Zobrazeno 1 - 10
of 289
pro vyhledávání: '"Parkes Weber syndrome"'
Autor:
Hiroto Yasumura, MD, Koji Tao, MD, PhD, Ryo Imada, MD, Yushi Yamashita, MD, Naoki Tateishi, MD, Kenichi Arata, MD, PhD, Tamahiro Kinjo, MD, PhD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 11, Pp 4766-4774 (2024)
A 63-year-old woman presented with a giant arteriovenous malformation (AVM) of the lower limbs associated with Parkes Weber syndrome (PWS). The AVM was supplied by 4 branches of the right profunda femoris artery and 4-stage embolization was performed
Externí odkaz:
https://doaj.org/article/ffd1826dce444d00a1a0a273d607c0db
Publikováno v:
Indian Dermatology Online Journal, Vol 15, Iss 3, Pp 480-486 (2024)
International Society for the Study of Vascular Anomalies classification defines Congenital Limb Overgrowth Vascular Syndromes (CLOS) as a subset of vascular syndromes with other abnormalities that present with unilateral limb overgrowth. It includes
Externí odkaz:
https://doaj.org/article/feba746bfb254165bb3df4627c074d86
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Kazuya Tsukamoto, Hirotaka Koyanagi, Yusuke Nakagawa, Shingo Sato, Hideyuki Koga, Toshitaka Yoshii, Atsushi Okawa
Publikováno v:
Annals of Vascular Surgery - Brief Reports and Innovations, Vol 2, Iss 2, Pp 100094- (2022)
Background: Parkes-Weber syndrome is a rare congenital vascular abnormality involving aggressive overgrowth of vascular structures. Destruction of the surrounding bone, muscle, and joint tissues often occurs, resulting in pain while walking and reduc
Externí odkaz:
https://doaj.org/article/d3d8b13a88ac4092bd25db192540ef6e
Autor:
Ibrahim Al Kindi, Edwin Stephen, Ibrahim Abdelhady, Hanan Al-Mawaali, Rashid Al Sukaiti, Khalifa Al-Wahaibi
Publikováno v:
Indian Journal of Vascular and Endovascular Surgery, Vol 8, Iss 2, Pp 184-186 (2021)
We present three cases that were seen at our tertiary care hospital in Oman over the past 18 months. The paucity of knowledge of Parkes–Weber syndrome had these three patients visit several centers nationally and internationally. Through this case
Externí odkaz:
https://doaj.org/article/ea4d4290867242f1a3f0f406f84067c1
Autor:
Thilina Gunawardena, Manujaya Godakandage, Balasubramaniyam Saseekaran, Rezni Cassim, Mandika Wijeyaratne
Publikováno v:
Jornal Vascular Brasileiro, Vol 20 (2021)
Abstract Varicose veins of the lower limbs are common. However, pulsatile varicose veins are unusual. They could be an indicator of a sinister underlying pathology, such as severe cardiac dysfunction. It is easy to miss these rare cases during clinic
Externí odkaz:
https://doaj.org/article/2888af6d864d4f97aa4a47f51bfd9689
Publikováno v:
Journal of Education, Health and Sport, Vol 9, Iss 8, Pp 987-997 (2019)
Introduction: Parkes Weber Syndrome (PWS) is a traditional eponymous denomination of a certain type of angiodysplasia. It is a congenital vascular disease which consists of capillary malformation (CM), venous malformation (VM), lymphatic malformation
Externí odkaz:
https://doaj.org/article/fde21b10c022420ea64715d67241e67e
Autor:
Chris Tae Young Chung, Hyunmin Ko, Hyo Kee Kim, Hyejin Mo, Ahram Han, Sanghyun Ahn, Sangil Min, Seung-Kee Min
Publikováno v:
Vascular Specialist International, Vol 35, Iss 3, Pp 165-169 (2019)
A 58-year-old male patient with severe claudication due to thrombosis of the left ilio-femoro-popliteal artery aneurysm. He also had a venous stasis ulcer with a history of multiple embolotherapy of arteriovenous malformation. Duplex sonography revea
Externí odkaz:
https://doaj.org/article/e26f20e8f71a4a268dadf5b472852cfa
Autor:
Andrea Diociaiuti, Roberta Rotunno, Elisa Pisaneschi, Claudia Cesario, Claudia Carnevale, Angelo Giuseppe Condorelli, Massimo Rollo, Stefano Di Cecca, Concetta Quintarelli, Antonio Novelli, Giovanna Zambruno, May El Hachem
Publikováno v:
Biomedicines, Vol 10, Iss 6, p 1460 (2022)
Sporadic vascular malformations (VMs) are a large group of disorders of the blood and lymphatic vessels caused by somatic mutations in several genes—mainly regulating the RAS/MAPK/ERK and PI3K/AKT/mTOR pathways. We performed a cross-sectional study
Externí odkaz:
https://doaj.org/article/286a4664c31047ca98bd1ba1ccf12e52
Autor:
Josiah M. Peñalver, MD, James T. Bennett, M.D., Ph.D., Zoe Nelson, C.G.C., Randall A. Bly, M.D., Jonathan A. Perkins, D.O., Catherine V. Bull, A.R.N.P., Alberto Aliseda, Ph.D., Fanette Chassagne, Ph.D., Giridhar M. Shivaram, M.D., Antoinette W. Lindberg, M.D., John H.T. Waldhausen, M.D., Muhammad A.K. Nuri, M.B. B.S.
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 66, Iss , Pp 101780- (2021)
Parkes Weber syndrome is a fast-flow and slow-flow vascular anomaly with limb overgrowth that can lead to congestive heart failure and limb ischemia. Current management strategies have focused on symptom management with focal embolization. A pediatri
Externí odkaz:
https://doaj.org/article/a03b7713a84448ef98d16ab9ebb56a26