Results 31 to 40 of about 410,183 (267)
Orphanet Journal of Rare Diseases, 2021 Background Lymphangioleiomyomatosis (LAM) is a rare multisystem disease characterized by cystic lung disease and extrapulmonary manifestations, including lymphatic system disorder.
Guozhu Hou +8 more
doaj +1 more source
Journal of Pediatric Surgery Case Reports, 2020 This case reports details a successful approach to the surgical management of an extensive penoscrotal microcystic lymphatic malformation in an adolescent male.
Aakanksha Desai +3 more
doaj +1 more source
Congenital cutaneous pedicled macrocystic lymphatic malformation on the upper extremity: A rare case report and review of the literature [PDF]
Archives of Aesthetic Plastic Surgery, 2019 Congenital cystic lymphatic malformations on the extremities are very rare. The patient described in this case study presented with a cutaneous and pedicled macrocystic lymphatic malformation that was eliminated by electrocauterization.
Chan Min Chung +3 more
doaj +1 more source
Lymphatic vascular morphogenesis in development, physiology, and disease [PDF]
, 2011 The lymphatic vasculature constitutes a highly specialized part of the vascular system that is essential for the maintenance of interstitial fluid balance, uptake of dietary fat, and immune response. Recently, there has been an increased awareness of the
Amélie Sabine +9 more
core +2 more sources
Axillary Web Syndrome Evidence for Lymphatic Origin with Thrombosis [PDF]
, 2020 Background: The axillary web syndrome (AWS) occurs in the axilla and on the frontal side of the upper arm and sometimes along the forearm to the thumb. The cord is painful, particularly on movement, and can therefore be very distressing for the patient ...
Johansson, Karin, +5 more
core +2 more sources
Prenatal Ultrasound Diagnosis of Klippel–Trenaunay Syndrome
Diagnostics, 2023 Klippel–Trenaunay syndrome (KTS) is a very rare vascular malformation syndrome also referred to as a capillary–lymphatic–venous malformation with unknown aetiology.
Nicolae Gică +6 more
doaj +1 more source
Are we nearly there yet? Coverage and compliance of mass drug administration for lymphatic filariasis elimination. [PDF]
, 2015 Lymphatic filariasis has been targeted for elimination by 2020, and a threshold of 65% coverage of mass drug administration (MDA) has been adopted by the Global Programme to Eliminate Lymphatic Filariasis (GPELF).
Alexander, Neal DE
core +1 more source
Case report: Noonan syndrome with protein-losing enteropathy
Frontiers in Genetics, 2023 Background: Noonan syndrome (NS) is characterized by typical facial features, short stature, congenital heart defects and other comorbidities. Lymphedema and chylous pleural effusions are also common in NS, but protein-losing enteropathy (PLE) is rarely ...
Yang Ou +6 more
doaj +1 more source
A Role for All-Trans-Retinoic Acid in the Early Steps of Lymphatic Vasculature Development [PDF]
, 2010 The molecular mechanisms that regulate the earliest steps of lymphatic vascular system development are unknown. To identify regulators of lymphatic competence and commitment, we used an in vitro vascular assay with mouse embryonic stem cell-derived ...
Dabouras, Vasilios +11 more
core +1 more source
Cervicofacial Lymphatic Malformations: A Retrospective Review of 40 Cases
Archives of Plastic Surgery, 2016 Background Lymphatic malformation (LM) is a form of congenital vascular malformation with a low incidence. Although LM has been studied, no consensus has emerged regarding its cause or treatment.
Byung Chae Cho +9 more
doaj +1 more source