Malignant rhabdoid tumor beside benign skin mesenchymal neoplasm with myofibromatous features
Only a few reports of primary cutaneous rhabdoid tumors have been published. We describe the case of a 3‐month‐old female patient who developed a rhabdoid type cutaneous sareomatoid neoplasm in her upper back, close to a benign myofibromatous proliferation of infancy. The lesion was studied both by...
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| Veröffentlicht in: | Journal of cutaneous pathology 1999-11, Vol.26 (10), p.509-515 |
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| container_title | Journal of cutaneous pathology |
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| creator | García-Bustínduy, Marta Álvarez-Arguelles, Hugo Guimerá, Francisco García-Castro, Candelaria Sánchez-González, Rosalba Hernández, Norberto Diaz-Flores, Lucio García-Montelongo, Rafael |
| description | Only a few reports of primary cutaneous rhabdoid tumors have been published. We describe the case of a 3‐month‐old female patient who developed a rhabdoid type cutaneous sareomatoid neoplasm in her upper back, close to a benign myofibromatous proliferation of infancy. The lesion was studied both by light microscopy and immunohisto‐chemically. Flow cytometry was performed showing a DNA diploid profile of the malignant tumor. The pathological findings suggest a mesenchymal origin (hemangiopericytic or myofibroblastic type) for both tumors. The patient was surgically treated, but she died nine months later. |
| doi_str_mv | 10.1111/j.1600-0560.1999.tb01798.x |
| format | Article |
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We describe the case of a 3‐month‐old female patient who developed a rhabdoid type cutaneous sareomatoid neoplasm in her upper back, close to a benign myofibromatous proliferation of infancy. The lesion was studied both by light microscopy and immunohisto‐chemically. Flow cytometry was performed showing a DNA diploid profile of the malignant tumor. The pathological findings suggest a mesenchymal origin (hemangiopericytic or myofibroblastic type) for both tumors. The patient was surgically treated, but she died nine months later.</description><identifier>ISSN: 0303-6987</identifier><identifier>EISSN: 1600-0560</identifier><identifier>DOI: 10.1111/j.1600-0560.1999.tb01798.x</identifier><identifier>PMID: 10599942</identifier><identifier>CODEN: JCUPBN</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Biological and medical sciences ; Biomarkers, Tumor - analysis ; Cell Separation ; Dermatology ; DNA, Neoplasm - analysis ; Fatal Outcome ; Female ; Flow Cytometry ; Humans ; Immunoenzyme Techniques ; Infant ; Medical sciences ; Mesenchymoma - chemistry ; Mesenchymoma - genetics ; Mesenchymoma - pathology ; Mesenchymoma - surgery ; Neoplasms, Multiple Primary - chemistry ; Neoplasms, Multiple Primary - genetics ; Neoplasms, Multiple Primary - pathology ; Neoplasms, Multiple Primary - surgery ; Ploidies ; Rhabdoid Tumor - chemistry ; Rhabdoid Tumor - genetics ; Rhabdoid Tumor - pathology ; Rhabdoid Tumor - surgery ; Skin Neoplasms - chemistry ; Skin Neoplasms - genetics ; Skin Neoplasms - pathology ; Skin Neoplasms - surgery ; Tumors of the skin and soft tissue. 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We describe the case of a 3‐month‐old female patient who developed a rhabdoid type cutaneous sareomatoid neoplasm in her upper back, close to a benign myofibromatous proliferation of infancy. The lesion was studied both by light microscopy and immunohisto‐chemically. Flow cytometry was performed showing a DNA diploid profile of the malignant tumor. The pathological findings suggest a mesenchymal origin (hemangiopericytic or myofibroblastic type) for both tumors. The patient was surgically treated, but she died nine months later.</description><subject>Biological and medical sciences</subject><subject>Biomarkers, Tumor - analysis</subject><subject>Cell Separation</subject><subject>Dermatology</subject><subject>DNA, Neoplasm - analysis</subject><subject>Fatal Outcome</subject><subject>Female</subject><subject>Flow Cytometry</subject><subject>Humans</subject><subject>Immunoenzyme Techniques</subject><subject>Infant</subject><subject>Medical sciences</subject><subject>Mesenchymoma - chemistry</subject><subject>Mesenchymoma - genetics</subject><subject>Mesenchymoma - pathology</subject><subject>Mesenchymoma - surgery</subject><subject>Neoplasms, Multiple Primary - chemistry</subject><subject>Neoplasms, Multiple Primary - genetics</subject><subject>Neoplasms, Multiple Primary - pathology</subject><subject>Neoplasms, Multiple Primary - surgery</subject><subject>Ploidies</subject><subject>Rhabdoid Tumor - chemistry</subject><subject>Rhabdoid Tumor - genetics</subject><subject>Rhabdoid Tumor - pathology</subject><subject>Rhabdoid Tumor - surgery</subject><subject>Skin Neoplasms - chemistry</subject><subject>Skin Neoplasms - genetics</subject><subject>Skin Neoplasms - pathology</subject><subject>Skin Neoplasms - surgery</subject><subject>Tumors of the skin and soft tissue. Premalignant lesions</subject><issn>0303-6987</issn><issn>1600-0560</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkE1v1DAQhi1ERZeWv4AshLhlO05iJ-aAVFZ0iyi0h7ackOX4g_U2ThY7UXf_PV6yKlzxZSTPM6_HD0JvCMxJOmfrOWEAGVCWLjjn86EBUvF6vn2GZk-t52gGBRQZ43V1jF7GuAYgrGb0BTomQNNcmc_Qj6-ydT872Q04rGSje6fxMPo-4MZEp00qXerj-OA67E00nVrtvGxxZ_pNK6PHj25YYb_rrWtC7-XQjxFbI4cxmHiKjqxso3l1qCfo7uLT7eIyu7pefl6cX2WqZIxnhjNNFeWgcsXzomRWlcAUqFqWvCaNopIrYJBTmhNlLadNrXST16BtTbQuTtC7KXcT-l-jiYPwLirTtjKtOUbBeEErDjyB7ydQhT7GYKzYBOdl2AkCYi9XrMXeoNgbFHu54iBXbNPw68MrY-ON_md0spmAtwdARiVbG2SnXPzL5SQlsoR9mLBH15rdf2wgFnc39M8vsinAxcFsnwJkeBCsKioqvn9bivuP9zfLL5e34qL4DV6-p-0</recordid><startdate>199911</startdate><enddate>199911</enddate><creator>García-Bustínduy, Marta</creator><creator>Álvarez-Arguelles, Hugo</creator><creator>Guimerá, Francisco</creator><creator>García-Castro, Candelaria</creator><creator>Sánchez-González, Rosalba</creator><creator>Hernández, Norberto</creator><creator>Diaz-Flores, Lucio</creator><creator>García-Montelongo, Rafael</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>BSCLL</scope><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>7X8</scope></search><sort><creationdate>199911</creationdate><title>Malignant rhabdoid tumor beside benign skin mesenchymal neoplasm with myofibromatous features</title><author>García-Bustínduy, Marta ; Álvarez-Arguelles, Hugo ; Guimerá, Francisco ; García-Castro, Candelaria ; Sánchez-González, Rosalba ; Hernández, Norberto ; Diaz-Flores, Lucio ; García-Montelongo, Rafael</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4669-e96d5c590c2c92346fc406c0c8a4981bc5a9c06025521cff95b8cdb280df81dd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Biological and medical sciences</topic><topic>Biomarkers, Tumor - analysis</topic><topic>Cell Separation</topic><topic>Dermatology</topic><topic>DNA, Neoplasm - analysis</topic><topic>Fatal Outcome</topic><topic>Female</topic><topic>Flow Cytometry</topic><topic>Humans</topic><topic>Immunoenzyme Techniques</topic><topic>Infant</topic><topic>Medical sciences</topic><topic>Mesenchymoma - chemistry</topic><topic>Mesenchymoma - genetics</topic><topic>Mesenchymoma - pathology</topic><topic>Mesenchymoma - surgery</topic><topic>Neoplasms, Multiple Primary - chemistry</topic><topic>Neoplasms, Multiple Primary - genetics</topic><topic>Neoplasms, Multiple Primary - pathology</topic><topic>Neoplasms, Multiple Primary - surgery</topic><topic>Ploidies</topic><topic>Rhabdoid Tumor - chemistry</topic><topic>Rhabdoid Tumor - genetics</topic><topic>Rhabdoid Tumor - pathology</topic><topic>Rhabdoid Tumor - surgery</topic><topic>Skin Neoplasms - chemistry</topic><topic>Skin Neoplasms - genetics</topic><topic>Skin Neoplasms - pathology</topic><topic>Skin Neoplasms - surgery</topic><topic>Tumors of the skin and soft tissue. 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We describe the case of a 3‐month‐old female patient who developed a rhabdoid type cutaneous sareomatoid neoplasm in her upper back, close to a benign myofibromatous proliferation of infancy. The lesion was studied both by light microscopy and immunohisto‐chemically. Flow cytometry was performed showing a DNA diploid profile of the malignant tumor. The pathological findings suggest a mesenchymal origin (hemangiopericytic or myofibroblastic type) for both tumors. The patient was surgically treated, but she died nine months later.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>10599942</pmid><doi>10.1111/j.1600-0560.1999.tb01798.x</doi><tpages>7</tpages></addata></record> |
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| ispartof | Journal of cutaneous pathology, 1999-11, Vol.26 (10), p.509-515 |
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| subjects | Biological and medical sciences Biomarkers, Tumor - analysis Cell Separation Dermatology DNA, Neoplasm - analysis Fatal Outcome Female Flow Cytometry Humans Immunoenzyme Techniques Infant Medical sciences Mesenchymoma - chemistry Mesenchymoma - genetics Mesenchymoma - pathology Mesenchymoma - surgery Neoplasms, Multiple Primary - chemistry Neoplasms, Multiple Primary - genetics Neoplasms, Multiple Primary - pathology Neoplasms, Multiple Primary - surgery Ploidies Rhabdoid Tumor - chemistry Rhabdoid Tumor - genetics Rhabdoid Tumor - pathology Rhabdoid Tumor - surgery Skin Neoplasms - chemistry Skin Neoplasms - genetics Skin Neoplasms - pathology Skin Neoplasms - surgery Tumors of the skin and soft tissue. Premalignant lesions |
| title | Malignant rhabdoid tumor beside benign skin mesenchymal neoplasm with myofibromatous features |
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