Results 71 to 80 of about 7,157 (217)

A rare case of a 5‐year‐old girl with Klippel–Trénaunay syndrome and a bleeding focal vulvar hemangioma in Uganda

open access: yesClinical Case Reports, Volume 12, Issue 10, October 2024.
Key Clinical Message Klippel–Trénaunay syndrome can present with atypical manifestations such as a bleeding vulvar hemangioma. This case report, the first documented in Uganda, highlights the need for awareness of such presentations and underscores the importance of continuous follow‐up in female patients to manage potential complications throughout ...
Mundeli Simon Peter   +2 more
wiley   +1 more source

Interventional Treatment of a Symptomatic Neonatal Hepatic Cavernous Hemangioma Using the Amplatzer Vascular Plug [PDF]

open access: yes, 2018
Percutaneous intervention is one treatment option for symptomatic hepatic hemangioma in infants. We report the case of a newborn (birth weight 4060 g) with a large hepatic cavernous hemangioma, which presented early with high cardiac output failure due ...
Bernet, Vera   +2 more
core  

Angioleiomyoma affecting the lips : report of 3 cases and review of the literature [PDF]

open access: yes, 2011
Angioleiomyoma is an uncommon benign soft tissue tumor usually found in the lower extremities and rarely observed in oral tissues. It is microscopically characterized as a proliferation of smooth muscle cells intermingled with abundant vascular channels.
Almeida, Oslei Paes de   +5 more
core   +1 more source

Cerebellar Dentate Cavernoma Enlargement and Tremor Emergence: Longitudinal Neuroimaging Analysis of Case Report and Literature Review

open access: yes
Movement Disorders Clinical Practice, Volume 12, Issue 9, Page 1410-1414, September 2025.
Andrew Z. Yang   +15 more
wiley   +1 more source

Multiple glomus tumours: Clinical, ultrasonographic and histopathologic findings of a rare disease

open access: yesSkin Health and Disease, Volume 4, Issue 5, October 2024.
Glomus tumour is a rare benign neoplasm originating from the glomus body, clinically presenting as a violet‐coloured, painful nodule more sensitive when exposed to cold or hot. This hamartoma is typically solitary and predominantly affects the limbs, extremities and nail beds. The appearance of multiple tumours and lesions not placed in the extremities
Bárbara Wiese   +4 more
wiley   +1 more source

Blue rubber-bleb nevus syndrome: report of a familial case with a dural arteriovenous fistula [PDF]

open access: yes, 2003
We report a case of a 45-year-old woman known to have a familial form of blue rubber-bleb nevus syndrome (BRBNS). The patient developed severe occipital headaches and bilateral retroauricular bruits.
Barbosa, V   +3 more
core  

Fatal giant pediatric intracranial cavernous angioma

open access: yesThe Turkish Journal of Pediatrics, 2006
Cavernous angioma is a benign vascular lesion that may occur in the central nervous system. The symptoms of raised intracranial pressure or consciousness alteration are usually related to acute hemorrhage.
Funda Corapçioğlu   +4 more
doaj  

Inherited cavernous malformations of the central nervous system: clinical and genetic features in 19 Swiss families [PDF]

open access: yes, 2018
Cavernous malformations (CCMs) are benign, well-circumscribed, and mulberry-like vascular malformations that may be found in the central nervous system in up to 0.5% of the population. Cavernous malformations can be sporadic or inherited.
Andermann, F.   +11 more
core  

Long-term safety and stability of angiogenesis induced by balanced single-vector co-expression of PDGF-BB and VEGF164 in skeletal muscle [PDF]

open access: yes, 2016
Therapeutic angiogenesis by growth factor delivery is an attractive treatment strategy for ischemic diseases, yet clinical efficacy has been elusive. The angiogenic master regulator VEGF-A can induce aberrant angiogenesis if expressed above a threshold ...
Banfi, Andrea   +7 more
core   +1 more source

Mutation prevalence of cerebral cavernous malformation genes in Spanish patients [PDF]

open access: yes, 2017
[Objective] To study the molecular genetic and clinical features of cerebral cavernous malformations (CCM) in a cohort of Spanish patients.[Methods] We analyzed the CCM1, CCM2, and CCM3 genes by MLPA and direct sequencing of exons and intronic boundaries
Delgado-Valverde, Mercedes   +9 more
core   +1 more source

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