Hemolymphatic Malformation: Mixed Form Congenital Vascular Malformation

2017 ◽  
pp. 97-103
Author(s):  
James Laredo ◽  
Byung-Boong Lee
Keyword(s):  
Vascular Malformation ◽  
Mixed Form ◽  
Congenital Vascular Malformation

scholarly journals Congenital vascular malformation associated with multiple cranial, vertebral and upper limb skeletal abnormalities

2010 ◽  
Vol 92 (5) ◽  
pp. e18-e20 ◽  
Author(s):  
N Marsden ◽  
K Shokrollahi ◽  
K Maw ◽  
A Sierakowski ◽  
FA Bhat ◽  
...  
Keyword(s):  
Upper Limb ◽  
Vascular Malformation ◽  
Bone Growth ◽  
Vascular Malformations ◽  
Skeletal Abnormalities ◽  
Congenital Vascular Malformation ◽  
Individual Traits

The association between congenital vascular malformations and altered bone growth, the so-called vascular bone syndrome, is well documented. Various eponymous syndromes each with their individual traits, such as Klippel–Trenaunay, Parkes–Weber and Servelle–Martorell syndrome have been described, along with variations. We report on a previously undescribed case of congenital vascular malformation associated with multiple skeletal abnormalities affecting the skull, vertebrae and right upper limb, and discuss the literature.

scholarly journals Two Cases of Anomalous Origin of Left Coronary Artery From The Pulmonary Artery

2021 ◽  
Author(s):  
Zhao Juan ◽  
Zou Chunbo
Keyword(s):  
Coronary Artery ◽  
Pulmonary Artery ◽  
Vascular Malformation ◽  
Left Coronary Artery ◽  
Clinical Symptoms ◽  
Treatment Strategies ◽  
Anomalous Origin ◽  
Coronary Cta ◽  
Congenital Vascular Malformation

Abstract Coronary artery originating from pulmonary artery is a rare congenital vascular malformation, which generally presents corresponding clinical symptoms with the growth of patients' age. Coronary CTA and angiography are important methods for diagnosis of this disease, and provide evidence for treatment strategies of patients.

scholarly journals Multimodality imaging and interventional management of a complex congenital vascular malformation

2010 ◽  
Vol 14 (2) ◽  
pp. 32
Author(s):  
Aadil Ahmed
Keyword(s):  
Arteriovenous Malformation ◽  
Vascular Malformation ◽  
Clinical Presentation ◽  
Multimodality Imaging ◽  
Vascular Lesions ◽  
Liver Tumours ◽  
Congenital Vascular Malformation ◽  
Interventional Management ◽  
Benign Liver

Hepatic vascular lesions are not an uncommon finding in children, and represent the most common benign liver tumours to present in infancy. We present a case of a complex vascular malformation with an intrahepatic component suggestive of a venous/arteriovenous malformation as well as a large extrahepatic lesion. The extrahepatic mass was present in both sub- and supra-diaphragmatic locations ,with features of a congenital haemangioma. In view of the clinical presentation and different imaging appearances, this case was felt to be interesting in its radiological workup, management and eventual unusual pathology.

Prosthetic fitting in a patient with a transtibial amputation due to a congenital vascular malformation of the right leg

2013 ◽  
Vol 38 (2) ◽  
pp. 167-170 ◽  
Author(s):  
Elisabeth K Simmelink ◽  
Gerardus M Rommers ◽  
Jean W M Gardeniers ◽  
Henk Zijlstra
Keyword(s):  
Vascular Malformation ◽  
Weight Bearing ◽  
Ischial Tuberosity ◽  
Full Weight Bearing ◽  
Recurrent Bleeding ◽  
Transtibial Amputation ◽  
Congenital Vascular Malformation ◽  
The Right ◽  
High Level ◽  
Fitting In

Background: The problems of prescribing a prosthesis for a young girl with severe congenital vascular malformation deformity leading to a transtibial amputation. Case description and methods: Due to the high risk of recurrent bleeding and limitations regarding full weight bearing of the stump, a normal socket fitting process was not possible. Using a multidisciplinary approach, a prosthesis was designed to enable full weight bearing in a flexed knee position with ischial tuberosity support to prevent full weight bearing on the tibial part of the stump. Findings and outcomes: After training and adjustments to the design, a definitive prosthesis with a free motion mechanical knee joint could be used. During the training with this prosthesis, no skin problems were observed, and at the end of the rehabilitation, the patient had a high level of activities of daily living and sports. Conclusion: The above prosthetic solution with an adjusted socket design proved to be successful in this case. Clinical relevance In a patient with severe congenital vascular malformation deformity leading to a transtibial amputation, fitting of a good prosthesis without full weight bearing of the stump proved to be successful.

scholarly journals Early diagnosis of congenital vascular malformation as a condition to rapid prevention of complications – case study

2017 ◽  
Vol 13 (2) ◽  
pp. 260-266
Author(s):  
Dominika Jaguś ◽  
◽  
Agata Rutkowska ◽  
Paweł Wareluk ◽  
◽  
...  
Keyword(s):  
Early Diagnosis ◽  
Vascular Malformation ◽  
Congenital Vascular Malformation

Multiple Cutaneous Hemangiomas and Coarctation of the Aorta With Right Aortic Arch

PEDIATRICS ◽  
1988 ◽  
Vol 81 (5) ◽  
pp. 707-710
Author(s):  
LOÏC VAILLANT ◽  
GÉRARD LORETTE ◽  
ALAIN CHANTEPIE ◽  
MICHEL MARCHAND ◽  
DANIEL ALISON ◽  
...  
Keyword(s):  
Aortic Arch ◽  
Vascular Malformation ◽  
Congenital Anomalies ◽  
Coarctation Of The Aorta ◽  
Right Aortic Arch ◽  
Congenital Vascular Malformation

Strawberry hemangiomas are the most common congenital vascular malformation seen in infants. Usually, they appear as a raised bright or purplish red lobulated tumor with well-defined borders and capillaries protruding from its surface. They are not present at birth. They develop during the first weeks of life, grow rapidly during the first 6 months, remain stationary for awhile, and then undergo complete or partial involution and resolution without treatment. Usually, these hemangiomas are solitary or in small number1 and are not associated with congenital anomalies. We report a case of strawberry hemangiomas that is unusual because of the multiplicity and extension associated with laryngeal hemangioma and coarctation with right aortic arch.

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