Zobrazeno 1 - 10
of 2 703
pro vyhledávání: '"Vascular anomaly"'
Autor:
Rathnaganpathi Thulasikumar, Mahesh Gogineni, Manoj Prabakar Ravichandran, Marun Raj Gnanasekaran
Publikováno v:
Indian Journal of Vascular and Endovascular Surgery, Vol 11, Iss 3, Pp 197-200 (2024)
Arteriovenous malformations (AVMs) are rare vascular abnormalities that can result from defects in blood vessels. They are not often found in the facial area, and this report describes a case of a high-flow AVM in an adult patient with swelling in th
Externí odkaz:
https://doaj.org/article/b34dfd8d2b6746cd99c24fd1b9b1f991
Autor:
Yazan M.S. Dibas, Mohammed Qasarwa
Publikováno v:
Radiology Case Reports, Vol 19, Iss 11, Pp 5485-5487 (2024)
Partial duplication of the left ovarian vein is an extremely rare anatomical variation with significant clinical implications. We report the case of a 52-year-old female with no significant medical history, presenting with a 2-month history of vague
Externí odkaz:
https://doaj.org/article/0fa9a16e291f4b91b273b49c3d52521b
Publikováno v:
Dermatology Reports (2024)
Unilateral Nevoid Telangiectasia (UNT) is a rare congenital or acquired benign cutaneous vascular anomaly, first identified by Blaschko in 1899. It is characterized by superficial telangiectasias with a reticular or linear pattern on one side of the
Externí odkaz:
https://doaj.org/article/44d92f61b2144262b5c8f5b1db7eca0d
Publikováno v:
Journal of Vascular Surgery Cases and Innovative Techniques, Vol 10, Iss 6, Pp 101597- (2024)
Torrential bleeding is a rare and life-threatening complication of arteriovenous malformations (AVMs). We report a case of head and neck AVMs present with uncontrollable torrential bleeding, which was treated with embolization and sclerotherapy. Then
Externí odkaz:
https://doaj.org/article/299af27b574446308f3b850e1c03277e
Autor:
Beatriz Ramos Santos Muniz, MD, Edwaldo Edner Joviliano, MD, PhD, Marcelo Bellini Dalio, MD, PhD, Eloisa Spinassé Giacomin, MD, Willams Germano Bezerra Segundo, MD, Karoline Evelyn Barbosa Gomes, MD
Publikováno v:
Journal of Vascular Surgery Cases and Innovative Techniques, Vol 10, Iss 4, Pp 101509- (2024)
A persistent sciatic artery (PSA) is a rare congenital vascular anomaly, with an estimated prevalence ranging from 0.01% to 0.05%. This condition can cause ischemic events in the lower limbs and sciatic artery aneurysms but can also be asymptomatic.
Externí odkaz:
https://doaj.org/article/8d2d4fb2ccaf4c7f9ca6b38accdf2792
Publikováno v:
Clinical Dermatology Review, Vol 8, Iss 2, Pp 107-112 (2024)
Background: Vascular anomalies are a group of disorders that are divided into two categories: tumors and malformations. Given the vast diversity of clinical presentations with overlapping signs and symptoms, diagnosis can be difficult. Objective: We
Externí odkaz:
https://doaj.org/article/f4336fe3a52b49df81e2cef0ceb3ff6a
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-9 (2024)
Abstract Background Vascular anomalies (VAs) are rare congenital disorders that can cause pain, disfigurement, coagulopathy, asymmetric growth, and disability. Patients with complex VAs experience multiple barriers to accessing expert care. It is imp
Externí odkaz:
https://doaj.org/article/7c83d253023e4cc291ec77cc44a59c50
Publikováno v:
Clinical Case Reports, Vol 12, Iss 3, Pp n/a-n/a (2024)
Key Clinical Message Patent foramen ovale (PFO) is the most common interatrial septal abnormality. The indications for PFO device closure are still being evaluated, with the most common reason being to prevent cerebrovascular accidents (CVA) caused b
Externí odkaz:
https://doaj.org/article/cae53026b14e4c3aa00c8c6463bbc420
Autor:
Madhuri Howdekar, Rammurti Susarla, Phani Chakravarty Mutnuru, Paramjyothi GK, Sanjeeva Prasad Kalva
Publikováno v:
Journal of Clinical Interventional Radiology ISVIR, Vol 07, Iss 03, Pp 215-217 (2023)
We report a case of a 34-year-old woman who presented with chest pain, shortness of breath, and dry cough of 1 month duration. Contrast-enhanced computed tomography of the chest revealed an enlarged and tortuous right pulmonary vein that could not co
Externí odkaz:
https://doaj.org/article/f72afa9a82774940bd6c5b7acc6e74e9
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-13 (2023)
Abstract Background The diagnosis and treatment of fibro-adipose vascular anomaly (FAVA) of the limb remains challenging since this entity is rare and complex. This paper is aimed to describe the clinical and imaging features, staging and management
Externí odkaz:
https://doaj.org/article/3dca27367d9e4cb7bcfa3ecdb7b3a8be