Malignant melanoma in xeroderma pigmentosum patients: report of five cases
Xeroderma pigmentosum is a rare genetic disease transmitted via a recessive gene with an altered reaction of the epidermis to light. Fifty per cent of patients develop a skin tumour by 8 years of age. The majority of patients may have multiple tumours, but metastasis is rare. In the last 25 years we...
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Veröffentlicht in: | European journal of surgical oncology 1997-02, Vol.23 (1), p.43-47 |
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creator | Kocabalkan, Oya Özgür, Figen Erk, Yücel Gürsu, K. Güler Güngen, Yücel |
description | Xeroderma pigmentosum is a rare genetic disease transmitted via a recessive gene with an altered reaction of the epidermis to light. Fifty per cent of patients develop a skin tumour by 8 years of age. The majority of patients may have multiple tumours, but metastasis is rare. In the last 25 years we have treated 24 xeroderma pigmentosum patients in our clinic. Only five patients had developed cutaneous malignant melanoma during their follow-up. Three of the patients were from the same family, melanoma occurring in three of five affected individuals. All xeroderma pigmentosum patients with malignant melanoma had received classical treatment modalities. Except one case of fulminant pattern, all four patients had long disease-free survival. Although early detection and treatment of these cutaneous malignancies will reduce morbidity and mortality, genetic counselling remains the most important protective measure for xeroderma pigmentosum. |
doi_str_mv | 10.1016/S0748-7983(97)80141-2 |
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Although early detection and treatment of these cutaneous malignancies will reduce morbidity and mortality, genetic counselling remains the most important protective measure for xeroderma pigmentosum.</description><identifier>ISSN: 0748-7983</identifier><identifier>EISSN: 1532-2157</identifier><identifier>DOI: 10.1016/S0748-7983(97)80141-2</identifier><identifier>PMID: 9066746</identifier><identifier>CODEN: EJSOE7</identifier><language>eng</language><publisher>Amsterdam: Elsevier Ltd</publisher><subject>Adult ; Biological and medical sciences ; Cell Transformation, Neoplastic ; Child ; Dermatology ; Disease-Free Survival ; genetic disease ; Humans ; Male ; malignant melanoma ; Medical sciences ; Melanoma - etiology ; Melanoma - genetics ; Melanoma - pathology ; Pedigree ; Pigmentary diseases of the skin ; Skin Diseases - complications ; Skin Diseases - pathology ; Skin Neoplasms - etiology ; Skin Neoplasms - genetics ; Skin Neoplasms - pathology ; Tumors of the skin and soft tissue. 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Güler</creatorcontrib><creatorcontrib>Güngen, Yücel</creatorcontrib><title>Malignant melanoma in xeroderma pigmentosum patients: report of five cases</title><title>European journal of surgical oncology</title><addtitle>Eur J Surg Oncol</addtitle><description>Xeroderma pigmentosum is a rare genetic disease transmitted via a recessive gene with an altered reaction of the epidermis to light. Fifty per cent of patients develop a skin tumour by 8 years of age. The majority of patients may have multiple tumours, but metastasis is rare. In the last 25 years we have treated 24 xeroderma pigmentosum patients in our clinic. Only five patients had developed cutaneous malignant melanoma during their follow-up. Three of the patients were from the same family, melanoma occurring in three of five affected individuals. All xeroderma pigmentosum patients with malignant melanoma had received classical treatment modalities. Except one case of fulminant pattern, all four patients had long disease-free survival. Although early detection and treatment of these cutaneous malignancies will reduce morbidity and mortality, genetic counselling remains the most important protective measure for xeroderma pigmentosum.</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Cell Transformation, Neoplastic</subject><subject>Child</subject><subject>Dermatology</subject><subject>Disease-Free Survival</subject><subject>genetic disease</subject><subject>Humans</subject><subject>Male</subject><subject>malignant melanoma</subject><subject>Medical sciences</subject><subject>Melanoma - etiology</subject><subject>Melanoma - genetics</subject><subject>Melanoma - pathology</subject><subject>Pedigree</subject><subject>Pigmentary diseases of the skin</subject><subject>Skin Diseases - complications</subject><subject>Skin Diseases - pathology</subject><subject>Skin Neoplasms - etiology</subject><subject>Skin Neoplasms - genetics</subject><subject>Skin Neoplasms - pathology</subject><subject>Tumors of the skin and soft tissue. Premalignant lesions</subject><subject>xeroderma pigmentosum</subject><subject>Xeroderma Pigmentosum - complications</subject><subject>Xeroderma Pigmentosum - pathology</subject><issn>0748-7983</issn><issn>1532-2157</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1P3DAQQK2qCLa0PwEph6qih4Adxx67F4QQ0FagHtqeLa89RkZJnNpZVP59Dbvaa08zo3nzoUfICaNnjDJ5_pNCr1rQip9q-Kwo61nbvSErJnjXdkzAW7LaI0fkXSmPlFLNQR-SQ02lhF6uyPd7O8SHyU5LM-JgpzTaJk7NX8zJY67FHB9GnJZUNmMz2yXWvHxpMs4pL00KTYhP2DhbsLwnB8EOBT_s4jH5fXP96-pre_fj9tvV5V3ruNJLyz3A2oXgpfYenOwBFAZQspc97ZUEqiWGtRIgkHvGar62rhO64wKD6_kx-bTdO-f0Z4NlMWMsDof6PaZNMaAUMKVEBcUWdDmVkjGYOcfR5mfDqHlxaF4dmhdBRoN5dWi6OneyO7BZj-j3Uztptf9x17fF2SFkO7lY9lgnqRScVexii2GV8RQxm-KqPoc-ZnSL8Sn-55F_SRmOcA</recordid><startdate>19970201</startdate><enddate>19970201</enddate><creator>Kocabalkan, Oya</creator><creator>Özgür, Figen</creator><creator>Erk, Yücel</creator><creator>Gürsu, K. 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Güler ; Güngen, Yücel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c389t-3d77bcffd69dd7c64778ef78646404867096efb8575e3d11efbbac259235efc43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Cell Transformation, Neoplastic</topic><topic>Child</topic><topic>Dermatology</topic><topic>Disease-Free Survival</topic><topic>genetic disease</topic><topic>Humans</topic><topic>Male</topic><topic>malignant melanoma</topic><topic>Medical sciences</topic><topic>Melanoma - etiology</topic><topic>Melanoma - genetics</topic><topic>Melanoma - pathology</topic><topic>Pedigree</topic><topic>Pigmentary diseases of the skin</topic><topic>Skin Diseases - complications</topic><topic>Skin Diseases - pathology</topic><topic>Skin Neoplasms - etiology</topic><topic>Skin Neoplasms - genetics</topic><topic>Skin Neoplasms - pathology</topic><topic>Tumors of the skin and soft tissue. Premalignant lesions</topic><topic>xeroderma pigmentosum</topic><topic>Xeroderma Pigmentosum - complications</topic><topic>Xeroderma Pigmentosum - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kocabalkan, Oya</creatorcontrib><creatorcontrib>Özgür, Figen</creatorcontrib><creatorcontrib>Erk, Yücel</creatorcontrib><creatorcontrib>Gürsu, K. 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Güler</au><au>Güngen, Yücel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Malignant melanoma in xeroderma pigmentosum patients: report of five cases</atitle><jtitle>European journal of surgical oncology</jtitle><addtitle>Eur J Surg Oncol</addtitle><date>1997-02-01</date><risdate>1997</risdate><volume>23</volume><issue>1</issue><spage>43</spage><epage>47</epage><pages>43-47</pages><issn>0748-7983</issn><eissn>1532-2157</eissn><coden>EJSOE7</coden><abstract>Xeroderma pigmentosum is a rare genetic disease transmitted via a recessive gene with an altered reaction of the epidermis to light. Fifty per cent of patients develop a skin tumour by 8 years of age. The majority of patients may have multiple tumours, but metastasis is rare. In the last 25 years we have treated 24 xeroderma pigmentosum patients in our clinic. Only five patients had developed cutaneous malignant melanoma during their follow-up. Three of the patients were from the same family, melanoma occurring in three of five affected individuals. All xeroderma pigmentosum patients with malignant melanoma had received classical treatment modalities. Except one case of fulminant pattern, all four patients had long disease-free survival. Although early detection and treatment of these cutaneous malignancies will reduce morbidity and mortality, genetic counselling remains the most important protective measure for xeroderma pigmentosum.</abstract><cop>Amsterdam</cop><pub>Elsevier Ltd</pub><pmid>9066746</pmid><doi>10.1016/S0748-7983(97)80141-2</doi><tpages>5</tpages></addata></record> |
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subjects | Adult Biological and medical sciences Cell Transformation, Neoplastic Child Dermatology Disease-Free Survival genetic disease Humans Male malignant melanoma Medical sciences Melanoma - etiology Melanoma - genetics Melanoma - pathology Pedigree Pigmentary diseases of the skin Skin Diseases - complications Skin Diseases - pathology Skin Neoplasms - etiology Skin Neoplasms - genetics Skin Neoplasms - pathology Tumors of the skin and soft tissue. Premalignant lesions xeroderma pigmentosum Xeroderma Pigmentosum - complications Xeroderma Pigmentosum - pathology |
title | Malignant melanoma in xeroderma pigmentosum patients: report of five cases |
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