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Pulmonary anthracosis mimicking lung metastases in pediatric rhabdomyosarcoma
Although childhood rhabdomyosarcoma typically metastasizes to lungs, various processes may mimic metastatic etiology. Described herein is the case of an 8½‐year‐old boy with orbital embryonal rhabdomyosarcoma (RME) in whom three small foci were detected within both lungs on computed tomography. The...
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Published in: | Pediatrics international 2016-10, Vol.58 (10), p.1066-1068 |
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creator | Karpinsky, Gabrielle Krawczyk, Malgorzata Anna Fatyga, Aleksandra Izycka‐Swieszewska, Ewa Dubaniewicz‐Wybieralska, Miroslawa Szmyd, Dagmara Luboch‐Furmanczyk, Monika Bien, Ewa |
description | Although childhood rhabdomyosarcoma typically metastasizes to lungs, various processes may mimic metastatic etiology. Described herein is the case of an 8½‐year‐old boy with orbital embryonal rhabdomyosarcoma (RME) in whom three small foci were detected within both lungs on computed tomography. The lesion number and size, however, did not fulfil the Cooperative Weichteilsarkom Study Group 2006 protocol criteria for lung metastasis. Chemotherapy for localized RME produced primary tumor regression and vanishing of the left lung lesion. Two lesions in the right lung remained unchanged. On thoracoscopy multiple minute nodules disseminated in both lungs were detected. Histopathology excluded RME spread but indicated anthracosis in the lung parenchyma and intrapulmonary lymph nodes. Heavy smoking by parents and previous home furnace combustion appeared to be predisposing factors. Uncommon non‐malignant intrapulmonary diseases, including anthracosis, should be considered when staging pediatric cancer. |
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Described herein is the case of an 8½‐year‐old boy with orbital embryonal rhabdomyosarcoma (RME) in whom three small foci were detected within both lungs on computed tomography. The lesion number and size, however, did not fulfil the Cooperative Weichteilsarkom Study Group 2006 protocol criteria for lung metastasis. Chemotherapy for localized RME produced primary tumor regression and vanishing of the left lung lesion. Two lesions in the right lung remained unchanged. On thoracoscopy multiple minute nodules disseminated in both lungs were detected. Histopathology excluded RME spread but indicated anthracosis in the lung parenchyma and intrapulmonary lymph nodes. Heavy smoking by parents and previous home furnace combustion appeared to be predisposing factors. Uncommon non‐malignant intrapulmonary diseases, including anthracosis, should be considered when staging pediatric cancer.</description><identifier>ISSN: 1328-8067</identifier><identifier>EISSN: 1442-200X</identifier><identifier>DOI: 10.1111/ped.13058</identifier><identifier>PMID: 27592612</identifier><language>eng</language><publisher>Australia: Blackwell Publishing Ltd</publisher><subject>Anthracosis - complications ; Anthracosis - diagnosis ; benign lung lesion ; Biopsy ; Cancer ; Chemotherapy ; Child ; Children ; Computed tomography ; Diagnosis, Differential ; embryonal rhabdomyosarcoma ; Etiology ; Histopathology ; Humans ; Lesions ; Lung - diagnostic imaging ; Lung cancer ; lung metastasis ; Lung Neoplasms - diagnosis ; Lung nodules ; Lungs ; Lymph nodes ; Magnetic Resonance Imaging ; Male ; Metastases ; Metastasis ; Mimicry ; Orbital Neoplasms - complications ; Orbital Neoplasms - diagnosis ; Parenchyma ; Pediatrics ; pulmonary anthracosis ; Rhabdomyosarcoma ; Rhabdomyosarcoma, Embryonal - complications ; Rhabdomyosarcoma, Embryonal - diagnosis ; Smoking ; Tomography ; Tomography, X-Ray Computed</subject><ispartof>Pediatrics international, 2016-10, Vol.58 (10), p.1066-1068</ispartof><rights>2016 Japan Pediatric Society</rights><rights>2016 Japan Pediatric Society.</rights><rights>Copyright © 2016 Japan Pediatric Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3658-b1fc47a5a36248bfebab75a41e7722ea54932a508a4c832028f8c5b5df996733</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27592612$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Karpinsky, Gabrielle</creatorcontrib><creatorcontrib>Krawczyk, Malgorzata Anna</creatorcontrib><creatorcontrib>Fatyga, Aleksandra</creatorcontrib><creatorcontrib>Izycka‐Swieszewska, Ewa</creatorcontrib><creatorcontrib>Dubaniewicz‐Wybieralska, Miroslawa</creatorcontrib><creatorcontrib>Szmyd, Dagmara</creatorcontrib><creatorcontrib>Luboch‐Furmanczyk, Monika</creatorcontrib><creatorcontrib>Bien, Ewa</creatorcontrib><title>Pulmonary anthracosis mimicking lung metastases in pediatric rhabdomyosarcoma</title><title>Pediatrics international</title><addtitle>Pediatr Int</addtitle><description>Although childhood rhabdomyosarcoma typically metastasizes to lungs, various processes may mimic metastatic etiology. Described herein is the case of an 8½‐year‐old boy with orbital embryonal rhabdomyosarcoma (RME) in whom three small foci were detected within both lungs on computed tomography. The lesion number and size, however, did not fulfil the Cooperative Weichteilsarkom Study Group 2006 protocol criteria for lung metastasis. Chemotherapy for localized RME produced primary tumor regression and vanishing of the left lung lesion. Two lesions in the right lung remained unchanged. On thoracoscopy multiple minute nodules disseminated in both lungs were detected. Histopathology excluded RME spread but indicated anthracosis in the lung parenchyma and intrapulmonary lymph nodes. Heavy smoking by parents and previous home furnace combustion appeared to be predisposing factors. Uncommon non‐malignant intrapulmonary diseases, including anthracosis, should be considered when staging pediatric cancer.</description><subject>Anthracosis - complications</subject><subject>Anthracosis - diagnosis</subject><subject>benign lung lesion</subject><subject>Biopsy</subject><subject>Cancer</subject><subject>Chemotherapy</subject><subject>Child</subject><subject>Children</subject><subject>Computed tomography</subject><subject>Diagnosis, Differential</subject><subject>embryonal rhabdomyosarcoma</subject><subject>Etiology</subject><subject>Histopathology</subject><subject>Humans</subject><subject>Lesions</subject><subject>Lung - diagnostic imaging</subject><subject>Lung cancer</subject><subject>lung metastasis</subject><subject>Lung Neoplasms - diagnosis</subject><subject>Lung nodules</subject><subject>Lungs</subject><subject>Lymph nodes</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Mimicry</subject><subject>Orbital Neoplasms - complications</subject><subject>Orbital Neoplasms - diagnosis</subject><subject>Parenchyma</subject><subject>Pediatrics</subject><subject>pulmonary anthracosis</subject><subject>Rhabdomyosarcoma</subject><subject>Rhabdomyosarcoma, Embryonal - complications</subject><subject>Rhabdomyosarcoma, Embryonal - diagnosis</subject><subject>Smoking</subject><subject>Tomography</subject><subject>Tomography, X-Ray Computed</subject><issn>1328-8067</issn><issn>1442-200X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNp9kUtLxDAUhYMoOj4W_gEpuNFFZ_Js06WMT1CcxSzchdtMqhmbZkxaZP690dGNoIeQG8LHuZdzETomeEySJiuzGBOGhdxCI8I5zSnGT9vpzajMJS7KPbQf4xJjLEvJd9EeLUVFC0JH6GE2tM53ENYZdP1LAO2jjZmzzupX2z1n7ZAuZ3qI6ZiY2S5L7Sz0weosvEC98G7tIwTtHRyinQbaaI6-6wGaX1_Np7f5_ePN3fTiPtesEDKvSaN5CQJYQbmsG1NDXQrgxJQlpQYErxgFgSVwLRnFVDZSi1osmqoqSsYO0NnGdhX822Bir5yN2rQtdMYPURHJC46LitCEnv5Cl34IXRpOUVIkiRTYfxSRjAtZUfxJnW8oHXyMwTRqFaxL0SmC1eciVEpGfS0isSffjkPt0u8P-ZN8AiYb4N22Zv23k5pdXW4sPwDXFJEM</recordid><startdate>201610</startdate><enddate>201610</enddate><creator>Karpinsky, Gabrielle</creator><creator>Krawczyk, Malgorzata Anna</creator><creator>Fatyga, Aleksandra</creator><creator>Izycka‐Swieszewska, Ewa</creator><creator>Dubaniewicz‐Wybieralska, Miroslawa</creator><creator>Szmyd, Dagmara</creator><creator>Luboch‐Furmanczyk, Monika</creator><creator>Bien, Ewa</creator><general>Blackwell Publishing Ltd</general><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>7TK</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope></search><sort><creationdate>201610</creationdate><title>Pulmonary anthracosis mimicking lung metastases in pediatric rhabdomyosarcoma</title><author>Karpinsky, Gabrielle ; Krawczyk, Malgorzata Anna ; Fatyga, Aleksandra ; Izycka‐Swieszewska, Ewa ; Dubaniewicz‐Wybieralska, Miroslawa ; Szmyd, Dagmara ; Luboch‐Furmanczyk, Monika ; Bien, Ewa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3658-b1fc47a5a36248bfebab75a41e7722ea54932a508a4c832028f8c5b5df996733</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Anthracosis - complications</topic><topic>Anthracosis - diagnosis</topic><topic>benign lung lesion</topic><topic>Biopsy</topic><topic>Cancer</topic><topic>Chemotherapy</topic><topic>Child</topic><topic>Children</topic><topic>Computed tomography</topic><topic>Diagnosis, Differential</topic><topic>embryonal rhabdomyosarcoma</topic><topic>Etiology</topic><topic>Histopathology</topic><topic>Humans</topic><topic>Lesions</topic><topic>Lung - diagnostic imaging</topic><topic>Lung cancer</topic><topic>lung metastasis</topic><topic>Lung Neoplasms - diagnosis</topic><topic>Lung nodules</topic><topic>Lungs</topic><topic>Lymph nodes</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Mimicry</topic><topic>Orbital Neoplasms - complications</topic><topic>Orbital Neoplasms - diagnosis</topic><topic>Parenchyma</topic><topic>Pediatrics</topic><topic>pulmonary anthracosis</topic><topic>Rhabdomyosarcoma</topic><topic>Rhabdomyosarcoma, Embryonal - complications</topic><topic>Rhabdomyosarcoma, Embryonal - diagnosis</topic><topic>Smoking</topic><topic>Tomography</topic><topic>Tomography, X-Ray Computed</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Karpinsky, Gabrielle</creatorcontrib><creatorcontrib>Krawczyk, Malgorzata Anna</creatorcontrib><creatorcontrib>Fatyga, Aleksandra</creatorcontrib><creatorcontrib>Izycka‐Swieszewska, Ewa</creatorcontrib><creatorcontrib>Dubaniewicz‐Wybieralska, Miroslawa</creatorcontrib><creatorcontrib>Szmyd, Dagmara</creatorcontrib><creatorcontrib>Luboch‐Furmanczyk, Monika</creatorcontrib><creatorcontrib>Bien, Ewa</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><jtitle>Pediatrics international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Karpinsky, Gabrielle</au><au>Krawczyk, Malgorzata Anna</au><au>Fatyga, Aleksandra</au><au>Izycka‐Swieszewska, Ewa</au><au>Dubaniewicz‐Wybieralska, Miroslawa</au><au>Szmyd, Dagmara</au><au>Luboch‐Furmanczyk, Monika</au><au>Bien, Ewa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pulmonary anthracosis mimicking lung metastases in pediatric rhabdomyosarcoma</atitle><jtitle>Pediatrics international</jtitle><addtitle>Pediatr Int</addtitle><date>2016-10</date><risdate>2016</risdate><volume>58</volume><issue>10</issue><spage>1066</spage><epage>1068</epage><pages>1066-1068</pages><issn>1328-8067</issn><eissn>1442-200X</eissn><abstract>Although childhood rhabdomyosarcoma typically metastasizes to lungs, various processes may mimic metastatic etiology. Described herein is the case of an 8½‐year‐old boy with orbital embryonal rhabdomyosarcoma (RME) in whom three small foci were detected within both lungs on computed tomography. The lesion number and size, however, did not fulfil the Cooperative Weichteilsarkom Study Group 2006 protocol criteria for lung metastasis. Chemotherapy for localized RME produced primary tumor regression and vanishing of the left lung lesion. Two lesions in the right lung remained unchanged. On thoracoscopy multiple minute nodules disseminated in both lungs were detected. Histopathology excluded RME spread but indicated anthracosis in the lung parenchyma and intrapulmonary lymph nodes. Heavy smoking by parents and previous home furnace combustion appeared to be predisposing factors. Uncommon non‐malignant intrapulmonary diseases, including anthracosis, should be considered when staging pediatric cancer.</abstract><cop>Australia</cop><pub>Blackwell Publishing Ltd</pub><pmid>27592612</pmid><doi>10.1111/ped.13058</doi><tpages>3</tpages></addata></record> |
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subjects | Anthracosis - complications Anthracosis - diagnosis benign lung lesion Biopsy Cancer Chemotherapy Child Children Computed tomography Diagnosis, Differential embryonal rhabdomyosarcoma Etiology Histopathology Humans Lesions Lung - diagnostic imaging Lung cancer lung metastasis Lung Neoplasms - diagnosis Lung nodules Lungs Lymph nodes Magnetic Resonance Imaging Male Metastases Metastasis Mimicry Orbital Neoplasms - complications Orbital Neoplasms - diagnosis Parenchyma Pediatrics pulmonary anthracosis Rhabdomyosarcoma Rhabdomyosarcoma, Embryonal - complications Rhabdomyosarcoma, Embryonal - diagnosis Smoking Tomography Tomography, X-Ray Computed |
title | Pulmonary anthracosis mimicking lung metastases in pediatric rhabdomyosarcoma |
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