| Literature DB >> 32042691 |
Weibo Xu1,2, Yanqing Qu3, Wen Shi1, Ben Ma1,2, Hongyi Jiang1,2, Yu Wang1,2, Ning Qu1,2, Yongxue Zhu1,2.
Abstract
Bone brown tumors secondary to primary hyperparathyroidism (PHPT) are rare and only around 2-5% of PHPT patients have multiple bone brown tumor lesions, which are also uncommon in literatures. We found a female patient who got misdiagnosis of multiple malignant bone tumors in our clinical work, she was eventually diagnosed as a brown tumor secondary to hyperparathyroidism. This article records the diagnosis and treatment process, and summarizes similar case reports in the past decade to provide experience in diagnosis and treatment of similar cases that may occur in the future. 2019 Gland Surgery. All rights reserved.Entities:
Keywords: Bone brown tumor; case report; diagnosis and treatment; literature review; primary hyperparathyroidism (PHPT)
Year: 2019 PMID: 32042691 PMCID: PMC6989901 DOI: 10.21037/gs.2019.11.14
Source DB: PubMed Journal: Gland Surg ISSN: 2227-684X