Brain tissue heterotopic in the adrenal gland in a child: a scarce case report
Abstract Heterotopic brain tissue is rare and has not been reported. Our center made the first report. 4 years and 2 months old Girl presented with a cystic mass in the right adrenal gland 2 weeks after right upper abdominal pain. The operation was successful, and the diagnosis was confirmed by post...
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Format: | Article |
Language: | English |
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BMC
2024-02-01
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Series: | BMC Pediatrics |
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Online Access: | https://doi.org/10.1186/s12887-023-04478-0 |
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author | Chenghao Zhanghuang Chengchuang Wu Junling Chen Fengming Ji Zhigang Yao Li Li Zhen Yang Haoyu Tang Kun Zhang Yu Hang Yucheng Xie Bing Yan |
author_facet | Chenghao Zhanghuang Chengchuang Wu Junling Chen Fengming Ji Zhigang Yao Li Li Zhen Yang Haoyu Tang Kun Zhang Yu Hang Yucheng Xie Bing Yan |
author_sort | Chenghao Zhanghuang |
collection | DOAJ |
description | Abstract Heterotopic brain tissue is rare and has not been reported. Our center made the first report. 4 years and 2 months old Girl presented with a cystic mass in the right adrenal gland 2 weeks after right upper abdominal pain. The operation was successful, and the diagnosis was confirmed by postoperative pathology. 6 months after the procedure, the incision healed well without recurrence. This case report has a detailed diagnosis and treatment process and satisfactory examination results. It can provide a reference for diagnosing and treating clinical HBT and reduce the risk of misdiagnosis and mistreatment. |
first_indexed | 2024-03-07T14:40:23Z |
format | Article |
id | doaj.art-096c3a47d5b149119e8ee802e6268499 |
institution | Directory Open Access Journal |
issn | 1471-2431 |
language | English |
last_indexed | 2024-03-07T14:40:23Z |
publishDate | 2024-02-01 |
publisher | BMC |
record_format | Article |
series | BMC Pediatrics |
spelling | doaj.art-096c3a47d5b149119e8ee802e62684992024-03-05T20:22:33ZengBMCBMC Pediatrics1471-24312024-02-012411510.1186/s12887-023-04478-0Brain tissue heterotopic in the adrenal gland in a child: a scarce case reportChenghao Zhanghuang0Chengchuang Wu1Junling Chen2Fengming Ji3Zhigang Yao4Li Li5Zhen Yang6Haoyu Tang7Kun Zhang8Yu Hang9Yucheng Xie10Bing Yan11Department of Urology, Kunming Children’s Hospital (Children’s Hospital affiliated to Kunming Medical University), Kunming, PR China Yunnan Province Clinical Research Center for Children’s Health and DiseaseDepartment of Urology, Kunming Children’s Hospital (Children’s Hospital affiliated to Kunming Medical University), Kunming, PR China Yunnan Province Clinical Research Center for Children’s Health and DiseaseLaboratory Medicine Department, Kunming Children’s Hospital (Children’s Hospital affiliated to Kunming Medical University)Department of Urology, Kunming Children’s Hospital (Children’s Hospital affiliated to Kunming Medical University), Kunming, PR China Yunnan Province Clinical Research Center for Children’s Health and DiseaseDepartment of Urology, Kunming Children’s Hospital (Children’s Hospital affiliated to Kunming Medical University), Kunming, PR China Yunnan Province Clinical Research Center for Children’s Health and DiseaseYunnan Clinical Medical Center for Pediatric Diseases; Yunnan Key Laboratory of Children’s Major Disease Research, Kunming Children’s Hospital (Children’s Hospital affiliated to Kunming Medical University)Department of Oncology; Kunming Children’s Solid Tumor Diagnosis and Treatment Center, Kunming Children’s Hospital (Children’s Hospital affiliated to Kunming Medical University)Department of Urology, Kunming Children’s Hospital (Children’s Hospital affiliated to Kunming Medical University), Kunming, PR China Yunnan Province Clinical Research Center for Children’s Health and DiseaseDepartment of Urology, Kunming Children’s Hospital (Children’s Hospital affiliated to Kunming Medical University), Kunming, PR China Yunnan Province Clinical Research Center for Children’s Health and DiseaseDepartment of Urology, Kunming Children’s Hospital (Children’s Hospital affiliated to Kunming Medical University), Kunming, PR China Yunnan Province Clinical Research Center for Children’s Health and DiseaseDepartment of Pathology, Kunming Children’s Hospital (Children’s Hospital affiliated to Kunming Medical University)Department of Urology, Kunming Children’s Hospital (Children’s Hospital affiliated to Kunming Medical University), Kunming, PR China Yunnan Province Clinical Research Center for Children’s Health and DiseaseAbstract Heterotopic brain tissue is rare and has not been reported. Our center made the first report. 4 years and 2 months old Girl presented with a cystic mass in the right adrenal gland 2 weeks after right upper abdominal pain. The operation was successful, and the diagnosis was confirmed by postoperative pathology. 6 months after the procedure, the incision healed well without recurrence. This case report has a detailed diagnosis and treatment process and satisfactory examination results. It can provide a reference for diagnosing and treating clinical HBT and reduce the risk of misdiagnosis and mistreatment.https://doi.org/10.1186/s12887-023-04478-0ChoristomaAdrenal gland neoplasmAdrenal glandsDiagnosisClinical pathologyTreatment |
spellingShingle | Chenghao Zhanghuang Chengchuang Wu Junling Chen Fengming Ji Zhigang Yao Li Li Zhen Yang Haoyu Tang Kun Zhang Yu Hang Yucheng Xie Bing Yan Brain tissue heterotopic in the adrenal gland in a child: a scarce case report BMC Pediatrics Choristoma Adrenal gland neoplasm Adrenal glands Diagnosis Clinical pathology Treatment |
title | Brain tissue heterotopic in the adrenal gland in a child: a scarce case report |
title_full | Brain tissue heterotopic in the adrenal gland in a child: a scarce case report |
title_fullStr | Brain tissue heterotopic in the adrenal gland in a child: a scarce case report |
title_full_unstemmed | Brain tissue heterotopic in the adrenal gland in a child: a scarce case report |
title_short | Brain tissue heterotopic in the adrenal gland in a child: a scarce case report |
title_sort | brain tissue heterotopic in the adrenal gland in a child a scarce case report |
topic | Choristoma Adrenal gland neoplasm Adrenal glands Diagnosis Clinical pathology Treatment |
url | https://doi.org/10.1186/s12887-023-04478-0 |
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