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下肢血管球瘤一例最新综述及病例报告

A new case of lower extremity glomus tumor up-to date review and case report.

作者信息

Frumuseanu B, Balanescu R, Ulici A, Golumbeanu M, Barbu M, Orita V, Topor L

机构信息

Department of Pediatric Orthopedics, Grigore Alexandrescu Clinical Emergency Hospital for Children, Bucharest.

出版信息

J Med Life. 2012 Jun 12;5(2):211-4. Epub 2012 Jun 18.

PMID:22802895
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3391884/
Abstract

Glomus tumor (glomus cell tumor) is a rare, hamartomatous, usually benign neoplasm, whose cells resemble the modified smooth muscle cells of the normal glomus body. The diagnosis of a lower extremity is often delayed, due to the lack of awareness and low level of suspicion, by the treating physician. The glomus tumor (GT) often involves the nail beds. The unusual location of the lower extremity often leads to missed or delayed diagnosis and management. There is a paucy of information about GT in general, especially among orthopedic surgeons. The aim of this article is to make the surgical community more aware of this disease.

摘要

血管球瘤(glomous细胞瘤)是一种罕见的错构瘤,通常为良性肿瘤,其细胞类似于正常血管球体内经过修饰的平滑肌细胞。由于治疗医生缺乏认识且怀疑程度低,下肢血管球瘤的诊断常常被延误。血管球瘤(GT)常累及甲床。下肢这种不寻常的部位常常导致漏诊或诊断及治疗延误。总体而言,关于血管球瘤的信息很少,尤其是在骨科医生中。本文的目的是让外科界更多地了解这种疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d0d/3391884/1d791f0771b5/JMedLife-05-211-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d0d/3391884/3cda6c7a18ba/JMedLife-05-211-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d0d/3391884/7d8708364c57/JMedLife-05-211-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d0d/3391884/ea76dcf0080d/JMedLife-05-211-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d0d/3391884/c7b62df3b9da/JMedLife-05-211-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d0d/3391884/2bb5b2a71794/JMedLife-05-211-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d0d/3391884/1d791f0771b5/JMedLife-05-211-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d0d/3391884/3cda6c7a18ba/JMedLife-05-211-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d0d/3391884/7d8708364c57/JMedLife-05-211-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d0d/3391884/ea76dcf0080d/JMedLife-05-211-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d0d/3391884/c7b62df3b9da/JMedLife-05-211-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d0d/3391884/2bb5b2a71794/JMedLife-05-211-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d0d/3391884/1d791f0771b5/JMedLife-05-211-g006.jpg

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Four common glomulin mutations cause two thirds of glomuvenous malformations ("familial glomangiomas"): evidence for a founder effect.四种常见的球管蛋白突变导致三分之二的球静脉畸形(“家族性血管球瘤”):存在奠基者效应的证据。
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