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1.
Clin Case Rep ; 10(3): e05530, 2022 Mar.
Article in English | MEDLINE | ID: mdl-35261775

ABSTRACT

An 83-year-old man was diagnosed with tuberculous pleuroperitonitis on a thoracoscopic pleural biopsy. It may be due to endogenous reactivation of the foci in the pleura and peritoneum. Thoracoscopy, which can be performed under local anesthesia, should be considered when both pleural effusion and ascites are present.

2.
Hum Mol Genet ; 26(6): 1173-1181, 2017 03 15.
Article in English | MEDLINE | ID: mdl-28158406

ABSTRACT

Although periventricular nodular heterotopia (PNH) is often found in the cerebral cortex of people with thanatophoric dysplasia (TD), the pathophysiology of PNH in TD is largely unknown. This is mainly because of difficulties in obtaining brain samples of TD patients and a lack of appropriate animal models for analyzing the pathophysiology of PNH in TD. Here we investigate the pathophysiological mechanisms of PNH in the cerebral cortex of TD by utilizing a ferret TD model which we recently developed. To make TD ferrets, we electroporated fibroblast growth factor 8 (FGF8) into the cerebral cortex of ferrets. Our immunohistochemical analyses showed that PNH nodules in the cerebral cortex of TD ferrets were mostly composed of cortical neurons, including upper layer neurons and GABAergic neurons. We also found disorganizations of radial glial fibers and of the ventricular lining in the TD ferret cortex, indicating that PNH may result from defects in radial migration of cortical neurons along radial glial fibers during development. Our findings provide novel mechanistic insights into the pathogenesis of PNH in TD.


Subject(s)
Cerebral Cortex/physiopathology , Fibroblast Growth Factor 8/metabolism , Periventricular Nodular Heterotopia/physiopathology , Thanatophoric Dysplasia/physiopathology , Animals , Cerebral Cortex/metabolism , Disease Models, Animal , Electroporation , Ependymoglial Cells/metabolism , Ferrets/genetics , Ferrets/physiology , Fibroblast Growth Factor 8/genetics , GABAergic Neurons/metabolism , Humans , Mice , Periventricular Nodular Heterotopia/etiology , Periventricular Nodular Heterotopia/genetics , Thanatophoric Dysplasia/complications , Thanatophoric Dysplasia/genetics
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