Results 61 to 70 of about 4,504 (202)
Hepatic Dearterialization for Nonresectable Liver Tumors in Five Dogs and Two Cats
Journal of Veterinary Internal Medicine, Volume 39, Issue 2, March/April 2025.ABSTRACT Introduction Some massive or nodular liver tumors can make surgical resection dangerous. Transarterial embolization and chemoembolization recently have been evaluated in dogs and cats, but multinodular or diffuse tumors make selective embolization difficult, impractical, and may require multiple anesthetic events.
Michelle T. Nguyen +2 more
wiley +1 more source
Case Reports in Endocrinology, 2015 Aim. Fibrous dysplasia is a rare bone disease caused by missense mutation leading to abnormal fibroblast and osteoblast proliferation and increased bone resorption. FD can present in monostotic or polyostotic forms. About 3% of FD could be in association
Nilufer Ozdemir Kutbay +4 more
doaj +1 more source
Paget's disease of bone: An entity still exists in India
Indian Journal of Endocrinology and Metabolism, 2018 Background: Paget's disease of bone (PDB) is uncommonly reported from India. We attempted to study the clinical and imaging features and management of participants who presented with PDB.
Kripa Elizabeth Cherian +9 more
doaj +1 more source
Legius syndrome: Case report and review of literature [PDF]
, 2015 A 8-month-old child was referred to our Dermatologic Unit for suspected Neurofibromatosis type 1 (NF 1), because of the appearance, since few days after birth, of numerous caf\ue9-au-lait spots (seven larger than 5 mm); no other sign evocative of NF 1 ...
Belcaro, Chiara +4 more
core +2 more sources
Veterinary Radiology &Ultrasound, Volume 66, Issue 1, January 2025.Abstract Laying hens are increasingly being kept in backyard flocks and considered family pets; however, diagnostic imaging characteristics of bone for clinically normal backyard hens are currently limited. This prospective, descriptive study was to describe radiographic, computed tomographic, and histologic characteristics of bone for a group of ...
Jeryl Jones +3 more
wiley +1 more source
Molecular effect of an OPTN common variant associated to Paget's disease of bone [PDF]
, 2018 Paget's disease of bone (PDB) is a chronic bone disorder and although genetic factors appear to play an important role in its pathogenesis, to date PDB causing mutations were identified only in the Sequestosome 1 (SQSTM1) gene at the PDB3 locus.
Brown, Jacques P. +5 more
core +3 more sources
Case Reports in Endocrinology, Volume 2025, Issue 1, 2025.Background: Fibrous dysplasia (FD) is a rare congenital bone disease. Denosumab, a monoclonal antibody targeting nuclear factor kappa‐B ligand (RANKL), suppresses osteoclast activity and exhibits therapeutic potential for FD. Case Presentation: We present the case of an adult female patient diagnosed with FD who had undergone 7 treatment cycles of ...
Danni Liu +5 more
wiley +1 more source
A rare case of solitary toxic nodule in a 3yr old female child – a case report [PDF]
, 2013 A three year old hyperactive female child presented with a midline neck swelling of one year duration. Clinical examination revealed a nodule in the isthmus of thyroid.Her Thyroid Stimulating Hormone (TSH) was suppressed and Free T3 and Free T4 levels ...
Karunakaran, Poongkodi +1 more
core +1 more source
Nasu-Hakola disease (PLOSL) : report of five cases and review of the literature [PDF]
, 2006 The combination of bilateral lytic lesions in the bones of the lower and upper extremities and presenile dementia is characteristic of polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy, also known as Nasu-Hakola disease.
Freyschmidt, Jürgen +3 more
core +2 more sources
Case Reports in Radiology, Volume 2025, Issue 1, 2025.Background Cherubism is a rare genetic disorder characterised by multilocular cystic lesions in the mandible and/or maxilla, which result in the typical cherub‐like face. Two forms of cherubism exist—hereditary (familial) and nonhereditary (nonfamilial)—and it usually occurs amongst children aged 2–7 years.
Seth Kwadjo Angmorterh +11 more
wiley +1 more source