Hemangioma of the rib: a rare case report and literature review-Reference-Cited by-同舟云学术

Hemangioma of the rib: a rare case report and literature review

Published:2017-08-10 Issue:1 Volume:12 Page:257-260
ISSN:2391-5463
Container-title:Open Medicine
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Author:

Zhu You-cai¹,Lin Xue-ping²,Lu Yan³,Wang Wen-xian⁴,Du Kai-qi⁵,Ye Xiao-qian⁶,Zong Chong⁷,Xu Chun-wei⁸

Affiliation:

1. Department of Thoracic Disease Center, Zhejiang Rongjun Hospital, People′s Republic of China, No.589 Central West Road, Jiaxing, Zhejiang Province People‘s Republic of China

2. Department of Pathology, Jiaxing University College of Medicine, JiaxingZhejiang 314000, People′s Republic of China

3. Department of Internal Medicine, Jiaxing Second Hospital, 314000, Jiaxing People′s Republic of China

4. Department of Chemotherapy, Zhejiang Cancer Hospital, HangzhouZhejiang 310022, People′s Republic of China

5. Department of Thoracic Disease Center, Zhejiang Rongjun Hospital, JiaxingZhejiang 314000, People′s Republic of China

6. Department of Pathology, Chinese People′s Armed Police Force, Zhejiang Corps Hospital, 314000, Zhejiang People′s Republic of China

7. Department of Cardiothoracic Surgery, The First Affiliated Hospital of Medical School of Zhejiang University, 310003, Zhejiang People′s Republic of China

8. Department of Pathology, Fujian Provincial Cancer Hospital, Fujian Medical University Cancer Hospital, FuzhouFujian 350014, People′s Republic of China

Abstract

AbstractHemangiomas of the rib are extremely rare benign neoplasm. Here we present a case in a 47-year-old female, detected by chest X-ray and underwent a surgical resection. Histologically, the tumor was composed of a homogeneous conglomerate, irregular, thin walled and dilated blood vessels containing red blood cells, supported by fibrous stroma and intermingled to regular bone trabeculae. The postoperative courses were uneventful, and there was no recurrence during 64 months follow-up.

Publisher

Walter de Gruyter GmbH

Subject

General Medicine

Link

https://www.degruyter.com/document/doi/10.1515/med-2017-0038/pdf

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