Results 31 to 40 of about 64,001 (226)

Cavernous venous malformation (cavernous hemangioma) of the orbit: Current concepts and a review of the literature

open access: yes, 2017
The cavernous venous malformation of the orbit, previously called cavernous hemangioma, is the most common primary orbital lesion of adults. Cavernous venous malformation occurs more often in women and typically presents in the fourth and fifth decades ...
Grimaldi, Gabriela   +13 more
core   +2 more sources

Multiple cerebral cavernous malformations in a pediatric patient with Turner syndrome

open access: yesInterdisciplinary Neurosurgery, 2017
Turner syndrome (TS; 45,X0) is a relatively common chromosomal disorder that is associated with characteristic phenotypic stigmata: short stature, webbed neck, broad (“shield”) chest with widely spaced nipples, cubitus valgus, ovarian dysgenesis (“streak
Nicholas T. Gamboa, B.S.   +4 more
doaj   +1 more source

Venous malformation of the lung in an infant

open access: yesJournal of Pediatric Surgery Case Reports, 2019
Venous malformation of the lung is an extremely rare condition, and it is even rarer in infants. We present a case of cavernous hemangioma classified as venous malformation of the lung in an infant, which was initially diagnosed and treated as pneumonia.
Katsuhiro Ogawa   +2 more
doaj   +1 more source

Cavernous malformation hemorrhage due to trans-mural pressure alterations after cerebrospinal fluid diversion: a case report

open access: yesBMC Neurology, 2020
Background Cavernous malformations are rare cerebral pseudo-vascular lesions with annualized bleeding rates of 0.5–3% in most studies. Of the various explored risk factors for bleeding to date, only prior hemorrhage has shown significant correlation ...
Benjamin R. Hartley   +2 more
doaj   +1 more source

Surgical Treatment of Cavernous Angiomas in the Pineal Gland – Case Report

open access: yesBrazilian Neurosurgery, 2015
Pineal cavernous angioma is a vascular malformation that has a prevalence lower than 1%. The etiology is debated. It is believed that it is originated from an autosomal dominant inheritance or from radiotherapeutic treatment.
Joseph Franklin Chenisz   +4 more
doaj   +1 more source

A Rare Form of Microcephalic Primordial Dwarfism due to NSMCE2 Deficiency (Seckel Syndrome Type 10): A Report of Macular Involvement

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Biallelic variants in NSMCE2 (MMS21), which encodes the SUMO E3 ligase subunit of the SMC5/6 chromatin‐maintenance complex, have recently been implicated in microcephalic primordial dwarfism (MPD), corresponding to Seckel syndrome type 10 (OMIM #617246).
Cristina Peduto   +5 more
wiley   +1 more source

Subdural Hematoma From a Cavernous Malformation

open access: yes, 2014
Objective: To present a case of a cavernous malformation presenting with a subdural hematoma. Methods: A 27-year-old woman was admitted with progressively worsening headache, vomiting, weakness, and word-finding difficulties 1 week after she was ...
Schmitt, Anne J.   +4 more
core   +1 more source

Human evolution and the obstetrical dilemma: The pelvic floor hypothesis

open access: yesThe Anatomical Record, EarlyView.
Abstract Human childbirth is mechanically difficult because a large‐headed, broad‐shouldered fetus must pass through a comparatively narrow, twisted bony birth canal. Traditional explanations of this “obstetrical dilemma” emphasize the role of bipedal locomotion in inhibiting the evolution of a wider, more spacious pelvis.
Barbara Fischer, Ekaterina Stansfield
wiley   +1 more source

Intracranial meningioma and concomitant cavernous malformation: a series description and review of the literature

open access: yes, 2020
Objectives: Intracranial meningioma with concomitant cavernous malformation has been rarely described in the literature. This study aimed to investigate the correct neurosurgical conduct.
Sergio Paolini   +7 more
core   +1 more source

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