Diagnosis and management of malignant melanoma
The incidence of malignant melanoma has increased in recent years more than that of any other cancer in the United States. About one in 70 people will develop melanoma during their lifetime. Family physicians should be aware that a patient with a changing mole, an atypical mole or multiple nevi is a...
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Veröffentlicht in: | American family physician 2001-04, Vol.63 (7), p.1359-1374 |
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description | The incidence of malignant melanoma has increased in recent years more than that of any other cancer in the United States. About one in 70 people will develop melanoma during their lifetime. Family physicians should be aware that a patient with a changing mole, an atypical mole or multiple nevi is at considerable risk for developing melanoma. Any mole that is suggestive of melanoma requires an excisional biopsy, primarily because prognosis and treatment are based on tumor thickness. Staging is based on tumor thickness (Breslow's measurement) and histologic level of invasion (Clark level). The current recommendations for excisional removal of confirmed melanomas include 1-cm margins for lesions measuring 1.0 mm or less in thickness and 2-cm margins for lesions from 1.0 mm to 4.0 mm in thickness or Clark's level IV of any thickness. No evidence currently shows that wider margins improve survival in patients with lesions more than 4.0 mm thick. Clinically positive nodes are typically managed by completely removing lymph nodes in the area. Elective lymph node dissection is recommended only for patients who are younger than 60 years with lesions between 1.5 mm and 4.0 mm in thickness. In the Eastern Cooperative Oncology Group Trial, interferon alfa-2b was shown to improve disease-free and overall survival, but in many other trials it has not been shown to be effective at prolonging overall survival. Vaccine therapy is currently being used to stimulate the immune system of melanoma patients with metastatic disease. |
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About one in 70 people will develop melanoma during their lifetime. Family physicians should be aware that a patient with a changing mole, an atypical mole or multiple nevi is at considerable risk for developing melanoma. Any mole that is suggestive of melanoma requires an excisional biopsy, primarily because prognosis and treatment are based on tumor thickness. Staging is based on tumor thickness (Breslow's measurement) and histologic level of invasion (Clark level). The current recommendations for excisional removal of confirmed melanomas include 1-cm margins for lesions measuring 1.0 mm or less in thickness and 2-cm margins for lesions from 1.0 mm to 4.0 mm in thickness or Clark's level IV of any thickness. No evidence currently shows that wider margins improve survival in patients with lesions more than 4.0 mm thick. Clinically positive nodes are typically managed by completely removing lymph nodes in the area. Elective lymph node dissection is recommended only for patients who are younger than 60 years with lesions between 1.5 mm and 4.0 mm in thickness. In the Eastern Cooperative Oncology Group Trial, interferon alfa-2b was shown to improve disease-free and overall survival, but in many other trials it has not been shown to be effective at prolonging overall survival. Vaccine therapy is currently being used to stimulate the immune system of melanoma patients with metastatic disease.</description><identifier>ISSN: 0002-838X</identifier><identifier>PMID: 11310650</identifier><identifier>CODEN: AFPYBF</identifier><language>eng</language><publisher>United States: American Academy of Family Physicians</publisher><subject>Antineoplastic Agents - therapeutic use ; Biopsy ; Cancer Vaccines ; Diagnosis, Differential ; Family Practice ; Female ; Health care ; Humans ; Incidence ; Interferon-alpha - therapeutic use ; Lymph Node Excision ; Male ; Medical diagnosis ; Melanoma - diagnosis ; Melanoma - epidemiology ; Melanoma - pathology ; Melanoma - therapy ; Neoplasm Staging ; Pregnancy ; Prevalence ; Recombinant Proteins ; Risk Factors ; Skin cancer ; Skin Neoplasms - diagnosis ; Skin Neoplasms - epidemiology ; Skin Neoplasms - pathology ; Skin Neoplasms - therapy ; United States - epidemiology</subject><ispartof>American family physician, 2001-04, Vol.63 (7), p.1359-1374</ispartof><rights>Copyright American Academy of Family Physicians Apr 1, 2001</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11310650$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Goldstein, B G</creatorcontrib><creatorcontrib>Goldstein, A O</creatorcontrib><title>Diagnosis and management of malignant melanoma</title><title>American family physician</title><addtitle>Am Fam Physician</addtitle><description>The incidence of malignant melanoma has increased in recent years more than that of any other cancer in the United States. About one in 70 people will develop melanoma during their lifetime. Family physicians should be aware that a patient with a changing mole, an atypical mole or multiple nevi is at considerable risk for developing melanoma. Any mole that is suggestive of melanoma requires an excisional biopsy, primarily because prognosis and treatment are based on tumor thickness. Staging is based on tumor thickness (Breslow's measurement) and histologic level of invasion (Clark level). The current recommendations for excisional removal of confirmed melanomas include 1-cm margins for lesions measuring 1.0 mm or less in thickness and 2-cm margins for lesions from 1.0 mm to 4.0 mm in thickness or Clark's level IV of any thickness. No evidence currently shows that wider margins improve survival in patients with lesions more than 4.0 mm thick. Clinically positive nodes are typically managed by completely removing lymph nodes in the area. Elective lymph node dissection is recommended only for patients who are younger than 60 years with lesions between 1.5 mm and 4.0 mm in thickness. In the Eastern Cooperative Oncology Group Trial, interferon alfa-2b was shown to improve disease-free and overall survival, but in many other trials it has not been shown to be effective at prolonging overall survival. Vaccine therapy is currently being used to stimulate the immune system of melanoma patients with metastatic disease.</description><subject>Antineoplastic Agents - therapeutic use</subject><subject>Biopsy</subject><subject>Cancer Vaccines</subject><subject>Diagnosis, Differential</subject><subject>Family Practice</subject><subject>Female</subject><subject>Health care</subject><subject>Humans</subject><subject>Incidence</subject><subject>Interferon-alpha - therapeutic use</subject><subject>Lymph Node Excision</subject><subject>Male</subject><subject>Medical diagnosis</subject><subject>Melanoma - diagnosis</subject><subject>Melanoma - epidemiology</subject><subject>Melanoma - pathology</subject><subject>Melanoma - therapy</subject><subject>Neoplasm Staging</subject><subject>Pregnancy</subject><subject>Prevalence</subject><subject>Recombinant Proteins</subject><subject>Risk Factors</subject><subject>Skin cancer</subject><subject>Skin Neoplasms - diagnosis</subject><subject>Skin Neoplasms - epidemiology</subject><subject>Skin Neoplasms - pathology</subject><subject>Skin Neoplasms - therapy</subject><subject>United States - epidemiology</subject><issn>0002-838X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNpdkM1KxDAURrNQnHH0FaS4cFdJmuanSxl1FAbczIC7cpvelA5NUpt24dsbcNy4uhw4fBzuBVlTSotcc_25ItcxnhIqwaorsmKMMyoFXZPH5x46H2IfM_Bt5sBDhw79nAWbaOg7DwkcDuCDgxtyaWGIeHu-G3J8fTls3_L9x-59-7TPx4KXc15ogUIaacqyBamtbbTRjRYWKyM5YxYoKC44gBAtpdCIhkuuWFUIjRUaviEPv7vjFL4WjHPt-mhwSBUYllgrRQWnWibx_p94CsvkU1udSgopaaWSdHeWlsZhW49T72D6rv_ewH8A7LZWiQ</recordid><startdate>20010401</startdate><enddate>20010401</enddate><creator>Goldstein, B G</creator><creator>Goldstein, A O</creator><general>American Academy of Family Physicians</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88C</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M0T</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20010401</creationdate><title>Diagnosis and management of malignant melanoma</title><author>Goldstein, B G ; Goldstein, A O</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p234t-285e56c6c44da68ffb8c8b85fe9c6311fa0a7353aa55d00ab5b363719258e9ec3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Antineoplastic Agents - therapeutic use</topic><topic>Biopsy</topic><topic>Cancer Vaccines</topic><topic>Diagnosis, Differential</topic><topic>Family Practice</topic><topic>Female</topic><topic>Health care</topic><topic>Humans</topic><topic>Incidence</topic><topic>Interferon-alpha - therapeutic use</topic><topic>Lymph Node Excision</topic><topic>Male</topic><topic>Medical diagnosis</topic><topic>Melanoma - diagnosis</topic><topic>Melanoma - epidemiology</topic><topic>Melanoma - pathology</topic><topic>Melanoma - therapy</topic><topic>Neoplasm Staging</topic><topic>Pregnancy</topic><topic>Prevalence</topic><topic>Recombinant Proteins</topic><topic>Risk Factors</topic><topic>Skin cancer</topic><topic>Skin Neoplasms - diagnosis</topic><topic>Skin Neoplasms - epidemiology</topic><topic>Skin Neoplasms - pathology</topic><topic>Skin Neoplasms - therapy</topic><topic>United States - epidemiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Goldstein, B G</creatorcontrib><creatorcontrib>Goldstein, A O</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Healthcare Administration Database (Alumni)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Healthcare Administration Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>American family physician</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Goldstein, B G</au><au>Goldstein, A O</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diagnosis and management of malignant melanoma</atitle><jtitle>American family physician</jtitle><addtitle>Am Fam Physician</addtitle><date>2001-04-01</date><risdate>2001</risdate><volume>63</volume><issue>7</issue><spage>1359</spage><epage>1374</epage><pages>1359-1374</pages><issn>0002-838X</issn><coden>AFPYBF</coden><abstract>The incidence of malignant melanoma has increased in recent years more than that of any other cancer in the United States. About one in 70 people will develop melanoma during their lifetime. Family physicians should be aware that a patient with a changing mole, an atypical mole or multiple nevi is at considerable risk for developing melanoma. Any mole that is suggestive of melanoma requires an excisional biopsy, primarily because prognosis and treatment are based on tumor thickness. Staging is based on tumor thickness (Breslow's measurement) and histologic level of invasion (Clark level). The current recommendations for excisional removal of confirmed melanomas include 1-cm margins for lesions measuring 1.0 mm or less in thickness and 2-cm margins for lesions from 1.0 mm to 4.0 mm in thickness or Clark's level IV of any thickness. No evidence currently shows that wider margins improve survival in patients with lesions more than 4.0 mm thick. Clinically positive nodes are typically managed by completely removing lymph nodes in the area. Elective lymph node dissection is recommended only for patients who are younger than 60 years with lesions between 1.5 mm and 4.0 mm in thickness. In the Eastern Cooperative Oncology Group Trial, interferon alfa-2b was shown to improve disease-free and overall survival, but in many other trials it has not been shown to be effective at prolonging overall survival. Vaccine therapy is currently being used to stimulate the immune system of melanoma patients with metastatic disease.</abstract><cop>United States</cop><pub>American Academy of Family Physicians</pub><pmid>11310650</pmid><tpages>16</tpages></addata></record> |
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subjects | Antineoplastic Agents - therapeutic use Biopsy Cancer Vaccines Diagnosis, Differential Family Practice Female Health care Humans Incidence Interferon-alpha - therapeutic use Lymph Node Excision Male Medical diagnosis Melanoma - diagnosis Melanoma - epidemiology Melanoma - pathology Melanoma - therapy Neoplasm Staging Pregnancy Prevalence Recombinant Proteins Risk Factors Skin cancer Skin Neoplasms - diagnosis Skin Neoplasms - epidemiology Skin Neoplasms - pathology Skin Neoplasms - therapy United States - epidemiology |
title | Diagnosis and management of malignant melanoma |
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