Subcutaneous Cavernous Haemangioma in a Patient with Klippel-Trenaunay Syndrome: A Case Report

被引：0

作者：

Liu, Yixin ^{[1
]}

Liu, Ling ^{[1
]}

Liu, Xia ^{[1
]}

Liu, Rengui ^{[2
]}

Cui, Chunmao ^{[1
]}

Cao, Huaize ^{[1
]}

机构：

[1] Dali Univ, Affiliated Hosp 1, Dept Radiol, Dali, Yunnan, Peoples R China

[2] Dali Univ, Affiliated Hosp 1, Dept Vasc Surg, Dali, Yunnan, Peoples R China

来源：

CURRENT MEDICAL IMAGING | 2024年 / 20卷

关键词：

Klippel-Trenaunay syndrome; Limb hypertrophy; Port wine stain; Vascular malformation; Blood vessels; Haemangioma; MANAGEMENT;

D O I：

10.2174/0115734056251193231016042812

中图分类号：

R8 [特种医学]; R445 [影像诊断学];

学科分类号：

1002 ; 100207 ; 1009 ;

摘要：

Background: Klippel-Trenaunay syndrome (KTS) is a rare congenital disease that mainly involves blood vessels and is characterized by the presence of capillary malformations (port wine stains), varicose veins, soft tissue and/or bone hypertrophy.Case Presentation: We report a 28-year-old man who was diagnosed 20 years ago with Klippel-Trenaunay syndrome. Approximately 3 years ago, he found enlarged masses on both upper extremities and a new dark red mass that was pathologically diagnosed as cavernous haemangioma appeared on the right index finger.Conclusion: KTS is a rare and potentially multisystem disease requiring multidisciplinary management for which imaging examination is an important auxiliary diagnostic method. Various complications may occur during its development, so regular follow-up is required to prevent serious accidents.

引用

页数：6

共 16 条

[1] Imaging Findings of Klippel-Trenaunay Syndrome
Abdel Razek, Ahmed Abdel Khalek
[J]. JOURNAL OF COMPUTER ASSISTED TOMOGRAPHY, 2019, 43 (05) : 786 - 792
[2] An atypical case of Klippel-Trenaunay syndrome presenting with crossed-bilateral limb hypertrophy and postaxial polydactyly: a case report
Al-Najjar, Rawan M.
Fonseca, Rafael
[J]. BMC PEDIATRICS, 2019, 19 (1)
[3] Radiological Aspect of Klippel-Trenaunay Syndrome: A Case Series With Review of Literature
Alwalid, Osamah
Makamure, Joyman
Cheng, Qi-guang
Wu, Wen-jun
Yang, Chao
Samran, Elham
Han, Ping
Liang, Hui-min
[J]. CURRENT MEDICAL SCIENCE, 2018, 38 (05) : 925 - 931
[4] Periosteal new bone formation in Klippel-Trenaunay syndrome: a case report
Fang, Xiang
Zhang, Wenli
Yu, Zeping
Kuang, Fuguo
Huang, Bin
Duan, Hong
[J]. BMC PEDIATRICS, 2020, 20 (01)
[5] Klippel Trenaunay Syndrome
Harna, Bushu
Tomar, Shekhar
[J]. INDIAN JOURNAL OF PEDIATRICS, 2020, 87 (11) : 966 - 967
[6] Keepanasseril A, 2017, OBSTET MED, V10, P177, DOI 10.1177/1753495X17719181
[7] Klippel M., 1900, Arch Gen Med, V185, P641
[8] Multimodality imaging approach in a patient with Klippel-Trenaunay syndrome
Ochoco, Gerard Eastdon Truadio Dales
Enriquez, Clare Angeli Guinto
De Lara Urgel, Ryan Jason
Catibog, Jason S.
[J]. BMJ CASE REPORTS, 2019, 12 (08)
[9] Clinical course of pediatric large vascular anomalies located in the extremities
Oktay, Burcu Kilinc
Kacar, Ayse Gonca
Ozel, Simge Cinar
Ocak, Suheyla
Celkan, Tiraje
[J]. TURKISH ARCHIVES OF PEDIATRICS, 2021, 56 (03): : 213 - 218
[10] Klippel-Trenaunay Syndrome in a Boy With Concomitant Ipsilateral Overgrowth and Undergrowth
Ruggieri, Martino
Pavone, Vito
Polizzi, Agata
Falsaperla, Raffaele
Fichera, Marco
Pavone, Piero
[J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2014, 164 (05) : 1262 - 1267

← 1 2 →