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囊性水瘤切除术后19年，胸壁出现海绵状淋巴管瘤。

Cavernous lymphangioma arising in the chest wall 19 years after excision of a cystic hygroma.

作者信息

Lee Woo Surng, Kim Yo Han, Chee Hyun Keun, Lee Song Am, Kim Jong Duk, Kim Dong Chan

机构信息

Department of Thoracic and Cardiovascular Surgery, School of Medicine, Konkuk University, Korea.

出版信息

Korean J Thorac Cardiovasc Surg. 2011 Oct;44(5):380-2. doi: 10.5090/kjtcs.2011.44.5.380. Epub 2011 Oct 6.

DOI:10.5090/kjtcs.2011.44.5.380
PMID:22263194
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3249346/
Abstract

Lymphangioma is a congenital malformation of the lymphatic system and is thought to result from the failure of the lymphatic system to connect with the venous system. Lymphangioma of the chest wall is a very rare disease entity, and only a few cases have ever been documented in the literature. To the best of our knowledge, there have been few cases of recurrent cavernous lymphangioma after surgical excision of a cystic hygroma on the same side of the chest wall. Here, we report a case of a cavernous lymphangioma of the chest wall in a patient who had undergone surgical excision of a cystic hygroma 19 years earlier.

摘要

淋巴管瘤是一种先天性淋巴系统畸形，被认为是由于淋巴系统未能与静脉系统相连所致。胸壁淋巴管瘤是一种非常罕见的疾病实体，文献中仅有少数病例记载。据我们所知，在胸壁同一侧的囊状水瘤手术切除后复发性海绵状淋巴管瘤的病例很少。在此，我们报告一例胸壁海绵状淋巴管瘤患者，该患者19年前曾接受过囊状水瘤的手术切除。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4884/3249346/301b0cac5c1d/kjtcs-44-380-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4884/3249346/19b43867fbe1/kjtcs-44-380-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4884/3249346/301b0cac5c1d/kjtcs-44-380-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4884/3249346/19b43867fbe1/kjtcs-44-380-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4884/3249346/301b0cac5c1d/kjtcs-44-380-g002.jpg

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