Results 1 to 10 of about 70,702 (248)

Vascular Anomalies

open access: yesClinics in Perinatology, 2018
Classified by their most prominent vessel type, congenital vascular tumors and malformations are frequently evident neonatally. Although many are identified in the first month of life, management is often delayed due to their slow expansion. Urgent interventions may be necessary in fast-growing, obstructive, destructive, or bleeding anomalies ...
Adam B, Johnson, Gresham T, Richter
  +9 more sources

Analysis of 18 complex diffuse arteriovenous malformation cases treated with percutaneous radiofrequency ablation

open access: yesBMC Cardiovascular Disorders, 2021
Background The aim of the present study is to evaluate the short-term efficacy and feasibility of radiofrequency ablation in the treatment of complex diffuse arteriovenous (AV) malformations.
Chun-Xiao Ge   +5 more
doaj   +1 more source

Gastrointestinal involvement in Klippel-Trénaunay syndrome: pathophysiology, evaluation, and management

open access: yesOrphanet Journal of Rare Diseases, 2023
Klippel-Trénaunay syndrome is typically a complex combined capillary-lymphatic-venous malformation in lower limb. Gastrointestinal involvement is not infrequent in Klippel-Trénaunay syndrome. Rectal bleeding is the most common complication.
Huaijie Wang   +5 more
doaj   +1 more source

Fibro-adipose vascular anomaly (FAVA) - diagnosis, staging and management

open access: yesOrphanet Journal of Rare Diseases, 2023
Background The diagnosis and treatment of fibro-adipose vascular anomaly (FAVA) of the limb remains challenging since this entity is rare and complex.
Huaijie Wang   +5 more
doaj   +1 more source

Myriocin enhances the antifungal activity of fluconazole by blocking the membrane localization of the efflux pump Cdr1

open access: yesFrontiers in Pharmacology, 2022
Introduction: Extrusion of azoles from the cell, mediated by an efflux pump Cdr1, is one of the most frequently used strategies for developing azole resistance in pathogenic fungi. The efflux pump Cdr1 is predominantly localized in lipid rafts within the
Hongkang Wang   +7 more
doaj   +1 more source

Case report: Experience of a rare case of rebound of the Kasabach-Merritt phenomenon during sirolimus treatment in kaposiform hemangioendothelioma

open access: yesFrontiers in Pediatrics, 2022
Kaposiform hemangioendothelioma (KHE) is a rare vascular neoplasm associated with the Kasabach–Merritt phenomenon (KMP), which is a consumptive coagulopathy with associated potentially life-threatening thrombocytopenia.
Liang Wang   +9 more
doaj   +1 more source

Vascular Anomalies

open access: yesDermatologic Clinics, 2022
Vascular anomalies are complex diseases with different clinical presentations. In ancient times, some purplish spots were already seen as a curse, and over the centuries, they began to be described as part of other diseases, gaining different eponyms.
Laura Andrews   +3 more
  +7 more sources

The efficacy of bleomycin sclerotherapy in the treatment of lymphatic malformations: a review and meta-analysis

open access: yesBrazilian Journal of Otorhinolaryngology, 2023
Objective: At present, bleomycin has been widely used in the treatment of Lymphatic Malformations (LMs). This study aims to perform a meta-analysis to investigate the effectiveness and influencing factors of bleomycin in the treatment of LMs. Methods: We
Jiali Sun   +4 more
doaj   +1 more source

Efficacy of OK-432 sclerotherapy for different types of lymphangiomas: a review and meta-analysis

open access: yesBrazilian Journal of Otorhinolaryngology, 2023
Objective: This study aims to perform a meta-analysis to figure out the efficacy of OK-432 sclerotherapy between Macrocystic (MAC) lymphangiomas and Microcystic (MIC) lymphangiomas.
Jiali Sun   +4 more
doaj   +1 more source

Complex vascular anomalies and tissue overgrowth of limbs associated with increased skin temperature and peripheral venous dilatation: parks weber syndrome or PROS?

open access: yesHereditas, 2022
PIK3CA-related overgrowth spectrum (PROS) is a series of congenital, sporadic disorders that are associated with segmental overgrowth phenotypes and postzygotic, somatic gene mutations in the PIK3CA-ATK-mTOR pathway.
Li Xin Su   +8 more
doaj   +1 more source

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