BRAF Inhibitor-Induced Antitumoral Granulomatous Dermatitis Eruption in Advanced Melanoma
Recent advances in targeting BRAF mutations, which occur in roughly 50% of the melanomas, have improved response rates and overall survival in patients with advanced disease. With the increasingly extensive use of the drug, new, nonpreventable, cutaneous and noncutaneous toxicities keep arising as i...
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Veröffentlicht in: | The American journal of dermatopathology 2015-10, Vol.37 (10), p.795-798 |
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creator | Garrido, Maria C Gutierrez, Carlota Riveiro-Falkenbach, Erica Ortiz, Pablo Rodriguez-Peralto, Jose L |
description | Recent advances in targeting BRAF mutations, which occur in roughly 50% of the melanomas, have improved response rates and overall survival in patients with advanced disease. With the increasingly extensive use of the drug, new, nonpreventable, cutaneous and noncutaneous toxicities keep arising as infrequent adverse effects. We report a 55-year-old man with a history of metastatic melanoma treated with the dabrafenib who presented, 10 months after the initiation of the treatment, with erythematous, slightly squamous, round plaques on his upper trunk and on his left upper arm. Two skin biopsies from the lesions revealed a granulomatous dermatitis in the superficial reticular dermis. One of them showed admixed abundant melanophages from tumoral melanosis. No melanoma cells were seen in any of the specimens. No interruption of the treatment was necessary. Our observation indicates that such a response may represent a positive immune activation triggered by BRAF inhibitors. The erythematous rash was initially concerning for progression of metastatic disease, which suggests that a close monitoring of the patients with advanced melanomas treated with vemurafenib is advisable to prevent unnecessary discontinuation of the therapy. |
doi_str_mv | 10.1097/DAD.0000000000000281 |
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With the increasingly extensive use of the drug, new, nonpreventable, cutaneous and noncutaneous toxicities keep arising as infrequent adverse effects. We report a 55-year-old man with a history of metastatic melanoma treated with the dabrafenib who presented, 10 months after the initiation of the treatment, with erythematous, slightly squamous, round plaques on his upper trunk and on his left upper arm. Two skin biopsies from the lesions revealed a granulomatous dermatitis in the superficial reticular dermis. One of them showed admixed abundant melanophages from tumoral melanosis. No melanoma cells were seen in any of the specimens. No interruption of the treatment was necessary. Our observation indicates that such a response may represent a positive immune activation triggered by BRAF inhibitors. 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With the increasingly extensive use of the drug, new, nonpreventable, cutaneous and noncutaneous toxicities keep arising as infrequent adverse effects. We report a 55-year-old man with a history of metastatic melanoma treated with the dabrafenib who presented, 10 months after the initiation of the treatment, with erythematous, slightly squamous, round plaques on his upper trunk and on his left upper arm. Two skin biopsies from the lesions revealed a granulomatous dermatitis in the superficial reticular dermis. One of them showed admixed abundant melanophages from tumoral melanosis. No melanoma cells were seen in any of the specimens. No interruption of the treatment was necessary. Our observation indicates that such a response may represent a positive immune activation triggered by BRAF inhibitors. The erythematous rash was initially concerning for progression of metastatic disease, which suggests that a close monitoring of the patients with advanced melanomas treated with vemurafenib is advisable to prevent unnecessary discontinuation of the therapy.</description><subject>Antineoplastic Agents - adverse effects</subject><subject>Biopsy</subject><subject>Diagnosis, Differential</subject><subject>Drug Eruptions - etiology</subject><subject>Drug Eruptions - pathology</subject><subject>Erythema - chemically induced</subject><subject>Erythema - pathology</subject><subject>Granuloma - chemically induced</subject><subject>Granuloma - pathology</subject><subject>Humans</subject><subject>Imidazoles - adverse effects</subject><subject>Male</subject><subject>Melanoma - drug therapy</subject><subject>Melanoma - enzymology</subject><subject>Melanoma - genetics</subject><subject>Melanoma - secondary</subject><subject>Middle Aged</subject><subject>Oximes - adverse effects</subject><subject>Predictive Value of Tests</subject><subject>Protein Kinase Inhibitors - adverse effects</subject><subject>Proto-Oncogene Proteins B-raf - antagonists & inhibitors</subject><subject>Proto-Oncogene Proteins B-raf - genetics</subject><subject>Proto-Oncogene Proteins B-raf - metabolism</subject><subject>Skin - drug effects</subject><subject>Skin - pathology</subject><subject>Skin Neoplasms - drug therapy</subject><subject>Skin Neoplasms - enzymology</subject><subject>Skin Neoplasms - genetics</subject><subject>Skin Neoplasms - pathology</subject><issn>0193-1091</issn><issn>1533-0311</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkNtKxDAQhoMo7rr6BiJ5ga6Tpof0su7JhRVB9MKrklMx0qZLkgq-vVlWRZybfy7-b2A-hK4JzAlU5e2yXs7h76SMnKApySlNgBJyiqZAKprEMpmgC-_fAUjKID9Hk7SgjERgil7vnuo13to3I0wYXLK1apRa4doGE8Z-cLzDG8ft2A09D8Po8VK7uJlgPF65cR_MYLGxuFYf3B7IB91xG8uX6KzlnddX3zlDL-vV8-I-2T1utot6l0ha0pAUGkByyTJR5oIJKghlmW55LolKVZvrIs-YkG2ZtYJD_EVXUpaKgoSSF1TTGcqOd6UbvHe6bfbO9Nx9NgSag6kmmmr-m4rYzRHbj6LX6hf6UUO_AF6DZQI</recordid><startdate>201510</startdate><enddate>201510</enddate><creator>Garrido, Maria C</creator><creator>Gutierrez, Carlota</creator><creator>Riveiro-Falkenbach, Erica</creator><creator>Ortiz, Pablo</creator><creator>Rodriguez-Peralto, Jose L</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>201510</creationdate><title>BRAF Inhibitor-Induced Antitumoral Granulomatous Dermatitis Eruption in Advanced Melanoma</title><author>Garrido, Maria C ; Gutierrez, Carlota ; Riveiro-Falkenbach, Erica ; Ortiz, Pablo ; Rodriguez-Peralto, Jose L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c373t-6e00cac84b75b8b3b1384efa5c1d2df5e6548bcf74fba0091e9cc7d30c07a63e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Antineoplastic Agents - adverse effects</topic><topic>Biopsy</topic><topic>Diagnosis, Differential</topic><topic>Drug Eruptions - etiology</topic><topic>Drug Eruptions - pathology</topic><topic>Erythema - chemically induced</topic><topic>Erythema - pathology</topic><topic>Granuloma - chemically induced</topic><topic>Granuloma - pathology</topic><topic>Humans</topic><topic>Imidazoles - adverse effects</topic><topic>Male</topic><topic>Melanoma - drug therapy</topic><topic>Melanoma - enzymology</topic><topic>Melanoma - genetics</topic><topic>Melanoma - secondary</topic><topic>Middle Aged</topic><topic>Oximes - adverse effects</topic><topic>Predictive Value of Tests</topic><topic>Protein Kinase Inhibitors - adverse effects</topic><topic>Proto-Oncogene Proteins B-raf - antagonists & inhibitors</topic><topic>Proto-Oncogene Proteins B-raf - genetics</topic><topic>Proto-Oncogene Proteins B-raf - metabolism</topic><topic>Skin - drug effects</topic><topic>Skin - pathology</topic><topic>Skin Neoplasms - drug therapy</topic><topic>Skin Neoplasms - enzymology</topic><topic>Skin Neoplasms - genetics</topic><topic>Skin Neoplasms - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Garrido, Maria C</creatorcontrib><creatorcontrib>Gutierrez, Carlota</creatorcontrib><creatorcontrib>Riveiro-Falkenbach, Erica</creatorcontrib><creatorcontrib>Ortiz, Pablo</creatorcontrib><creatorcontrib>Rodriguez-Peralto, Jose L</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>The American journal of dermatopathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Garrido, Maria C</au><au>Gutierrez, Carlota</au><au>Riveiro-Falkenbach, Erica</au><au>Ortiz, Pablo</au><au>Rodriguez-Peralto, Jose L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>BRAF Inhibitor-Induced Antitumoral Granulomatous Dermatitis Eruption in Advanced Melanoma</atitle><jtitle>The American journal of dermatopathology</jtitle><addtitle>Am J Dermatopathol</addtitle><date>2015-10</date><risdate>2015</risdate><volume>37</volume><issue>10</issue><spage>795</spage><epage>798</epage><pages>795-798</pages><issn>0193-1091</issn><eissn>1533-0311</eissn><abstract>Recent advances in targeting BRAF mutations, which occur in roughly 50% of the melanomas, have improved response rates and overall survival in patients with advanced disease. With the increasingly extensive use of the drug, new, nonpreventable, cutaneous and noncutaneous toxicities keep arising as infrequent adverse effects. We report a 55-year-old man with a history of metastatic melanoma treated with the dabrafenib who presented, 10 months after the initiation of the treatment, with erythematous, slightly squamous, round plaques on his upper trunk and on his left upper arm. Two skin biopsies from the lesions revealed a granulomatous dermatitis in the superficial reticular dermis. One of them showed admixed abundant melanophages from tumoral melanosis. No melanoma cells were seen in any of the specimens. No interruption of the treatment was necessary. Our observation indicates that such a response may represent a positive immune activation triggered by BRAF inhibitors. The erythematous rash was initially concerning for progression of metastatic disease, which suggests that a close monitoring of the patients with advanced melanomas treated with vemurafenib is advisable to prevent unnecessary discontinuation of the therapy.</abstract><cop>United States</cop><pmid>26381028</pmid><doi>10.1097/DAD.0000000000000281</doi><tpages>4</tpages></addata></record> |
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subjects | Antineoplastic Agents - adverse effects Biopsy Diagnosis, Differential Drug Eruptions - etiology Drug Eruptions - pathology Erythema - chemically induced Erythema - pathology Granuloma - chemically induced Granuloma - pathology Humans Imidazoles - adverse effects Male Melanoma - drug therapy Melanoma - enzymology Melanoma - genetics Melanoma - secondary Middle Aged Oximes - adverse effects Predictive Value of Tests Protein Kinase Inhibitors - adverse effects Proto-Oncogene Proteins B-raf - antagonists & inhibitors Proto-Oncogene Proteins B-raf - genetics Proto-Oncogene Proteins B-raf - metabolism Skin - drug effects Skin - pathology Skin Neoplasms - drug therapy Skin Neoplasms - enzymology Skin Neoplasms - genetics Skin Neoplasms - pathology |
title | BRAF Inhibitor-Induced Antitumoral Granulomatous Dermatitis Eruption in Advanced Melanoma |
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