This study evaluated the histopathological lesions of the Chilean flounder, Paralichthys adspersus, inhabiting the marine coastal area influenced by the Itata River (central Chile) in order to provide an environmental baseline given the plans to discharge effluents from a cellulose plant through a submarine pipe in the area. Flounder were also sampled at two reference sites over the course of 1 year. Pathological examinations and descriptions of histopathological lesions follow the ICES suggested protocol: internal and histopathological lesions, condition factor, and hepatosomatic and spleen indexes. The prevalence of fish with histopathological lesions differed significantly among sites. The flounder sampled in the Itata area were the most affected. Evaluation of histopathological lesions observed on the flounder caught in the Itata area revealed (i) 16 different types of histopathological lesions, (ii) a high prevalence of lesions in gills and epidermal and hepatic tissue, and (iii) a normal K factor and hepatosomatic index. Significant differences were found in epidermal hyperplasia (EH), chronic dermatitis, telangiectasis (TEL), localized edema in the base of lamellae (LE), fusion of secondary lamellae (FSL), foci of cellular alteration (FCA), melanomacrophagic centers (MMCs), and hemosiderin (HEM) lesions among sites and among sites by season of the year. Winter 2006 was the most affected. A seasonal analysis of histopathological lesions on flounder caught in the Itata area showed significant differences for EH, progressive focal invasion of muscle fibers (PFIMF), TEL, LE, FSL, lamellar bifurcation, hepatitis, FCA, MMCs, and HEM lesions between the sampled seasons of the year; flounder caught in winter 2006 had the highest prevalence of these lesions except for PFIMF, which was higher in winter 2007. These results are discussed in relation to the contents of inorganic and organic compounds in the water column and the contents of organic compounds in sediments of the subtidal environment in the Itata area.
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http://dx.doi.org/10.1007/s00244-008-9223-5 | DOI Listing |
Background: Alport syndrome (AS) is a multifaceted condition that primarily affects the basement membranes of the kidneys, ears, and eyes. AS is considered the second most common cause of hereditary renal failure, exhibiting varied clinical manifestations across different lifespans. The aim of this study is to investigate the clinical features and genetic profile of AS and to elucidate the genotype-phenotype correlation of AS.
View Article and Find Full Text PDFBJU Int
January 2025
Division of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
Objective: To perform a systematic review and meta-analysis to assess the relationship between intraprostatic maximum standardised uptake value (SUV) of the dominant prostatic lesion as measured on preoperative prostate-specific membrane antigen (PSMA) positron emission tomography (PET) with radical prostatectomy International Society of Urological Pathology (ISUP) Grade Group, pathological tumour (pT) staging, and biochemical recurrence (BCR).
Methods: Prostate-specific membrane antigen PET may offer non-invasive assessment of histopathological and oncological outcomes before definitive treatment. SUV of the dominant lesion has been explored as a prognostic biomarker.
Equine Vet J
January 2025
Setor de Patologia Veterinária, Universidade Federal Do Rio Grande Do Sul, Porto Alegre, RS, Brazil.
Background: In horses, systemic calcinosis is a rare syndrome characterised by muscle lesion associated with the mineralisation of large muscle groups or other organs, in the absence of an alternative cause for the calcification, such as toxic, enzootic or metabolic. Molecular and histopathological aspects of the disease are still poorly elucidated.
Objectives: To describe the epidemiological, pathological and molecular aspects of systemic calcinosis in a convenience sample of six horses submitted to necropsy in the Southern and Midwestern regions of Brazil.
Childs Nerv Syst
January 2025
Department of Neuropathology, All India Institute of Medical Sciences, New Delhi, 110029, India.
Cerebral hydatid disease, caused by Echinococcus granulosus, is uncommon in children but presents significant diagnostic challenges due to its potential to mimic malignancy. Only a handful of cases with such a dilemma have been reported yet in the literature. We report a case of a 12-year-old female presenting with progressive headache and seizures, initially suspected to be a pilocytic astrocytoma.
View Article and Find Full Text PDFZhonghua Bing Li Xue Za Zhi
January 2025
Department of Pathology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou450052, China.
To investigate the clinicopathological and molecular genetic characteristics of intracranial mesenchymal tumors with FET::CREB fusion transcript. The clinical and imaging data of 6 cases of intracranial mesenchymal tumors with FET::CREB fusion from December 2018 to December 2023 were collected at the First Affiliated Hospital of Zhengzhou University. Their histological features, immunophenotype and molecular characteristics were analyzed.
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