Publications by authors named "K Egervari"

Article Synopsis
  • Myxopapillary ependymomas (MPE) are rare, grade 2 spinal tumors known for their slow growth and benign nature but have a high recurrence risk and can spread through cerebrospinal fluid.* -
  • This study analyzed MRI characteristics and histopathological patterns in 13 patients with MPE, focusing on tumor location, size, signal intensity, and enhancement features.* -
  • Findings revealed typical MRI features such as T2 hyperintensity and contrast enhancement, with larger tumors often showing a microcystic pattern, while smaller tumors were usually solid, indicating a possible connection between tumor characteristics and histopathological patterns.*
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Ependymal and choroid plexus tumours arise in anatomically related regions. Their intraoperative differential diagnosis is large and depends on factors such as age, tumour site and clinical presentation. Squash cytology can provide valuable information in this context.

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Mutations affecting codon 172 of the isocitrate dehydrogenase 2 () gene define a subgroup of sinonasal undifferentiated carcinomas (SNUCs) with a relatively favorable prognosis and a globally hypermethylated phenotype. They are also recurrent (along with mutations) in gliomas, acute myeloid leukemia, and intrahepatic cholangiocarcinoma. Commonly reported mutations, all associated with aberrant IDH2 enzymatic activity, include R172K, R172S, R172T, R172G, and R172M.

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Immune-mediated necrotizing myopathy (IMNM) is a rare subtype of idiopathic inflammatory myopathy that is characterized by severe subacute proximal weakness, myofiber necrosis, and significantly elevated serum creatine kinase. Anti-signal recognition particle (SRP) and anti-3-hydroxy-3-methylglutaryl-coenzyme-A reductase autoantibodies have been found in about two-thirds of patients with IMNM. This myopathy is usually idiopathic and there is a scarce literature concerning its association with connective tissue diseases.

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