Idiosyncrasies of Scalp Melanoma

Objectives/Hypothesis: Examine the accuracy of sentinel lymph node biopsy (SNB) in scalp melanoma (SM), patterns of nodal metastases, patient outcomes, and the utility of immunohistochemistry (IHC) in SNB evaluation. Study Design: Retrospective. Methods: There were 22 patients, 4 females and 18 male...

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Veröffentlicht in:The Laryngoscope 2007-08, Vol.117 (8), p.1354-1358
Hauptverfasser: Rigual, Nestor R., Cheney, Richard T., Iwenofu, Obiajulu H., Li, Qiang, Loree, Thom R., Popat, Saurin R., Merzianu, Mihai
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container_end_page 1358
container_issue 8
container_start_page 1354
container_title The Laryngoscope
container_volume 117
creator Rigual, Nestor R.
Cheney, Richard T.
Iwenofu, Obiajulu H.
Li, Qiang
Loree, Thom R.
Popat, Saurin R.
Merzianu, Mihai
description Objectives/Hypothesis: Examine the accuracy of sentinel lymph node biopsy (SNB) in scalp melanoma (SM), patterns of nodal metastases, patient outcomes, and the utility of immunohistochemistry (IHC) in SNB evaluation. Study Design: Retrospective. Methods: There were 22 patients, 4 females and 18 males. Sentinel lymph nodes (SLN) were localized via preoperative lymphoscintigraphy, intraoperative gamma probe, and Lymphazurin injection. SLNs were stained with hematoxylin‐eosin, S‐100, HMB‐45, Melan‐A, micropthalmia transcription factor, and tyrosinase. SLNs were grouped into cervical (levels 1–5) and extracervical (parotid, suboccipital, retroauricular) regions. Results: There were 13 posterior and 9 anterior SMs. The first SNB were mapped to the extracervical regions in 77% of posterior and 78% of anterior lesions. SLN number ranged from 1 to 5. Ten patients had positive SLNs (PSLN). Forty percent of the PSLN group had SLNs mapped in both cervical and extracervical sites. Six underwent completion lymphadenectomy, with no additional positive nodes identified. No significant difference between PSLN and negative sentinel node (NSLN) patients was seen when compared by SLN number, Breslow's thickness, tumor ulceration, and clinical outcomes. Mean follow‐up was 35 months. One patient died of disease. One isolated regional recurrence occurred. Sixty percent of PSLN and 92% of NSLN patients were recurrence free at last follow‐up. One distant metastasis occurred in the NSLN group, and one local, one regional, and two patients with distant metastases were in the PSLN group at the time of last follow‐up. Additional IHC did not detect other metastases in the NSLN group. Conclusions: SM is aggressive, as demonstrated by the high rate of SLN metastases, and there were no significant histopathologic factors in the primary tumor that predicted the presence of SLN metastases. SNB was accurate. The majority of first SLNs were localized in extracervical basins.
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Study Design: Retrospective. Methods: There were 22 patients, 4 females and 18 males. Sentinel lymph nodes (SLN) were localized via preoperative lymphoscintigraphy, intraoperative gamma probe, and Lymphazurin injection. SLNs were stained with hematoxylin‐eosin, S‐100, HMB‐45, Melan‐A, micropthalmia transcription factor, and tyrosinase. SLNs were grouped into cervical (levels 1–5) and extracervical (parotid, suboccipital, retroauricular) regions. Results: There were 13 posterior and 9 anterior SMs. The first SNB were mapped to the extracervical regions in 77% of posterior and 78% of anterior lesions. SLN number ranged from 1 to 5. Ten patients had positive SLNs (PSLN). Forty percent of the PSLN group had SLNs mapped in both cervical and extracervical sites. Six underwent completion lymphadenectomy, with no additional positive nodes identified. No significant difference between PSLN and negative sentinel node (NSLN) patients was seen when compared by SLN number, Breslow's thickness, tumor ulceration, and clinical outcomes. Mean follow‐up was 35 months. One patient died of disease. One isolated regional recurrence occurred. Sixty percent of PSLN and 92% of NSLN patients were recurrence free at last follow‐up. One distant metastasis occurred in the NSLN group, and one local, one regional, and two patients with distant metastases were in the PSLN group at the time of last follow‐up. Additional IHC did not detect other metastases in the NSLN group. Conclusions: SM is aggressive, as demonstrated by the high rate of SLN metastases, and there were no significant histopathologic factors in the primary tumor that predicted the presence of SLN metastases. SNB was accurate. The majority of first SLNs were localized in extracervical basins.</description><identifier>ISSN: 0023-852X</identifier><identifier>EISSN: 1531-4995</identifier><identifier>DOI: 10.1097/mlg.0b013e31806146e5</identifier><identifier>PMID: 17592396</identifier><identifier>CODEN: LARYA8</identifier><language>eng</language><publisher>Hoboken, NJ: John Wiley &amp; Sons, Inc</publisher><subject>Adolescent ; Adult ; Aged ; Antigens, Neoplasm - metabolism ; Biological and medical sciences ; Biomarkers, Tumor - immunology ; Biomarkers, Tumor - metabolism ; Child ; Dermatology ; Female ; Follow-Up Studies ; Head and Neck Neoplasms - immunology ; Head and Neck Neoplasms - metabolism ; Head and Neck Neoplasms - pathology ; Humans ; Immunohistochemistry ; Lymph Node Excision ; Lymph Nodes - pathology ; Lymph Nodes - surgery ; Lymphatic Metastasis ; Male ; MART-1 Antigen ; Medical sciences ; melanoma ; Melanoma - immunology ; Melanoma - metabolism ; Melanoma - secondary ; Melanoma-Specific Antigens ; metastasis ; Microphthalmia-Associated Transcription Factor - metabolism ; Middle Aged ; Monophenol Monooxygenase - metabolism ; Neck ; neck dissection ; Neoplasm Proteins - metabolism ; Otorhinolaryngology. Stomatology ; outcomes ; Prognosis ; Retrospective Studies ; S100 Proteins - metabolism ; Scalp ; sentinel lymph node ; Sentinel Lymph Node Biopsy ; Skin Neoplasms - immunology ; Skin Neoplasms - metabolism ; Skin Neoplasms - pathology ; Tumors of the skin and soft tissue. 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Study Design: Retrospective. Methods: There were 22 patients, 4 females and 18 males. Sentinel lymph nodes (SLN) were localized via preoperative lymphoscintigraphy, intraoperative gamma probe, and Lymphazurin injection. SLNs were stained with hematoxylin‐eosin, S‐100, HMB‐45, Melan‐A, micropthalmia transcription factor, and tyrosinase. SLNs were grouped into cervical (levels 1–5) and extracervical (parotid, suboccipital, retroauricular) regions. Results: There were 13 posterior and 9 anterior SMs. The first SNB were mapped to the extracervical regions in 77% of posterior and 78% of anterior lesions. SLN number ranged from 1 to 5. Ten patients had positive SLNs (PSLN). Forty percent of the PSLN group had SLNs mapped in both cervical and extracervical sites. Six underwent completion lymphadenectomy, with no additional positive nodes identified. No significant difference between PSLN and negative sentinel node (NSLN) patients was seen when compared by SLN number, Breslow's thickness, tumor ulceration, and clinical outcomes. Mean follow‐up was 35 months. One patient died of disease. One isolated regional recurrence occurred. Sixty percent of PSLN and 92% of NSLN patients were recurrence free at last follow‐up. One distant metastasis occurred in the NSLN group, and one local, one regional, and two patients with distant metastases were in the PSLN group at the time of last follow‐up. Additional IHC did not detect other metastases in the NSLN group. Conclusions: SM is aggressive, as demonstrated by the high rate of SLN metastases, and there were no significant histopathologic factors in the primary tumor that predicted the presence of SLN metastases. SNB was accurate. The majority of first SLNs were localized in extracervical basins.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Antigens, Neoplasm - metabolism</subject><subject>Biological and medical sciences</subject><subject>Biomarkers, Tumor - immunology</subject><subject>Biomarkers, Tumor - metabolism</subject><subject>Child</subject><subject>Dermatology</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Head and Neck Neoplasms - immunology</subject><subject>Head and Neck Neoplasms - metabolism</subject><subject>Head and Neck Neoplasms - pathology</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Lymph Node Excision</subject><subject>Lymph Nodes - pathology</subject><subject>Lymph Nodes - surgery</subject><subject>Lymphatic Metastasis</subject><subject>Male</subject><subject>MART-1 Antigen</subject><subject>Medical sciences</subject><subject>melanoma</subject><subject>Melanoma - immunology</subject><subject>Melanoma - metabolism</subject><subject>Melanoma - secondary</subject><subject>Melanoma-Specific Antigens</subject><subject>metastasis</subject><subject>Microphthalmia-Associated Transcription Factor - metabolism</subject><subject>Middle Aged</subject><subject>Monophenol Monooxygenase - metabolism</subject><subject>Neck</subject><subject>neck dissection</subject><subject>Neoplasm Proteins - metabolism</subject><subject>Otorhinolaryngology. Stomatology</subject><subject>outcomes</subject><subject>Prognosis</subject><subject>Retrospective Studies</subject><subject>S100 Proteins - metabolism</subject><subject>Scalp</subject><subject>sentinel lymph node</subject><subject>Sentinel Lymph Node Biopsy</subject><subject>Skin Neoplasms - immunology</subject><subject>Skin Neoplasms - metabolism</subject><subject>Skin Neoplasms - pathology</subject><subject>Tumors of the skin and soft tissue. Premalignant lesions</subject><issn>0023-852X</issn><issn>1531-4995</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkE1PAjEQQBujEUT_gTFc9LY4_dq2NwkqkqBG_EBPTdvtmtVdFrcQ5d-7ZokknjzN5c2byUPoEEMPgxKnRf7aAwuYeoolxJjFnm-hNuYUR0wpvo3aAIRGkpPnFtoL4Q0AC8phF7Ww4IpQFbdRd5RkZVjNXGVC5kO3TLv3zuTz7rXPzawszD7aSU0e_MF6dtDj5cXD4Coa3w5Hg_44coyCjLDiwqbUxYZISb3nTHjlklhgbq0S1HEnZEqZIiRNnHFMGQrWcsEseEss7aCTxjuvyo-lDwtdZMH5vP7Cl8ugY0kI44TVIGtAV5UhVD7V8yorTLXSGPRPGV2X0X_L1GtHa__SFj7ZLK1T1MDxGjChLpBWZuaysOGkiqWQqubOGu4zy_3qX8f1uD954ZxhLECCrBVRo8jCwn_9Kkz1rmNBBdfTm6Ge3mFxPn6aaKDfGWCN0Q</recordid><startdate>200708</startdate><enddate>200708</enddate><creator>Rigual, Nestor R.</creator><creator>Cheney, Richard T.</creator><creator>Iwenofu, Obiajulu H.</creator><creator>Li, Qiang</creator><creator>Loree, Thom R.</creator><creator>Popat, Saurin R.</creator><creator>Merzianu, Mihai</creator><general>John Wiley &amp; Sons, Inc</general><general>Wiley-Blackwell</general><scope>BSCLL</scope><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><scope>8BM</scope></search><sort><creationdate>200708</creationdate><title>Idiosyncrasies of Scalp Melanoma</title><author>Rigual, Nestor R. ; Cheney, Richard T. ; Iwenofu, Obiajulu H. ; Li, Qiang ; Loree, Thom R. ; Popat, Saurin R. ; Merzianu, Mihai</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4308-1957bf3c6a2883ee547e9cd6715bb973c5c78f34922fdcac49a30bb574b0eb2b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Antigens, Neoplasm - metabolism</topic><topic>Biological and medical sciences</topic><topic>Biomarkers, Tumor - immunology</topic><topic>Biomarkers, Tumor - metabolism</topic><topic>Child</topic><topic>Dermatology</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Head and Neck Neoplasms - immunology</topic><topic>Head and Neck Neoplasms - metabolism</topic><topic>Head and Neck Neoplasms - pathology</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Lymph Node Excision</topic><topic>Lymph Nodes - pathology</topic><topic>Lymph Nodes - surgery</topic><topic>Lymphatic Metastasis</topic><topic>Male</topic><topic>MART-1 Antigen</topic><topic>Medical sciences</topic><topic>melanoma</topic><topic>Melanoma - immunology</topic><topic>Melanoma - metabolism</topic><topic>Melanoma - secondary</topic><topic>Melanoma-Specific Antigens</topic><topic>metastasis</topic><topic>Microphthalmia-Associated Transcription Factor - metabolism</topic><topic>Middle Aged</topic><topic>Monophenol Monooxygenase - metabolism</topic><topic>Neck</topic><topic>neck dissection</topic><topic>Neoplasm Proteins - metabolism</topic><topic>Otorhinolaryngology. Stomatology</topic><topic>outcomes</topic><topic>Prognosis</topic><topic>Retrospective Studies</topic><topic>S100 Proteins - metabolism</topic><topic>Scalp</topic><topic>sentinel lymph node</topic><topic>Sentinel Lymph Node Biopsy</topic><topic>Skin Neoplasms - immunology</topic><topic>Skin Neoplasms - metabolism</topic><topic>Skin Neoplasms - pathology</topic><topic>Tumors of the skin and soft tissue. Premalignant lesions</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rigual, Nestor R.</creatorcontrib><creatorcontrib>Cheney, Richard T.</creatorcontrib><creatorcontrib>Iwenofu, Obiajulu H.</creatorcontrib><creatorcontrib>Li, Qiang</creatorcontrib><creatorcontrib>Loree, Thom R.</creatorcontrib><creatorcontrib>Popat, Saurin R.</creatorcontrib><creatorcontrib>Merzianu, Mihai</creatorcontrib><collection>Istex</collection><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><collection>ComDisDome</collection><jtitle>The Laryngoscope</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rigual, Nestor R.</au><au>Cheney, Richard T.</au><au>Iwenofu, Obiajulu H.</au><au>Li, Qiang</au><au>Loree, Thom R.</au><au>Popat, Saurin R.</au><au>Merzianu, Mihai</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Idiosyncrasies of Scalp Melanoma</atitle><jtitle>The Laryngoscope</jtitle><addtitle>The Laryngoscope</addtitle><date>2007-08</date><risdate>2007</risdate><volume>117</volume><issue>8</issue><spage>1354</spage><epage>1358</epage><pages>1354-1358</pages><issn>0023-852X</issn><eissn>1531-4995</eissn><coden>LARYA8</coden><abstract>Objectives/Hypothesis: Examine the accuracy of sentinel lymph node biopsy (SNB) in scalp melanoma (SM), patterns of nodal metastases, patient outcomes, and the utility of immunohistochemistry (IHC) in SNB evaluation. Study Design: Retrospective. Methods: There were 22 patients, 4 females and 18 males. Sentinel lymph nodes (SLN) were localized via preoperative lymphoscintigraphy, intraoperative gamma probe, and Lymphazurin injection. SLNs were stained with hematoxylin‐eosin, S‐100, HMB‐45, Melan‐A, micropthalmia transcription factor, and tyrosinase. SLNs were grouped into cervical (levels 1–5) and extracervical (parotid, suboccipital, retroauricular) regions. Results: There were 13 posterior and 9 anterior SMs. The first SNB were mapped to the extracervical regions in 77% of posterior and 78% of anterior lesions. SLN number ranged from 1 to 5. Ten patients had positive SLNs (PSLN). Forty percent of the PSLN group had SLNs mapped in both cervical and extracervical sites. Six underwent completion lymphadenectomy, with no additional positive nodes identified. No significant difference between PSLN and negative sentinel node (NSLN) patients was seen when compared by SLN number, Breslow's thickness, tumor ulceration, and clinical outcomes. Mean follow‐up was 35 months. One patient died of disease. One isolated regional recurrence occurred. Sixty percent of PSLN and 92% of NSLN patients were recurrence free at last follow‐up. One distant metastasis occurred in the NSLN group, and one local, one regional, and two patients with distant metastases were in the PSLN group at the time of last follow‐up. Additional IHC did not detect other metastases in the NSLN group. Conclusions: SM is aggressive, as demonstrated by the high rate of SLN metastases, and there were no significant histopathologic factors in the primary tumor that predicted the presence of SLN metastases. SNB was accurate. The majority of first SLNs were localized in extracervical basins.</abstract><cop>Hoboken, NJ</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>17592396</pmid><doi>10.1097/mlg.0b013e31806146e5</doi><tpages>5</tpages></addata></record>
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subjects Adolescent
Adult
Aged
Antigens, Neoplasm - metabolism
Biological and medical sciences
Biomarkers, Tumor - immunology
Biomarkers, Tumor - metabolism
Child
Dermatology
Female
Follow-Up Studies
Head and Neck Neoplasms - immunology
Head and Neck Neoplasms - metabolism
Head and Neck Neoplasms - pathology
Humans
Immunohistochemistry
Lymph Node Excision
Lymph Nodes - pathology
Lymph Nodes - surgery
Lymphatic Metastasis
Male
MART-1 Antigen
Medical sciences
melanoma
Melanoma - immunology
Melanoma - metabolism
Melanoma - secondary
Melanoma-Specific Antigens
metastasis
Microphthalmia-Associated Transcription Factor - metabolism
Middle Aged
Monophenol Monooxygenase - metabolism
Neck
neck dissection
Neoplasm Proteins - metabolism
Otorhinolaryngology. Stomatology
outcomes
Prognosis
Retrospective Studies
S100 Proteins - metabolism
Scalp
sentinel lymph node
Sentinel Lymph Node Biopsy
Skin Neoplasms - immunology
Skin Neoplasms - metabolism
Skin Neoplasms - pathology
Tumors of the skin and soft tissue. Premalignant lesions
title Idiosyncrasies of Scalp Melanoma
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