley W THOMPSON, John F SHAW, Helen M BRADY, Mary S COIT, Daniel G DUSZA, Stephen WILMOTT, James |
description | Children and teenagers with a positive sentinel lymph node (SLN) after a prior diagnosis of an atypical spitzoid melanocytic tumor (ASMT) are usually cared for clinically in the same way as patients with melanoma. Little is known about long-term follow-up of these individuals to determine whether this practice is appropriate. To learn more about the biology of these tumors we retrospectively reviewed the clinical and pathologic findings of children and teenagers ( |
doi_str_mv | 10.1097/PAS.0b013e3181ac1927 |
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Little is known about long-term follow-up of these individuals to determine whether this practice is appropriate. To learn more about the biology of these tumors we retrospectively reviewed the clinical and pathologic findings of children and teenagers (<18 y of age at the time of diagnosis) with an ASMT, positive SLN and follow-up of at least 3 years. Their findings were compared with histologically unambiguous melanomas of children or teenagers, who had a positive SLN or died of metastatic melanoma. Eleven individuals, 6 girls and 5 boys, with primary ASMT and positive SLN were identified. The primary tumors ranged in thickness from 2.1 to 12 mm (median, 4.6 mm; mean, 5 mm). The tumor mitotic rate ranged from 1 to 10 mitoses/mm (median, 3/mm, median, 3/mm). The positive SLNs included 6 nodes with intranodal melanocytic aggregates measuring <1 mm in greatest dimension, and 5 nodes, in which the size of the melanocyte deposits was >/=1 mm. All the patients with ASMT and positive SLN remained free of disease with a median follow-up of 47 months (mean, 61 mo, range: 36 to 132 mo). In contrast, 2 of 5 patients <18 years of age with a histologically unambiguous melanoma and a positive SLN died of metastatic melanoma. The overall disease-specific mortality rate for all patients <18 years of age diagnosed with melanoma was 12%. Our findings confirm that children and teenagers with ASMTs and positive SLNs have a less aggressive clinical course than those with histologically unambiguous melanoma.</description><identifier>ISSN: 0147-5185</identifier><identifier>EISSN: 1532-0979</identifier><identifier>DOI: 10.1097/PAS.0b013e3181ac1927</identifier><identifier>PMID: 19609204</identifier><identifier>CODEN: AJSPDX</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>Adolescent ; Biological and medical sciences ; Child ; Dermatology ; Disease-Free Survival ; Female ; Hematologic and hematopoietic diseases ; Humans ; Investigative techniques, diagnostic techniques (general aspects) ; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis ; Male ; Medical sciences ; Melanoma - secondary ; Melanoma - surgery ; Nevus, Epithelioid and Spindle Cell - pathology ; Nevus, Epithelioid and Spindle Cell - surgery ; Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques ; Sentinel Lymph Node Biopsy ; Skin Neoplasms - pathology ; Skin Neoplasms - surgery ; Tumors of the skin and soft tissue. Premalignant lesions</subject><ispartof>The American journal of surgical pathology, 2009-09, Vol.33 (9), p.1386-1395</ispartof><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c335t-45c6ca7ff41626c415a75cf7c45e4bf7a6fab360c90d81c35825abe1e1fb85383</citedby><cites>FETCH-LOGICAL-c335t-45c6ca7ff41626c415a75cf7c45e4bf7a6fab360c90d81c35825abe1e1fb85383</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21878577$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19609204$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>BUSAM, Klaus J</creatorcontrib><creatorcontrib>MURALI, Rajmohan</creatorcontrib><creatorcontrib>KAYTON, Marc</creatorcontrib><creatorcontrib>LAQUAGLIA, Michael</creatorcontrib><creatorcontrib>SCOLYER, Richard A</creatorcontrib><creatorcontrib>PULITZER, Melissa</creatorcontrib><creatorcontrib>MCCARTHY, Stanley W</creatorcontrib><creatorcontrib>THOMPSON, John F</creatorcontrib><creatorcontrib>SHAW, Helen M</creatorcontrib><creatorcontrib>BRADY, Mary S</creatorcontrib><creatorcontrib>COIT, Daniel G</creatorcontrib><creatorcontrib>DUSZA, Stephen</creatorcontrib><creatorcontrib>WILMOTT, James</creatorcontrib><title>Atypical Spitzoid Melanocytic Tumors With Positive Sentinel Lymph Nodes in Children and Teenagers, and Comparison With Histologically Unambiguous and Lethal Melanomas</title><title>The American journal of surgical pathology</title><addtitle>Am J Surg Pathol</addtitle><description>Children and teenagers with a positive sentinel lymph node (SLN) after a prior diagnosis of an atypical spitzoid melanocytic tumor (ASMT) are usually cared for clinically in the same way as patients with melanoma. Little is known about long-term follow-up of these individuals to determine whether this practice is appropriate. To learn more about the biology of these tumors we retrospectively reviewed the clinical and pathologic findings of children and teenagers (<18 y of age at the time of diagnosis) with an ASMT, positive SLN and follow-up of at least 3 years. Their findings were compared with histologically unambiguous melanomas of children or teenagers, who had a positive SLN or died of metastatic melanoma. Eleven individuals, 6 girls and 5 boys, with primary ASMT and positive SLN were identified. The primary tumors ranged in thickness from 2.1 to 12 mm (median, 4.6 mm; mean, 5 mm). The tumor mitotic rate ranged from 1 to 10 mitoses/mm (median, 3/mm, median, 3/mm). The positive SLNs included 6 nodes with intranodal melanocytic aggregates measuring <1 mm in greatest dimension, and 5 nodes, in which the size of the melanocyte deposits was >/=1 mm. All the patients with ASMT and positive SLN remained free of disease with a median follow-up of 47 months (mean, 61 mo, range: 36 to 132 mo). In contrast, 2 of 5 patients <18 years of age with a histologically unambiguous melanoma and a positive SLN died of metastatic melanoma. The overall disease-specific mortality rate for all patients <18 years of age diagnosed with melanoma was 12%. Our findings confirm that children and teenagers with ASMTs and positive SLNs have a less aggressive clinical course than those with histologically unambiguous melanoma.</description><subject>Adolescent</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Dermatology</subject><subject>Disease-Free Survival</subject><subject>Female</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Humans</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Melanoma - secondary</subject><subject>Melanoma - surgery</subject><subject>Nevus, Epithelioid and Spindle Cell - pathology</subject><subject>Nevus, Epithelioid and Spindle Cell - surgery</subject><subject>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</subject><subject>Sentinel Lymph Node Biopsy</subject><subject>Skin Neoplasms - pathology</subject><subject>Skin Neoplasms - surgery</subject><subject>Tumors of the skin and soft tissue. Premalignant lesions</subject><issn>0147-5185</issn><issn>1532-0979</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkcFu1DAQhi0EokvhDRDyBU6keOw4To6rFbRIC1TarThGjjPZNUrsYDtI6QPxnKTdFUicRqP55p9f8xPyGtgVsEp9uF3vrljDQKCAErSBiqsnZAVS8GyZV0_JikGuMgmlvCAvYvzBGPAS-HNyAVXBKs7yFfm9TvNoje7pbrTp3tuWfsFeO2_mZA3dT4MPkX636UhvfbTJ_kK6Q5esw55u52E80q--xUito5uj7duAjmrX0j2i0wcM8f1ju_HDqION3p3EbmxMvveHh9P9TO-cHhp7mPwUH_EtpuPi6WRl0PEledbpPuKrc70kd58-7jc32fbb9efNepsZIWTKcmkKo1XX5VDwwuQgtZKmUyaXmDed0kWnG1EwU7G2BCNkyaVuEBC6ppSiFJfk3Ul3DP7nhDHVg40G-8UGLt7qQhUgKi4XMD-BJvgYA3b1GOygw1wDqx_yqZd86v_zWdbenPWnZsD239I5kAV4ewZ0XF7TBe2MjX85DqUqpVLiD6FSnXc</recordid><startdate>20090901</startdate><enddate>20090901</enddate><creator>BUSAM, Klaus J</creator><creator>MURALI, Rajmohan</creator><creator>KAYTON, Marc</creator><creator>LAQUAGLIA, Michael</creator><creator>SCOLYER, Richard A</creator><creator>PULITZER, Melissa</creator><creator>MCCARTHY, Stanley W</creator><creator>THOMPSON, John F</creator><creator>SHAW, Helen M</creator><creator>BRADY, Mary S</creator><creator>COIT, Daniel G</creator><creator>DUSZA, Stephen</creator><creator>WILMOTT, James</creator><general>Lippincott Williams & Wilkins</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20090901</creationdate><title>Atypical Spitzoid Melanocytic Tumors With Positive Sentinel Lymph Nodes in Children and Teenagers, and Comparison With Histologically Unambiguous and Lethal Melanomas</title><author>BUSAM, Klaus J ; MURALI, Rajmohan ; KAYTON, Marc ; LAQUAGLIA, Michael ; SCOLYER, Richard A ; PULITZER, Melissa ; MCCARTHY, Stanley W ; THOMPSON, John F ; SHAW, Helen M ; BRADY, Mary S ; COIT, Daniel G ; DUSZA, Stephen ; WILMOTT, James</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c335t-45c6ca7ff41626c415a75cf7c45e4bf7a6fab360c90d81c35825abe1e1fb85383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adolescent</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Dermatology</topic><topic>Disease-Free Survival</topic><topic>Female</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Humans</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Melanoma - secondary</topic><topic>Melanoma - surgery</topic><topic>Nevus, Epithelioid and Spindle Cell - pathology</topic><topic>Nevus, Epithelioid and Spindle Cell - surgery</topic><topic>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</topic><topic>Sentinel Lymph Node Biopsy</topic><topic>Skin Neoplasms - pathology</topic><topic>Skin Neoplasms - surgery</topic><topic>Tumors of the skin and soft tissue. Premalignant lesions</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>BUSAM, Klaus J</creatorcontrib><creatorcontrib>MURALI, Rajmohan</creatorcontrib><creatorcontrib>KAYTON, Marc</creatorcontrib><creatorcontrib>LAQUAGLIA, Michael</creatorcontrib><creatorcontrib>SCOLYER, Richard A</creatorcontrib><creatorcontrib>PULITZER, Melissa</creatorcontrib><creatorcontrib>MCCARTHY, Stanley W</creatorcontrib><creatorcontrib>THOMPSON, John F</creatorcontrib><creatorcontrib>SHAW, Helen M</creatorcontrib><creatorcontrib>BRADY, Mary S</creatorcontrib><creatorcontrib>COIT, Daniel G</creatorcontrib><creatorcontrib>DUSZA, Stephen</creatorcontrib><creatorcontrib>WILMOTT, James</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>The American journal of surgical pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>BUSAM, Klaus J</au><au>MURALI, Rajmohan</au><au>KAYTON, Marc</au><au>LAQUAGLIA, Michael</au><au>SCOLYER, Richard A</au><au>PULITZER, Melissa</au><au>MCCARTHY, Stanley W</au><au>THOMPSON, John F</au><au>SHAW, Helen M</au><au>BRADY, Mary S</au><au>COIT, Daniel G</au><au>DUSZA, Stephen</au><au>WILMOTT, James</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Atypical Spitzoid Melanocytic Tumors With Positive Sentinel Lymph Nodes in Children and Teenagers, and Comparison With Histologically Unambiguous and Lethal Melanomas</atitle><jtitle>The American journal of surgical pathology</jtitle><addtitle>Am J Surg Pathol</addtitle><date>2009-09-01</date><risdate>2009</risdate><volume>33</volume><issue>9</issue><spage>1386</spage><epage>1395</epage><pages>1386-1395</pages><issn>0147-5185</issn><eissn>1532-0979</eissn><coden>AJSPDX</coden><abstract>Children and teenagers with a positive sentinel lymph node (SLN) after a prior diagnosis of an atypical spitzoid melanocytic tumor (ASMT) are usually cared for clinically in the same way as patients with melanoma. Little is known about long-term follow-up of these individuals to determine whether this practice is appropriate. To learn more about the biology of these tumors we retrospectively reviewed the clinical and pathologic findings of children and teenagers (<18 y of age at the time of diagnosis) with an ASMT, positive SLN and follow-up of at least 3 years. Their findings were compared with histologically unambiguous melanomas of children or teenagers, who had a positive SLN or died of metastatic melanoma. Eleven individuals, 6 girls and 5 boys, with primary ASMT and positive SLN were identified. The primary tumors ranged in thickness from 2.1 to 12 mm (median, 4.6 mm; mean, 5 mm). The tumor mitotic rate ranged from 1 to 10 mitoses/mm (median, 3/mm, median, 3/mm). The positive SLNs included 6 nodes with intranodal melanocytic aggregates measuring <1 mm in greatest dimension, and 5 nodes, in which the size of the melanocyte deposits was >/=1 mm. All the patients with ASMT and positive SLN remained free of disease with a median follow-up of 47 months (mean, 61 mo, range: 36 to 132 mo). In contrast, 2 of 5 patients <18 years of age with a histologically unambiguous melanoma and a positive SLN died of metastatic melanoma. The overall disease-specific mortality rate for all patients <18 years of age diagnosed with melanoma was 12%. Our findings confirm that children and teenagers with ASMTs and positive SLNs have a less aggressive clinical course than those with histologically unambiguous melanoma.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins</pub><pmid>19609204</pmid><doi>10.1097/PAS.0b013e3181ac1927</doi><tpages>10</tpages></addata></record> |
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subjects | Adolescent Biological and medical sciences Child Dermatology Disease-Free Survival Female Hematologic and hematopoietic diseases Humans Investigative techniques, diagnostic techniques (general aspects) Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis Male Medical sciences Melanoma - secondary Melanoma - surgery Nevus, Epithelioid and Spindle Cell - pathology Nevus, Epithelioid and Spindle Cell - surgery Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques Sentinel Lymph Node Biopsy Skin Neoplasms - pathology Skin Neoplasms - surgery Tumors of the skin and soft tissue. Premalignant lesions |
title | Atypical Spitzoid Melanocytic Tumors With Positive Sentinel Lymph Nodes in Children and Teenagers, and Comparison With Histologically Unambiguous and Lethal Melanomas |
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