Results 41 to 50 of about 2,784,118 (172)

Venous Malformations in Childhood: Clinical, Histopathological and Genetics Update

open access: yesDermatopathology, 2021
Our knowledge in vascular anomalies has grown tremendously in the past decade with the identification of key molecular pathways and genetic mutations that drive the development of vascular tumors and vascular malformations.
Isabel Colmenero, Nicole Knöpfel
doaj   +1 more source

Blue rubber bleb nevus syndrome in a Malay girl: A case report and literature review. [PDF]

open access: yesInt J Surg Case Rep, 2020
INTRODUCTION: Blue Rubber Bleb Nevus Syndrome (BRBNS) also known as Bean’s Syndrome is an atypical type of vascular malformation. To date, around 200 cases have been reported world-wide. In view of its low incidence rate, clinicians might misdiagnose and
Mat Johar F   +4 more
europepmc   +3 more sources

Blue Rubber Bleb Nevus Syndrome - A Rare Cause of Anemia in Children [PDF]

open access: yesInternational Journal of Anatomy Radiology and Surgery, 2013
A 10 year old boy presented with generalized weakness and progressive pallor requiring multiple blood transfusions. The skin demonstrated multiple raised, bluish-black lesions over extremities, trunk and oral cavity.
Ashok V. Badakali   +2 more
doaj   +1 more source

Blue rubber bleb nevus syndrome

open access: yesOur Dermatology Online, 2022
We present an unusual case of a rare vascular disorder known as blue rubber bleb nevus syndrome (BRBNS). While many cases of BRBNS occur sporadically, some have been associated with an autosomal dominant inheritance pattern with a locus on chromosome 9p [1]. Furthermore, BRBNS causes vascular malformations to occur in the skin and the gastrointestinal (
Zachary Kolansky, Glenn Kolansky
openaire   +1 more source

Síndrome de Blue Rubber Bleb Nevus - relato de caso [PDF]

open access: yes
Introdução: A síndrome de Blue Rubber Bleb nevus (SBRBN) caracteriza-se por uma anomalia vascular que acomete a pele e vários órgãos como o trato gastrointestinal (TGI). As manifestações clínicas decorrem da perda crônica de sangue levando a um quadro de
Alves, Caroline Farias Marques
core   +1 more source

Blue rubber bleb nevus syndrome: Promising response to sirolimus

open access: yes, 2017
Blue rubber bleb nevus syndrome is a rare disease involving venous ...
AKYÜZ, CANAN   +2 more
core   +1 more source

Rare cause of recurrent iron deficiency anemia

open access: yesCHRISMED Journal of Health and Research, 2019
Blue rubber bleb nevus syndrome (BRBNS) is a rare disorder, characterized by multifocal venous malformations predominantly affecting skin, soft tissues, and gastrointestinal (GI) tract.
Rajesh Sharma   +4 more
doaj   +1 more source

A case of blue rubber bleb nevus syndrome

open access: yesThe Korean journal of internal medicine, 2008
Blue rubber bleb nevus syndrome is a rare disorder that is characterized by multiple recurrent vascular malformations, such as hemangioma, and these primarily involve the skin and the gastrointestinal tract. It may also involve the brain, liver, lungs, and skeletal muscles.
Shin, Seung-Hwan   +6 more
openaire   +2 more sources

A Novel Endoscopic Treatment for Blue Rubber Bleb Nevus Syndrome [PDF]

open access: yes, 2020
Introduction: Blue Rubber Bleb Nevus Syndrome (BRBNS), also known as Bean Syndrome, is a rare congenital disorder characterized by numerous, cutaneous and internal venous malformations, most commonly involving the skin and gastrointestinal tract (GI ...
Kakos, Diana   +3 more
core   +1 more source

Outcomes of Live Virus Vaccination in Patients With Vascular Anomalies Being Treated With Sirolimus

open access: yesPediatric Blood &Cancer, Volume 73, Issue 7, July 2026.
ABSTRACT Background Live vaccination in patients with vascular anomalies (VA) receiving sirolimus remains controversial due to immunosuppressive effects and theoretical risks. Procedure This single‐center retrospective study included patients with VA less than 4 years old at the start of sirolimus therapy who were incompletely vaccinated.
Svatava Merkle   +5 more
wiley   +1 more source

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