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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:American family physician 2001-04, Vol.63 (7), p.1359-1374
Hauptverfasser: Goldstein, B G, Goldstein, A O
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1374
container_issue 7
container_start_page 1359
container_title American family physician
container_volume 63
creator Goldstein, B G
Goldstein, A O
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.
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_77053086</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>77053086</sourcerecordid><originalsourceid>FETCH-LOGICAL-p234t-285e56c6c44da68ffb8c8b85fe9c6311fa0a7353aa55d00ab5b363719258e9ec3</originalsourceid><addsrcrecordid>eNpdkM1KxDAURrNQnHH0FaS4cFdJmuanSxl1FAbczIC7cpvelA5NUpt24dsbcNy4uhw4fBzuBVlTSotcc_25ItcxnhIqwaorsmKMMyoFXZPH5x46H2IfM_Bt5sBDhw79nAWbaOg7DwkcDuCDgxtyaWGIeHu-G3J8fTls3_L9x-59-7TPx4KXc15ogUIaacqyBamtbbTRjRYWKyM5YxYoKC44gBAtpdCIhkuuWFUIjRUaviEPv7vjFL4WjHPt-mhwSBUYllgrRQWnWibx_p94CsvkU1udSgopaaWSdHeWlsZhW49T72D6rv_ewH8A7LZWiQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>234266097</pqid></control><display><type>article</type><title>Diagnosis and management of malignant melanoma</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>Goldstein, B G ; Goldstein, A O</creator><creatorcontrib>Goldstein, B G ; Goldstein, A O</creatorcontrib><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><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 &amp; Allied Health Database</collection><collection>Health &amp; 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 &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Consumer Health Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Healthcare Administration Database</collection><collection>Nursing &amp; 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>
fulltext fulltext
identifier ISSN: 0002-838X
ispartof American family physician, 2001-04, Vol.63 (7), p.1359-1374
issn 0002-838X
language eng
recordid cdi_proquest_miscellaneous_77053086
source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T23%3A27%3A56IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Diagnosis%20and%20management%20of%20malignant%20melanoma&rft.jtitle=American%20family%20physician&rft.au=Goldstein,%20B%20G&rft.date=2001-04-01&rft.volume=63&rft.issue=7&rft.spage=1359&rft.epage=1374&rft.pages=1359-1374&rft.issn=0002-838X&rft.coden=AFPYBF&rft_id=info:doi/&rft_dat=%3Cproquest_pubme%3E77053086%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=234266097&rft_id=info:pmid/11310650&rfr_iscdi=true