Management of a Composite Pheochromocytoma (Pheochromocytoma/Neuroblastoma) in Adult Patient Recurring After Several Years: A Complex Case Report

被引：1

作者：

Magnier, Orlane ^{[1
,9
]}

Chabre, Olivier ^{[2
]}

Schiff, Isabelle ^{[3
]}

Sartelet, Herve ^{[4
,5
]}

Combaret, Valerie ^{[6
]}

Roux, Julie ^{[7
]}

Sturm, Nathalie ^{[8
]}

Berthozat, Claudine ^{[1
]}

Pavillet, Julien ^{[1
]}

Plantaz, Dominique ^{[3
]}

机构：

[1] Grenoble Alpes Univ Hosp, Dept Med Oncol Canc & Blood Dis, Grenoble, France

[2] Grenoble Alpes Univ Hosp, Dept Endocrinol, Grenoble, France

[3] Grenoble Alpes Univ Hosp, Dept Pediat Oncoimmunohematol, Grenoble, France

[4] Grenoble Alpes Univ Hosp, Dept Pathol, Grenoble, France

[5] Univ Lorraine, Nancy Univ Hosp, Dept Biopathol, Nancy, France

[6] Leon Berard Ctr, Translat Res Lab, Lyon, France

[7] Grenoble Alpes Univ Hosp, Dept Nucl Med, Grenoble, France

[8] Grenoble Alpes Univ Hosp, Dept Biopathol, Grenoble, France

[9] Grenoble Alpes Univ Hosp, Dept Med Oncol Canc & Blood Dis, F-38043 Grenoble, France

来源：

JOURNAL OF ADOLESCENT AND YOUNG ADULT ONCOLOGY | 2023年 / 12卷 / 04期

关键词：

neuroblastoma; composite pheochromocytoma; adrenal tumor; adult; peripheric neuroblastic tumor; case report; NEUROBLASTOMA; TUMORS; CGH;

D O I：

10.1089/jayao.2022.0059

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

Pheochromocytoma/neuroblastoma composite tumors are rare entities for which little is known. We report an atypical case of a 39-year-old man with secondary bone locations of a composite tumor, 7 years after resection of adrenal neuroblastoma, with constitutional alteration of SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin, subfamily A, member 4 whose role is unknown. The diagnosis of a peripheral neuroblastic tumor in adulthood is difficult and even more so when it is a composite tumor. In the absence of a standard of care, management is varied and discussions about treatment modalities for these patients are complex.

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收藏

页码：604 / 610

页数：7

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