Gefitinib-Induced Paronychia: Response to Autologous Platelet-Rich Plasma
BACKGROUND Paronychia has been reported in as many as 10% of patients treated with gefitinib. Although conservative management and treatment with topical or systemic antibiotics are beneficial, no effective method exists for intractable cases. Platelet-rich plasma (PRP) consists of a high concentrat...
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Veröffentlicht in: | Archives of dermatology (1960) 2012-12, Vol.148 (12), p.1399-1402 |
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container_title | Archives of dermatology (1960) |
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creator | Kwon, Soon-Hyo Choi, Jae-Woo Hong, Jong-Soo Byun, Sang-Young Park, Kyoung-Chan Youn, Sang-Woong Huh, Chang-Hun Na, Jung-Im |
description | BACKGROUND Paronychia has been reported in as many as 10% of patients treated with gefitinib. Although conservative management and treatment with topical or systemic antibiotics are beneficial, no effective method exists for intractable cases. Platelet-rich plasma (PRP) consists of a high concentration of platelets that promote wound healing through chemotaxis, cell proliferation, angiogenesis, and tissue remodeling. OBSERVATIONS We herein report a refractory case of gefitinib-induced paronychia successfully treated with autologous PRP. A 68-year-old woman who had been diagnosed as having lung adenocarcinoma with multiple bone and brain metastases initiated gefitinib therapy at an oral dose of 250 mg/d. After 1 month, multiple paronychia with periungual granulation appeared on the nail fold of the first, second, and third toenails of both feet. Because the paronychia recurred repeatedly despite use of a topical antibiotic, topical corticosteroid, and short-term systemic antibiotic, she started PRP treatment. After 3 months, the lesion showed marked improvement with minimal pain or discharge. CONCLUSION This case highlights the therapeutic challenges of using PRP to promote tissue repair in intractable gefitinib-induced paronychia and merits further investigation. |
doi_str_mv | 10.1001/archdermatol.2012.3022 |
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Although conservative management and treatment with topical or systemic antibiotics are beneficial, no effective method exists for intractable cases. Platelet-rich plasma (PRP) consists of a high concentration of platelets that promote wound healing through chemotaxis, cell proliferation, angiogenesis, and tissue remodeling. OBSERVATIONS We herein report a refractory case of gefitinib-induced paronychia successfully treated with autologous PRP. A 68-year-old woman who had been diagnosed as having lung adenocarcinoma with multiple bone and brain metastases initiated gefitinib therapy at an oral dose of 250 mg/d. After 1 month, multiple paronychia with periungual granulation appeared on the nail fold of the first, second, and third toenails of both feet. Because the paronychia recurred repeatedly despite use of a topical antibiotic, topical corticosteroid, and short-term systemic antibiotic, she started PRP treatment. After 3 months, the lesion showed marked improvement with minimal pain or discharge. CONCLUSION This case highlights the therapeutic challenges of using PRP to promote tissue repair in intractable gefitinib-induced paronychia and merits further investigation.</description><identifier>ISSN: 0003-987X</identifier><identifier>ISSN: 2168-6068</identifier><identifier>EISSN: 1538-3652</identifier><identifier>EISSN: 2168-6084</identifier><identifier>DOI: 10.1001/archdermatol.2012.3022</identifier><identifier>PMID: 22986691</identifier><identifier>CODEN: ARDEAC</identifier><language>eng</language><publisher>Chicago, IL: American Medical Association</publisher><subject>Aged ; Angiogenesis ; Antibiotics ; Antineoplastic Agents - adverse effects ; Biological and medical sciences ; Dermatology ; Drug therapy ; Female ; Humans ; Lung Neoplasms - drug therapy ; Medical sciences ; Paronychia - chemically induced ; Paronychia - therapy ; Plasma ; Platelet-Rich Plasma ; Quinazolines - adverse effects ; Skin cancer</subject><ispartof>Archives of dermatology (1960), 2012-12, Vol.148 (12), p.1399-1402</ispartof><rights>2014 INIST-CNRS</rights><rights>Copyright American Medical Association Dec 2012</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://jamanetwork.com/journals/jamadermatology/articlepdf/10.1001/archdermatol.2012.3022$$EPDF$$P50$$Gama$$H</linktopdf><linktohtml>$$Uhttps://jamanetwork.com/journals/jamadermatology/fullarticle/10.1001/archdermatol.2012.3022$$EHTML$$P50$$Gama$$H</linktohtml><link.rule.ids>64,314,780,784,3340,27924,27925,76489,76492</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26720549$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22986691$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kwon, Soon-Hyo</creatorcontrib><creatorcontrib>Choi, Jae-Woo</creatorcontrib><creatorcontrib>Hong, Jong-Soo</creatorcontrib><creatorcontrib>Byun, Sang-Young</creatorcontrib><creatorcontrib>Park, Kyoung-Chan</creatorcontrib><creatorcontrib>Youn, Sang-Woong</creatorcontrib><creatorcontrib>Huh, Chang-Hun</creatorcontrib><creatorcontrib>Na, Jung-Im</creatorcontrib><title>Gefitinib-Induced Paronychia: Response to Autologous Platelet-Rich Plasma</title><title>Archives of dermatology (1960)</title><addtitle>Arch Dermatol</addtitle><description>BACKGROUND Paronychia has been reported in as many as 10% of patients treated with gefitinib. Although conservative management and treatment with topical or systemic antibiotics are beneficial, no effective method exists for intractable cases. Platelet-rich plasma (PRP) consists of a high concentration of platelets that promote wound healing through chemotaxis, cell proliferation, angiogenesis, and tissue remodeling. OBSERVATIONS We herein report a refractory case of gefitinib-induced paronychia successfully treated with autologous PRP. A 68-year-old woman who had been diagnosed as having lung adenocarcinoma with multiple bone and brain metastases initiated gefitinib therapy at an oral dose of 250 mg/d. After 1 month, multiple paronychia with periungual granulation appeared on the nail fold of the first, second, and third toenails of both feet. Because the paronychia recurred repeatedly despite use of a topical antibiotic, topical corticosteroid, and short-term systemic antibiotic, she started PRP treatment. After 3 months, the lesion showed marked improvement with minimal pain or discharge. CONCLUSION This case highlights the therapeutic challenges of using PRP to promote tissue repair in intractable gefitinib-induced paronychia and merits further investigation.</description><subject>Aged</subject><subject>Angiogenesis</subject><subject>Antibiotics</subject><subject>Antineoplastic Agents - adverse effects</subject><subject>Biological and medical sciences</subject><subject>Dermatology</subject><subject>Drug therapy</subject><subject>Female</subject><subject>Humans</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Medical sciences</subject><subject>Paronychia - chemically induced</subject><subject>Paronychia - therapy</subject><subject>Plasma</subject><subject>Platelet-Rich Plasma</subject><subject>Quinazolines - adverse effects</subject><subject>Skin cancer</subject><issn>0003-987X</issn><issn>2168-6068</issn><issn>1538-3652</issn><issn>2168-6084</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkE1LHEEQhhtJ0I3mD3iQgSDkMmt19fSXN5HELAgRUcit6enpcUdmptfumYP_Pr3sJoqnoornrSoeQs4oLCkAvbDRrRsfBzuFfolAcckA8YAsKGeqZILjJ7IAAFZqJf8ckS8pPeccKoWH5AhRKyE0XZDVjW-7qRu7ulyNzex8U9zZGMZXt-7sZXHv0yaMyRdTKK7mfCs8hTkVd72dfO-n8r5z622XBntCPre2T_7rvh6Tx58_Hq5_lbe_b1bXV7elZYxPZeWU0EyDr1HZloKniioBTHPP0FeY51oCqzmvW5DgOCqQvEHbtlRKV7Nj8n23dxPDy-zTZIYuOd_3dvT5N0MloOCykjSj3z6gz2GOY_7OUKyQ0wpElSmxo1wMKUXfmk3sBhtfDQWzlW3eyzZb2WYrOwfP9uvnevDN_9g_uxk43wM2Odu30Y6uS2-ckAi80pk73XF2sG_HGVdcc_YXqlmR3w</recordid><startdate>20121201</startdate><enddate>20121201</enddate><creator>Kwon, Soon-Hyo</creator><creator>Choi, Jae-Woo</creator><creator>Hong, Jong-Soo</creator><creator>Byun, Sang-Young</creator><creator>Park, Kyoung-Chan</creator><creator>Youn, Sang-Woong</creator><creator>Huh, Chang-Hun</creator><creator>Na, Jung-Im</creator><general>American Medical Association</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>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>20121201</creationdate><title>Gefitinib-Induced Paronychia: Response to Autologous Platelet-Rich Plasma</title><author>Kwon, Soon-Hyo ; Choi, Jae-Woo ; Hong, Jong-Soo ; Byun, Sang-Young ; Park, Kyoung-Chan ; Youn, Sang-Woong ; Huh, Chang-Hun ; Na, Jung-Im</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a335t-4c869390eb28af10e181860395e32e42eb29703b55bf070c528075d2aff177cb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Aged</topic><topic>Angiogenesis</topic><topic>Antibiotics</topic><topic>Antineoplastic Agents - adverse effects</topic><topic>Biological and medical sciences</topic><topic>Dermatology</topic><topic>Drug therapy</topic><topic>Female</topic><topic>Humans</topic><topic>Lung Neoplasms - drug therapy</topic><topic>Medical sciences</topic><topic>Paronychia - chemically induced</topic><topic>Paronychia - therapy</topic><topic>Plasma</topic><topic>Platelet-Rich Plasma</topic><topic>Quinazolines - adverse effects</topic><topic>Skin cancer</topic><toplevel>online_resources</toplevel><creatorcontrib>Kwon, Soon-Hyo</creatorcontrib><creatorcontrib>Choi, Jae-Woo</creatorcontrib><creatorcontrib>Hong, Jong-Soo</creatorcontrib><creatorcontrib>Byun, Sang-Young</creatorcontrib><creatorcontrib>Park, Kyoung-Chan</creatorcontrib><creatorcontrib>Youn, Sang-Woong</creatorcontrib><creatorcontrib>Huh, Chang-Hun</creatorcontrib><creatorcontrib>Na, Jung-Im</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>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Archives of dermatology (1960)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kwon, Soon-Hyo</au><au>Choi, Jae-Woo</au><au>Hong, Jong-Soo</au><au>Byun, Sang-Young</au><au>Park, Kyoung-Chan</au><au>Youn, Sang-Woong</au><au>Huh, Chang-Hun</au><au>Na, Jung-Im</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gefitinib-Induced Paronychia: Response to Autologous Platelet-Rich Plasma</atitle><jtitle>Archives of dermatology (1960)</jtitle><addtitle>Arch Dermatol</addtitle><date>2012-12-01</date><risdate>2012</risdate><volume>148</volume><issue>12</issue><spage>1399</spage><epage>1402</epage><pages>1399-1402</pages><issn>0003-987X</issn><issn>2168-6068</issn><eissn>1538-3652</eissn><eissn>2168-6084</eissn><coden>ARDEAC</coden><abstract>BACKGROUND Paronychia has been reported in as many as 10% of patients treated with gefitinib. Although conservative management and treatment with topical or systemic antibiotics are beneficial, no effective method exists for intractable cases. Platelet-rich plasma (PRP) consists of a high concentration of platelets that promote wound healing through chemotaxis, cell proliferation, angiogenesis, and tissue remodeling. OBSERVATIONS We herein report a refractory case of gefitinib-induced paronychia successfully treated with autologous PRP. A 68-year-old woman who had been diagnosed as having lung adenocarcinoma with multiple bone and brain metastases initiated gefitinib therapy at an oral dose of 250 mg/d. After 1 month, multiple paronychia with periungual granulation appeared on the nail fold of the first, second, and third toenails of both feet. Because the paronychia recurred repeatedly despite use of a topical antibiotic, topical corticosteroid, and short-term systemic antibiotic, she started PRP treatment. After 3 months, the lesion showed marked improvement with minimal pain or discharge. CONCLUSION This case highlights the therapeutic challenges of using PRP to promote tissue repair in intractable gefitinib-induced paronychia and merits further investigation.</abstract><cop>Chicago, IL</cop><pub>American Medical Association</pub><pmid>22986691</pmid><doi>10.1001/archdermatol.2012.3022</doi><tpages>4</tpages></addata></record> |
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subjects | Aged Angiogenesis Antibiotics Antineoplastic Agents - adverse effects Biological and medical sciences Dermatology Drug therapy Female Humans Lung Neoplasms - drug therapy Medical sciences Paronychia - chemically induced Paronychia - therapy Plasma Platelet-Rich Plasma Quinazolines - adverse effects Skin cancer |
title | Gefitinib-Induced Paronychia: Response to Autologous Platelet-Rich Plasma |
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