نتایج جستجو برای: diffuse variant

تعداد نتایج: 162141  

2014
Yusuf Ziya Tan Sabire Yılmaz Meftune Özhan Metin Halaç

Thirty-six year old male patient with pathological fracture of the left tibia underwent intramedullary and soft tissue curettage. The histopathological examination revealed diffuse large B cell lymphoma. The patient underwent F18-FDG PET-CT scanning for initial staging. FDG PET-CT scan revealed hypermetabolic lesions at the left tibia and in bilateral kidneys. After the systemic chemotherapy an...

Journal: :SN Comprehensive Clinical Medicine 2023

Abstract Leigh syndrome (LS) or subacute necrotizing encephalomyelopathy is a progressive, lethal, mitochondrial disease mostly presenting in childhood. We report 36-year-old African male to the Emergency Department with 6-month history of progressive dysarthria. Examination also showed oculomotor limitations for downgaze and convergence, mild right hemiparesis Babinski sign, absent lower limb ...

Journal: :Journal of neurology, neurosurgery, and psychiatry 2005
M Mihara S Sugase K Konaka F Sugai T Sato Y Yamamoto S Hirota K Sakai S Sakoda

This paper reports a 59 year old woman with paraneoplastic limbic encephalitis associated with diffuse large B cell lymphoma. Her brain magnetic resonance imaging scan showed bilateral posterior thalamic hyperintensities, similar to the "pulvinar sign". Her symptoms included progressive psychiatric disturbance and resembled the initial symptoms of variant Creutzfeldt-Jakob disease (vCJD). Clini...

Journal: :The Journal of the Association of Physicians of India 2004
Sharon G Childs

Diffuse idiopathic skeletal hyperostosis (DISH) or Forestier's disease is characterized by calcification and ossification of soft tissue entheses of ligaments and tendons. DISH is believed to be a variant of osteoarthritis (OA) without the degenerative intervertebral disc and joint degenerative qualities seen in classic OA. The likely pathoetiologic causes of DISH are presented.

2016
Jeremy D.K. Parker Yaoqing Shen Erin Pleasance Yvonne Li Jacqueline E. Schein Yongjun Zhao Richard Moore Joanna Wegrzyn-Woltosz Kerry J. Savage Andrew P. Weng Randy D. Gascoyne Steven Jones Marco Marra Janessa Laskin Aly Karsan

In an attempt to assess potential treatment options, whole-genome and transcriptome sequencing were performed on a patient with an unclassifiable small lymphoproliferative disorder. Variants from genome sequencing were prioritized using a combination of comparative variant distributions in a spectrum of lymphomas, and meta-analyses of gene expression profiling. In this patient, the molecular va...

Journal: :Seizure 2001
Lütfü Hanoglu Nalan Kayrak Ertaş Ahmet Altunhalka Dursun Kirbaş

We describe a case with symptoms of transient diffuse right hemisphere dysfunction (hemispatial neglect, dyscalculia, and disturbance of both spatial construction and visuospatial perception) occurring after status epilepticus. The clinical picture of this case suggested to us that these features could be understood as a variant of Todd's paralysis.

Journal: :The Journal of the Association of Physicians of India 2007
N Anup D Dalus M K Suresh N Nileena

Pyrexia of unknown origin has always been a challenging problem to diagnose for physicians. Here we present a case of a splenic tumor, which after histopathology and immunohistochemistry, two possibilities were considered, a diffuse large cell lymphoma--plasmablastic variant and second an anaplastic plasmacytoma. The patient was treated with chemotherapy and on followup he has no evidence of re...

2015
Archana Shivamurthy Roumina Hasan Sushmitha Malpe Gopal Shaila Talengala Bhat Tanvi Shetty

Adenomyomatosis of the gallbladder is a benign and degenerative condition of the gallbladder. It is an incidental finding in gall bladder specimens resected for chronic cholecystitis or cholelithiasis. It frequently occurs after 3rd or 4th decade of life and is often an incidental finding in cholecystectomy specimens resected for chronic cholecystitis or cholelithiasis. Patients with adenomyoma...

Journal: :Annals of the rheumatic diseases 1989
P S Klimiuk A Grennan C Weinkove M I Jayson

Platelet serotonin concentrations were measured in 43 patients with systemic sclerosis, in 11 patients with primary Raynaud's phenomenon, and in 38 normal controls. Patients with the CREST variant (calcinosis, Raynaud's phenomenon, oesophageal dysmotility, sclerodactyly, telangiectasia) had significantly lower platelet serotonin concentrations than normal controls. Patients with diffuse systemi...

Journal: :Annals of the rheumatic diseases 1995
R La Corte G Bajocchi A Potena M Govoni F Trotta

OBJECTIVE To determine the frequency and relative risk of bronchial hyperreactivity to methacholine in systemic sclerosis patients with or without associated Sjögren's syndrome. METHODS A prospective study of 56 patients with systemic sclerosis (42 with the diffuse and 14 with the limited variant; 24 with associated Sjögren's syndrome), 57 with primary Sjögren's syndrome, and 61 healthy contr...

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