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Case report: neonatal giant forehead hemangiopericytoma with a 5-year follow-up
RATIONALE: Hemangiopericytoma (HPC) is a rare pediatric neoplasm with a high risk of bleeding, aggressive growth and high early relapse rates. Surgical excision remains the mainstream treatment, while the functions of chemotherapy and radiotherapy remain controversial. In particular, an infantile gi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6882637/ https://www.ncbi.nlm.nih.gov/pubmed/31764783 http://dx.doi.org/10.1097/MD.0000000000017888 |
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author | Peng, AiJun Zhang, LiBing Zhao, Hai Zhou, LiangXue |
author_facet | Peng, AiJun Zhang, LiBing Zhao, Hai Zhou, LiangXue |
author_sort | Peng, AiJun |
collection | PubMed |
description | RATIONALE: Hemangiopericytoma (HPC) is a rare pediatric neoplasm with a high risk of bleeding, aggressive growth and high early relapse rates. Surgical excision remains the mainstream treatment, while the functions of chemotherapy and radiotherapy remain controversial. In particular, an infantile giant extracranial HPC located in the forehead has never been reported. PATIENT CONCERNS: A 3-day-old girl was delivered normally with a giant tumor localized mainly in the right frontal region. The surface of the mass was filled with vascularity. DIAGNOSIS: According to the results of imaging and pathological examinations, the diagnosis was HPC grade II. INTERVENTIONS: Gross total resection of the tumor and the invading partial frontal bone followed by skin scalp reconstruction was carried out without any blood transfusion. OUTCOMES: No recurrence was identified during 5 years of follow-up. And better outcomes can be achieved without adjuvant therapy. LESSONS: Multimodality imaging and a collaborative multidisciplinary approach are indispensable for the successful surgical management of infantile HPC, especially for giant tumors and their potential risk of life-threatening bleeding. Gross total resection is the optimal option for infantile HPC, and even without adjuvant therapy, it achieves better outcomes. |
format | Online Article Text |
id | pubmed-6882637 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-68826372020-01-22 Case report: neonatal giant forehead hemangiopericytoma with a 5-year follow-up Peng, AiJun Zhang, LiBing Zhao, Hai Zhou, LiangXue Medicine (Baltimore) 6200 RATIONALE: Hemangiopericytoma (HPC) is a rare pediatric neoplasm with a high risk of bleeding, aggressive growth and high early relapse rates. Surgical excision remains the mainstream treatment, while the functions of chemotherapy and radiotherapy remain controversial. In particular, an infantile giant extracranial HPC located in the forehead has never been reported. PATIENT CONCERNS: A 3-day-old girl was delivered normally with a giant tumor localized mainly in the right frontal region. The surface of the mass was filled with vascularity. DIAGNOSIS: According to the results of imaging and pathological examinations, the diagnosis was HPC grade II. INTERVENTIONS: Gross total resection of the tumor and the invading partial frontal bone followed by skin scalp reconstruction was carried out without any blood transfusion. OUTCOMES: No recurrence was identified during 5 years of follow-up. And better outcomes can be achieved without adjuvant therapy. LESSONS: Multimodality imaging and a collaborative multidisciplinary approach are indispensable for the successful surgical management of infantile HPC, especially for giant tumors and their potential risk of life-threatening bleeding. Gross total resection is the optimal option for infantile HPC, and even without adjuvant therapy, it achieves better outcomes. Wolters Kluwer Health 2019-11-22 /pmc/articles/PMC6882637/ /pubmed/31764783 http://dx.doi.org/10.1097/MD.0000000000017888 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | 6200 Peng, AiJun Zhang, LiBing Zhao, Hai Zhou, LiangXue Case report: neonatal giant forehead hemangiopericytoma with a 5-year follow-up |
title | Case report: neonatal giant forehead hemangiopericytoma with a 5-year follow-up |
title_full | Case report: neonatal giant forehead hemangiopericytoma with a 5-year follow-up |
title_fullStr | Case report: neonatal giant forehead hemangiopericytoma with a 5-year follow-up |
title_full_unstemmed | Case report: neonatal giant forehead hemangiopericytoma with a 5-year follow-up |
title_short | Case report: neonatal giant forehead hemangiopericytoma with a 5-year follow-up |
title_sort | case report: neonatal giant forehead hemangiopericytoma with a 5-year follow-up |
topic | 6200 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6882637/ https://www.ncbi.nlm.nih.gov/pubmed/31764783 http://dx.doi.org/10.1097/MD.0000000000017888 |
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