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Incidental diagnosis of a rare endobronchial schwannoma in a 7-year-old girl: A case report
Schwannomas are nerve sheath tumors that arise from Schwann cells and are mainly benign. The likelihood of endobronchial schwannoma amongst all intrapulmonary tumors is up to 0.2% and mainly presents late. This study described a pediatric endobronchial schwannomas case discovered incidentally during...
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Published in: | Radiology case reports 2022-10, Vol.17 (10), p.4043-4045 |
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description | Schwannomas are nerve sheath tumors that arise from Schwann cells and are mainly benign. The likelihood of endobronchial schwannoma amongst all intrapulmonary tumors is up to 0.2% and mainly presents late. This study described a pediatric endobronchial schwannomas case discovered incidentally during rigid bronchoscopy. This case is uncommon, and its report can help physicians diagnose the same cases. The case was a 7-year-old girl presenting with fever and cough who had no history of pulmonary disease or relevant family history. Physical examination, chest radiography, CT scan, and bronchoscopy were performed on the patient. A biopsy was taken from the observed mass obstructing the bronchus during bronchoscopy. The mass was resected. Pathology revealed low-grade spindle cell neoplasm and confirmed schwannoma in immunohistochemistry. Endobronchial schwannomas can happen in children presenting with simple symptoms. For benign lesions, the prognosis is generally good. Due to the slow growth of these tumors and the potential for recurrence after resection, long-term follow-up may be needed. |
doi_str_mv | 10.1016/j.radcr.2022.07.115 |
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The likelihood of endobronchial schwannoma amongst all intrapulmonary tumors is up to 0.2% and mainly presents late. This study described a pediatric endobronchial schwannomas case discovered incidentally during rigid bronchoscopy. This case is uncommon, and its report can help physicians diagnose the same cases. The case was a 7-year-old girl presenting with fever and cough who had no history of pulmonary disease or relevant family history. Physical examination, chest radiography, CT scan, and bronchoscopy were performed on the patient. A biopsy was taken from the observed mass obstructing the bronchus during bronchoscopy. The mass was resected. Pathology revealed low-grade spindle cell neoplasm and confirmed schwannoma in immunohistochemistry. Endobronchial schwannomas can happen in children presenting with simple symptoms. For benign lesions, the prognosis is generally good. 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The likelihood of endobronchial schwannoma amongst all intrapulmonary tumors is up to 0.2% and mainly presents late. This study described a pediatric endobronchial schwannomas case discovered incidentally during rigid bronchoscopy. This case is uncommon, and its report can help physicians diagnose the same cases. The case was a 7-year-old girl presenting with fever and cough who had no history of pulmonary disease or relevant family history. Physical examination, chest radiography, CT scan, and bronchoscopy were performed on the patient. A biopsy was taken from the observed mass obstructing the bronchus during bronchoscopy. The mass was resected. Pathology revealed low-grade spindle cell neoplasm and confirmed schwannoma in immunohistochemistry. Endobronchial schwannomas can happen in children presenting with simple symptoms. For benign lesions, the prognosis is generally good. Due to the slow growth of these tumors and the potential for recurrence after resection, long-term follow-up may be needed.</description><subject>Case Report</subject><subject>Endobronchial</subject><subject>Schwannomas</subject><issn>1930-0433</issn><issn>1930-0433</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9kctqHDEQRZsQEz-SL8hGP9BtvVpqBRIwxo4HDNk4qyxEtVSa0dAjDdLEwX8f2RNCvMmqiqq6B-rervvI6MAoU5fboYB3ZeCU84HqgbHxTXfGjKA9lUK8_ac_7c5r3VKqxKTZu-5UKCqVZvqs-7FKLnpMB1iIj7BOucZKciBAChQkmHyeS05uE9tFdZtfkFLeAYmpnej-CaH0efFkHcvyiVwRBxVJwX0uh_fdSYCl4oc_9aL7fnvzcH3X33_7urq-uu-dEHLslZ-cVsJIHRA4lyi9BMMC53RCJowxcvQmMD7p0UmhZ5BMIRjtmBJUT-KiWx25PsPW7kvcQXmyGaJ9GeSytlAO0S1oRwQhQlAqjEoGORsGLkyj4jNKxzRtrC9H1v7nvEPvmjMFllfQ15sUN3adH62RnFHDGkAcAa7kWguGv1pG7XNudmtfcrPPuVmqbcutqT4fVdh8eoxYbHURk0MfC7pDeyT-V_8bQKmgKQ</recordid><startdate>20221001</startdate><enddate>20221001</enddate><creator>Jahromi, Mehdi Ghaderian</creator><creator>Yakhdani, Abdolrahim Sadeghi</creator><creator>Saeedi-Moghadam, Mahdi</creator><creator>Iranpour, Pooya</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-6652-2053</orcidid></search><sort><creationdate>20221001</creationdate><title>Incidental diagnosis of a rare endobronchial schwannoma in a 7-year-old girl: A case report</title><author>Jahromi, Mehdi Ghaderian ; Yakhdani, Abdolrahim Sadeghi ; Saeedi-Moghadam, Mahdi ; Iranpour, Pooya</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3345-6d8c763947fea224e4d4a91f2208e1399945d9f12875c437ba416ea97c1630783</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Case Report</topic><topic>Endobronchial</topic><topic>Schwannomas</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jahromi, Mehdi Ghaderian</creatorcontrib><creatorcontrib>Yakhdani, Abdolrahim Sadeghi</creatorcontrib><creatorcontrib>Saeedi-Moghadam, Mahdi</creatorcontrib><creatorcontrib>Iranpour, Pooya</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Radiology case reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jahromi, Mehdi Ghaderian</au><au>Yakhdani, Abdolrahim Sadeghi</au><au>Saeedi-Moghadam, Mahdi</au><au>Iranpour, Pooya</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Incidental diagnosis of a rare endobronchial schwannoma in a 7-year-old girl: A case report</atitle><jtitle>Radiology case reports</jtitle><date>2022-10-01</date><risdate>2022</risdate><volume>17</volume><issue>10</issue><spage>4043</spage><epage>4045</epage><pages>4043-4045</pages><issn>1930-0433</issn><eissn>1930-0433</eissn><abstract>Schwannomas are nerve sheath tumors that arise from Schwann cells and are mainly benign. The likelihood of endobronchial schwannoma amongst all intrapulmonary tumors is up to 0.2% and mainly presents late. This study described a pediatric endobronchial schwannomas case discovered incidentally during rigid bronchoscopy. This case is uncommon, and its report can help physicians diagnose the same cases. The case was a 7-year-old girl presenting with fever and cough who had no history of pulmonary disease or relevant family history. Physical examination, chest radiography, CT scan, and bronchoscopy were performed on the patient. A biopsy was taken from the observed mass obstructing the bronchus during bronchoscopy. The mass was resected. Pathology revealed low-grade spindle cell neoplasm and confirmed schwannoma in immunohistochemistry. Endobronchial schwannomas can happen in children presenting with simple symptoms. For benign lesions, the prognosis is generally good. Due to the slow growth of these tumors and the potential for recurrence after resection, long-term follow-up may be needed.</abstract><pub>Elsevier Inc</pub><pmid>36046717</pmid><doi>10.1016/j.radcr.2022.07.115</doi><tpages>3</tpages><orcidid>https://orcid.org/0000-0001-6652-2053</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Case Report Endobronchial Schwannomas |
title | Incidental diagnosis of a rare endobronchial schwannoma in a 7-year-old girl: A case report |
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