Lower lip capillary malformation associated with lymphatic malformation without overgrowth: Part of the spectrum of CLAPO syndrome

2018 ◽  
Vol 35 (4) ◽  
pp. e243-e244 ◽  
Author(s):  
Camila Downey ◽  
Juan Carlos López-Gutiérrez ◽  
Esther Roé-Crespo ◽  
Luis Puig ◽  
Eulalia Baselga
Keyword(s):  
Lymphatic Malformation ◽  
Lower Lip ◽  
Capillary Malformation

Lower lip capillary malformation with sawtooth border in CLAPO syndrome

2021 ◽  
Author(s):  
Juan Jimenez‐Cauhe ◽  
Diogo Cerejeira ◽  
Diego Fernandez‐Nieto ◽  
Daniel Ortega‐Quijano ◽  
Pablo Boixeda
Keyword(s):  
Lower Lip ◽  
Capillary Malformation

Parkes Weber syndrome—Diagnostic and management paradigms: A systematic review

2016 ◽  
Vol 32 (6) ◽  
pp. 371-383 ◽  
Author(s):  
Igor Banzic ◽  
Milos Brankovic ◽  
Živan Maksimović ◽  
Lazar Davidović ◽  
Miroslav Marković ◽  
...  
Keyword(s):  
Systematic Review ◽  
Arteriovenous Malformation ◽  
Clinical Improvement ◽  
Venous Malformation ◽  
Lymphatic Malformation ◽  
Treatment Modalities ◽  
Eligibility Criteria ◽  
Capillary Malformation ◽  
Weber Syndrome ◽  
Klippel Trenaunay Syndrome

Objectives Parkes Weber syndrome is a congenital vascular malformation which consists of capillary malformation, venous malformation, lymphatic malformation, and arteriovenous malformation. Although Parkes Weber syndrome is a clinically distinctive entity with serious complications, it is still frequently misdiagnosed as Klippel–Trenaunay syndrome that consists of the triad capillary malformation, venous malformation, and lymphatic malformation. Methods We performed a systematic review investigating clinical, diagnostic, and treatment modalities of Parkes Weber syndrome (PubMed/MEDLINE, Embase, and Cochrane databases). Thirty-six publications (48 patients) fulfilled the eligibility criteria. Results The median age of patients was 23 years (IQR, 8–32), and 24 (50.0%) were males. Lower extremity was affected in 42 (87.5%) and upper extremity in 6 (12.5%) patients; 15 (31.3%) patients developed high-output heart failure; 12 (25.0%) patients had chronic venous ulcerations, whereas 4 (8.3%) manifested distal arterial ischemia. The spinal arteriovenous malformations were reported in six (12.5%) patients and coexistence of aneurysmatic disease in five (10.4%) patients. The most frequently utilized invasive treatments were embotherapy followed by amputation and surgical arteriovenous malformation resection, and occasionally stent-graft implantation. All modalities showed clinical improvement. However, long follow-up and outcome remained unclear. Conclusion A diagnosis of Parkes Weber syndrome should be made on the presence of capillary malformation, venous malformation, lymphatic malformation, and arteriovenous malformation (as main defect) in overgrowth extremity. Arteriovenous malformation presents the criterion for distinguishing Parkes Weber syndrome from Klippel-Trenaunay syndrome, which is substantial for treatment strategy. The primary management goal should be patient's quality of life improvement and complication reduction. Embolization alone/combined with surgical resection targeting occlusion or removal of arteriovenous malformation “nidus” reliably leads to clinical improvement.

An infant with a capillary malformation on the lower lip

2018 ◽  
Vol 35 (5) ◽  
pp. 681-682
Author(s):  
Hannelore De Maeseneer ◽  
Marta Ivars ◽  
Dirk Van Gysel
Keyword(s):  
Lower Lip ◽  
Capillary Malformation

Tumor of lower lip

1970 ◽  
Vol 101 (2) ◽  
pp. 241-244 ◽  
Author(s):  
L. M. Solomon
Keyword(s):  
Lower Lip

Reconstruction of Lower Lip with Innervated Serratus Anterior Muscle Flap

2014 ◽  
Vol 30 (S 01) ◽  
Author(s):  
A. Gundeslioglu ◽  
Dem Özen ◽  
Lorenc Jasharllari ◽  
Nebil Selimolu ◽  
Figen Güney ◽  
...  
Keyword(s):  
Muscle Flap ◽  
Serratus Anterior Muscle ◽  
Serratus Anterior ◽  
Lower Lip

A Case of Solitary Neurofibroma of the Lower Lip

2014 ◽  
Vol 57 (5) ◽  
pp. 333 ◽  
Author(s):  
So-Hee Choi ◽  
Do Hyun Kim ◽  
Bo-Young Kim
Keyword(s):  
Lower Lip ◽  
Solitary Neurofibroma
Sign in / Sign up

Export Citation Format

Share Document