Results 31 to 40 of about 8,801 (261)

MORPHOFUNCTIONAL FEATURES OF THE PLACENTA IN PREGNANT WOMEN WITH TUBERCULOSIS

open access: yesПаёми Сино, 2023
Objective: To study the morphology of the placenta in pregnant women with TB Methods: The morphology of the 26 placentas was evaluated in this study, out of which 15 were from women with various forms and localizations of TB (main group), while 11 ...
S.SH. VALDOSHOVA
doaj   +1 more source

Focal angiomatosis of the breast with MRI and histologic features

open access: yesRadiology Case Reports, 2017
Angiomatosis of the breast is an extremely rare, benign vascular lesion. This is a diagnostic challenge, given the limited number of cases reported in the literature.
Yasmin Mekhail, MD   +4 more
doaj   +1 more source

Bartonella species detection in captive, stranded and free-ranging cetaceans [PDF]

open access: yes, 2008
We present prevalence of Bartonella spp. for multiple cohorts of wild and captive cetaceans. One hundred and six cetaceans including 86 bottlenose dolphins (71 free-ranging, 14 captive in a facility with a dolphin experiencing debility of unknown origin,
Breitschwerdt, Edward B.   +15 more
core   +4 more sources

The Natural History of Retinal Vascular Changes from Infancy to Adulthood in Wyburn-Mason Syndrome

open access: yesMedicina, 2020
Wyburn-Mason syndrome is a rare, non-hereditary congenital neurocutaneous disorder leading to arteriovenous malformations. Malformations are characterized by an artery that is directly connected to veins without a capillary system and forms a fragile ...
Kristina Horkovicova   +4 more
doaj   +1 more source

Vanishing (Disappearing) Bone Disease in children: a review [PDF]

open access: yes, 2011
Vanishing bone disease is a very rare, peculiar destructive condition of the skeletal system resulting in spontaneous and progressive resorption and disappearance of osseous structures with replacement by vascular, fibrous connective tissue.
Nagaveni, N.B.   +3 more
core   +1 more source

Gorham Stout syndrome in a pediatric patient. A case report

open access: yesMedisur, 2023
Within the idiopathic osteolysis syndromes classification, Gorham-Stout disease ranks fourth. It is a clinical picture characterized by the progressive destruction of bone tissue and vascular proliferation, with angiomatosis and bone lymphangiomatosis ...
Ariel Moya Machado   +2 more
doaj  

Bacillary angiomatosis in a solid organ transplant recipient

open access: yesIDCases, 2019
We report a case of bacillary angiomatosis in a solid organ transplant recipient with typical skin lesions. Bacillary angiomatosis is an uncommon disease characterized by neovascular proliferation caused by infection with Bartonella henselae or ...
Jakob Ferløv Schwensen   +2 more
doaj   +1 more source

A Rare Case of Vascular Proliferation in the Mandible of a Juvenile Horse

open access: yesFrontiers in Veterinary Science, 2020
A fast growing, circumscribed, unilateral swelling of the right mandible of a juvenile horse was observed. Within few weeks, the continuously growing mass reached dimensions ranging from 7 to 10 cm in diameter and resulted in loss of the first deciduous ...
Eva Leitzen   +6 more
doaj   +1 more source

Ocular manifestations of Sturge–Weber syndrome: pathogenesis, diagnosis, and management [PDF]

open access: yes, 2016
Sturge-Weber syndrome has been included in the group of phakomatoses that is characterized by hamartomas involving the brain, skin, and eyes. The characteristic facial port-wine stain, involving the first branch of the trigeminal nerve and the embryonic ...
Abdolrahimzadeh, Solmaz   +4 more
core   +1 more source

Intracranial variant of encephalotrigeminal angiomatosis – A case report

open access: yesIndian Journal of Dental Research, 2019
Encephalotrigeminal Angiomatosis is a rare developmental phakomatoses characterized by the occurrence of nevus flammeus (port-wine stain) along the distribution of branches of trigeminal nerve, vascular angiomas in the eye, and leptomeningeal angiomas ...
N Mohan   +4 more
doaj   +1 more source

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