keyword
https://read.qxmd.com/read/27411422/systemic-onset-juvenile-idiopathic-arthritis-with-macrophage-activation-syndrome-and-coronary-artery-dilatation-misdiagnosed-as-kawasaki-disease
#41
JOURNAL ARTICLE
Gonca Keskindemirci, Nuray Aktay Ayaz, Neslihan Melikoğlu, Helen Bornaun, Çiğdem Aydoğmuş, Esin Aldemir, Gönül Aydoğan
Systemic onset juvenile idiopathic arthritis (SoJIA) is characterized by arthritis, fever and visceral organ involvement including hepatosplenomegaly, lympadenopathy and serositis. This is a case of SoJIA misdiagnosed as Kawasaki disease (KD) and developed machrophage activation syndrome (MAS) secondary to Ebstein-Barr virus (EBV) infection. It is presented to point out the conditions that may come along. First of all, SoJIA should be kept in mind while making the differential diagnosis of coronary arterial ectasias and dilatations usually seen in vasculitic diseases like KD...
September 2015: Turkish Journal of Pediatrics
https://read.qxmd.com/read/26832181/natural-killer-like-t-cell-lymphoma-localized-to-the-terminal-ileum-case-report
#42
JOURNAL ARTICLE
Ümit Bayol, Süheyla Cumurcu, Kerem Karaman, Cem Tuğmen, Çağlar Akdeniz, Özlem Akman, Saime Ünlüoğlu
Intestinal intraepithelial lymphocytes are non-organized lymphoid populations that are composed of heterogeneous subsets with diverse ontogeny and phenotypes, and the differential diagnosis is crucial. A 43-year-old male patient underwent an emergency laparotomy due to a perforated mass of the terminal ileum. A right hemicolectomy plus small bowel resection was performed. Histopathological examination showed medium to large cells with vesicular nuclei, including marked nucleoli with large, colorless cytoplasm...
2016: Türk Patoloji Dergisi
https://read.qxmd.com/read/26709095/expression-of-serum-sialic-acid-early-antigen-iga-and-viral-capsid-antigen-iga-in-nasopharynx-cancer-patients-the-diagnostic-implication-of-combined-assays
#43
JOURNAL ARTICLE
Yuning Sun, Caibo Sun, Endong Zhang
BACKGROUND Ebstein-Barr virus (EBV) plays a critical role in nasopharynx cancer, which can be effectively monitored by serum levels of early antigen antibody (EA-IgA) and viral capsid antigen antibody (VCA-IgA). This study explored the diagnostic value of combined assays of sialic acid (SA), EA-IgA, and VCA-IgA via the expressional assay. MATERIAL AND METHODS A total of 42 nasopharynx cancer patients and 42 benign rhinitis and healthy controls were recruited in this study. Serum EA-IgA and VCA-IgA were tested by enzyme-linked immunosorbent assay (ELISA) and enzymatic assay of serum SA...
2015: Medical Science Monitor: International Medical Journal of Experimental and Clinical Research
https://read.qxmd.com/read/26191775/correlation-analysis-of-nasopharyngeal-carcinoma-tnm-staging-with-serum-ea-iga-and-vca-iga-in-ebv-and-vegf-c-and-d
#44
JOURNAL ARTICLE
Ruimei Sun, Xiaoli Wang, Xiaojiang Li
BACKGROUND: Nasopharyngeal carcinoma often occurs in humans in the nasopharyngeal epithelium area. Ebstein-Barr (EB) virus plays a key role in the process of nasopharyngeal carcinoma lesions. Early antigen antibody (EA-IgA) and viral capsid antigen IgA (VCA-IgA) of EB virus detection in serum can effectively monitor the process of nasopharyngeal carcinoma lesions. Serum vascular endothelial growth factor (VEGF) -C and VEGF-D expression detection can reflect the distant metastases ability of human tumor cells...
2015: Medical Science Monitor: International Medical Journal of Experimental and Clinical Research
https://read.qxmd.com/read/25896166/hiv-associated-lymphocytic-interstitial-pneumonia-a-clinical-histological-and-radiographic-study-from-an-hiv-endemic-resource-poor-setting
#45
JOURNAL ARTICLE
Richard N van Zyl-Smit, Jashira Naidoo, Helen Wainwright, Quanita Said-Hartley, Malika Davids, Hillel Goodman, Sean Rogers, Keertan Dheda
BACKGROUND: There is a paucity of clinical and histopathological data about HIV-associated lymphocytic interstitial pneumonitis (LIP) in adults from HIV endemic settings. The role of Ebstein-Barr virus (EBV) in the pathogenesis remains unclear. METHODS: We reviewed the clinical, radiographic and histopathological features of suspected adult LIP cases at the Groote Schuur Hospital, Cape Town South Africa, over a 6 year period. Archived tissue sections were stained for CD3, CD4, CD8, CD20 and LMP-1 antigen (an EBV marker)...
April 22, 2015: BMC Pulmonary Medicine
https://read.qxmd.com/read/25811010/vitamin-b12-and-vitamin-d-deficiencies-an-unusual-cause-of-fever-severe-hemolytic-anemia-and-thrombocytopenia
#46
Vikas A Mishra, Rishit Harbada, Akhilesh Sharma
The array of diagnostic workup for pyrexia of unknown origin (PUO) generally revolves in searching for infections, inflammatory/autoimmune, and endocrine etiologies. A differential diagnosis of fever, hemolytic anemia, and thrombocytopenia can have etiologies varying from infections like malaria, dengue, cytomegalovirus, Ebstein barr virus, Parvovirus, infective endocarditis, to autoimmune disorder (systemic lupus erythromatosis), vasculitis, hemolytic uremic syndrome, thrombotic thrombocytopenic purpura (TTP), autoimmune hemolytic anemia/Evan's syndrome, paroxysmal nocturnal hemoglobinuri (PNH), or drugs...
2015: Journal of Family Medicine and Primary Care
https://read.qxmd.com/read/25624957/central-nervous-system-lymphoma-in-a-3-year-old-male-suffering-from-a-severe-juvenile-xanthogranuloma-the-usefulness-of-perfusion-weighted-imaging-and-diffusion-weighted-imaging-in-the-diagnostics-of-pediatric-brain-tumors
#47
JOURNAL ARTICLE
Małgorzata Neska-Matuszewska, Anna Zimny, Krzysztof Kałwak, Marek J Sąsiadek
BACKGROUND: Primary Central Nervous System Lymphomas (PCNSLs) are rare, malignant brain tumors derived from lymphocytes B. Juvenile xanthogranuloma (JXG) is a non-Langerhans histiocytic cell disorder in children which mostly affects the skin. Rare fatalities have been reported in extracutaneous manifestation. Brain magnetic resonance imaging (MRI) is a method of choice in the diagnostics of all neoplastic CNS lesions. Perfusion weighted imaging (PWI) and diffusion weighted imaging (DWI) allow for more detailed analysis of brain tumors including the rate of neoangiogenesis and cellularity...
2015: Polish Journal of Radiology
https://read.qxmd.com/read/25610149/guillain-barr%C3%A3-syndrome-during-active-brucellosis
#48
Recep Aygul, Orhan Deniz, Metin Guzelcik, Dilcan Kotan
It has been reported that approximately two thirds of patients diagnosed with Guillain-Barré syndrome (GBS) have had a prodromal illness within a four-week period preceding the onset of GBS. This prodromal illness is most commonly an upper respiratory tract illness or, secondly, gastroenteritis. However, specific infectious agents, such as mycoplasma, cytomegalovirus, Ebstein-Barr virus, vaccinia, variola, campylobacter, varicella-zoster, measles, mumps, hepatitis A and B viruses, rubella, influenza A and B viruses, coxackie and echoviruses, have also been reported to be certain or probable etiologic antecedent agents of GBS...
December 2010: Eurasian Journal of Medicine
https://read.qxmd.com/read/25531150/angiocentric-and-intravascular-lymphomas
#49
REVIEW
D Tomasini, E Berti
Under the generic diagnosis of angiocentric and intravascular lymphomas are included several subtypes of lymphomas histopathologically characterized either by the predominantly endovascular-endoluminal presence of neoplastic lymphocytes of B-T or NK/T cell origin, or by a pathologic process centered around a blood vessels secondarily infiltrated and invaded by the spreading infiltrate. This group of lymphoproliferative disorders is heterogeneous regarding phenotype, but they share common features that are multiorgan involvement, worse prognosis, and, frequently Ebstein-Barr virus (EBV) genomic integration...
February 2015: Giornale Italiano di Dermatologia e Venereologia: Organo Ufficiale, Società Italiana di Dermatologia e Sifilografia
https://read.qxmd.com/read/25332588/hepatitis-a-virus-infection-associated-hemophagocytic-lymphohistiocytosis-in-two-children
#50
Kirubakaran Navamani, Manivachagan Muthappa Natarajan, Arul Premanand Lionel, Sathish Kumar
Hemophagocytic lymphohistiocytosis (HLH) is a syndrome characterized by high fever, maculopapular rash, neurological symptoms, abnormal liver functions and coagulopathy. Primary HLH is due to an underlying genetic abnormality. Secondary HLH are due to an underlying infection, autoimmune disease or malignancy. Secondary HLH due to viral infections are commonly due to the herpes group commonest of which is the Ebstein Barr virus (EBV). We describe two children with virus associated hemophagocytic lymphohistiocytosis (VAHLH) secondary to hepatitis A infection...
September 2014: Indian Journal of Hematology & Blood Transfusion
https://read.qxmd.com/read/25250166/hepatitis-c-infection-incidence-among-the-non-hodgkin-s-b-cell-lymphoma-patients-in-the-northeast-of-iran
#51
JOURNAL ARTICLE
Seyed Amir Aledavood, Mohammad Reza Ghavam-Nasiri, Kamran Ghaffarzadegan, Hamid Reza Raziee, Golnaz Saboori, Kazem Anvari, Samira Mohtashami, Mitra Ahadi, Bahram Memar
BACKGROUND: Various infectious agents like Ebstein Barr Virus (EBV), HTLV-1 and Helicobacter pylori have known as etiologic factors in different sub-types of lymphoma. Although Hepatitis C virus (HCV) has not only been important for its hepatotropism and hepatitis development, but also in recent years its association with some forms of non- Hodgkin's lymphoma (NHL), especially B cell NHL, has reported.In some countries, the rate of B cell NHL development in HCV infected patients was four times more than general population, and then association between HCV infection and B-NHL has proposed in many studies...
2014: Iranian Journal of Cancer Prevention
https://read.qxmd.com/read/25034095/gianotti-crosti-syndrome-associated-with-ebstein-barr-virus-and-parvovirus-b-19-coinfection-in-a-male-adult-case-report-and-review-of-the-literature
#52
REVIEW
Jelena Stojkovic-Filipovic, Dusan Skiljevic, Dimitrije Brasanac, Ljiljana Medenica
Gianotti-Crosti syndrome (GCS) is a self-limiting, mostly childhood-appearing, cutaneous eruption with characteristic symmetric areal distribution. The original cases, described by Gianotti in 1955, were associated with hepatitis B virus infection, but other viral and bacterial infections, as well as immunizations, have been implied in etiology of this condition. Adult cases are rare and have been reported almost exclusively in women. We present the case of a 20-year-old Caucasian man who had typical clinical presentation: monomorphic pale, pink-to-flesh - colored or erythematous papules and papulovesicles localized symmetrically over the extensor surfaces of the extremities, buttocks and the face; some lesions were detected on knees, elbows and palms, as well...
February 2016: Giornale Italiano di Dermatologia e Venereologia: Organo Ufficiale, Società Italiana di Dermatologia e Sifilografia
https://read.qxmd.com/read/24779265/-diagnosis-and-prognosis-of-fetal-ebstein-anomaly
#53
JOURNAL ARTICLE
Raúl San Luis-Miranda, Laura G Arias-Mon-roy, Mario Alberto Alcantar-Mendoza, Carlos Cabrera-Arroyo, Edgar Mendoza-Reyes, Silvia Córdova Jarero
BACKGROUND: Fetal echocardiography is possible to confirm with great certainty the diagnosis, in utero, Ebstein's anomaly, as well as determine its perinatal prognosis. OBJECTIVE: Review the experience of 16 cases diagnosed with Ebstein's anomaly, using fetal echocardiography, analyzing "forecast echocardiographic parameters" set by Pavlova, Huhta and Barre. MATERIAL AND METHOD: retrospective and descriptive analysis. We analysed echocardiographic parameters and its correlation with the perinatal development of 16 cases diagnosed with Ebstein's anomaly...
February 2014: Ginecología y Obstetricia de México
https://read.qxmd.com/read/24718007/nasal-t-cell-lymphoma-a-rare-entity
#54
JOURNAL ARTICLE
Maliha Kazi, Mubasher Ikram, Montasir Junaid
Nasal type of Natural Killer (NK)/T cell lymphoma manifests in the nasal cavity. Approximately 95% of them are associated with EBV(Ebstein Barr Virus) with a strong predilection for the Asian population. It has certain systemic and localized symptoms which aid in diagnosis of the condition. However, the histological criteria is pivotal in confirming the diagnosis as well as aiding in confirming the association of EBV. Nasal type of NK/T cell lymphoma has a guarded prognosis. Treatment plan include radiotherapy with concurrent chemotherapy...
March 2014: Journal of the College of Physicians and Surgeons—Pakistan: JCPSP
https://read.qxmd.com/read/24652042/epigenetics-of-multiple-sclerosis-an-updated-review
#55
REVIEW
Cem İsmail Küçükali, Murat Kürtüncü, Arzu Çoban, Merve Çebi, Erdem Tüzün
Multiple sclerosis (MS) is an inflammatory and neurodegenerative disease characterized with autoimmune response against myelin proteins and progressive axonal loss. The heterogeneity of the clinical course and low concordance rates in monozygotic twins have indicated the involvement of complex heritable and environmental factors in MS pathogenesis. MS is more often transmitted to the next generation by mothers than fathers suggesting an epigenetic influence. One of the possible reasons of this parent-of-origin effect might be the human leukocyte antigen-DRB1*15 allele, which is the major risk factor for MS and regulated by epigenetic mechanisms such as DNA methylation and histone deacetylation...
June 2015: Neuromolecular Medicine
https://read.qxmd.com/read/24596757/nasopharyngeal-mucoepidermoid-carcinoma-a-common-entity-at-an-uncommon-location
#56
JOURNAL ARTICLE
A L Hemalatha, Sharath Kumar H K, Geetanjali S, Giripunja M, Shashikumar S D
Mucoepidermoid carcinomas mostly occur in the major salivary glands, the minor salivary glands of oral cavity and in the lacrimal glands. These tumours rarely occur in the sino-nasal tract. When they occur in the sino-nasal tract, the most frequent site is the maxillary antrum, followed by the nasal cavity, the nasopharynx and the ethmoidal sinuses. As per review of literature, nasopharyngeal mucoepidermoid carcinomas account for 0.6% of salivary gland tumours and 4.8% of mucoepidermoid carcinomas. Extensive literature search revealed 21 cases of nasopharyngeal mucoepidermoid carcinomas reported till date...
January 2014: Journal of Clinical and Diagnostic Research: JCDR
https://read.qxmd.com/read/24585919/endobronchial-leiomyoma-in-an-immunocompetent-four-year-old-female-child
#57
JOURNAL ARTICLE
Pallav Gupta, Riti Aggarwal, Prashant Rijal, Krishan Chugh
Pulmonary leiomyoma are uncommonly encountered benign mesenchymal neoplasms in children, usually found in immunosuppressed individuals in association with human immunodeficiency virus or Ebstein-Barr virus infection. We describe an interesting case of a 4-year-old immunocompetent girl who presented with pleural effusion and lung collapse secondary to endobronchial leiomyoma. She underwent a left thoracotomy and a left pneumonectomy for excision of the bronchial mass.
March 2014: Asian Cardiovascular & Thoracic Annals
https://read.qxmd.com/read/24374875/malignancy-and-mortality-in-pediatric-patients-with-inflammatory-bowel-disease-a-multinational-study-from-the-porto-pediatric-ibd-group
#58
MULTICENTER STUDY
Lissy de Ridder, Dan Turner, David C Wilson, Sibylle Koletzko, Javier Martin-de-Carpi, Ulrika L Fagerberg, Christine Spray, Malgorzata Sladek, Ron Shaoul, Eleftheria Roma-Giannikou, Jiri Bronsky, Daniela E Serban, Salvatore Cucchiara, Gabor Veres, Frank M Ruemmele, Iva Hojsak, Kaija L Kolho, Ieuan H Davies, Marina Aloi, Paolo Lionetti, Gigi Veereman-Wauters, Christian P Braegger, Eunice Trindade, Anne V Wewer, Almuthe Hauer, Arie Levine
BACKGROUND: The combination of the severity of pediatric-onset inflammatory bowel disease (IBD) phenotypes and the need for intense medical treatment may increase the risk of malignancy and mortality, but evidence regarding the extent of the problem is scarce. Therefore, the Porto Pediatric IBD working group of ESPGHAN conducted a multinational-based survey of cancer and mortality in pediatric IBD. METHODS: A survey among pediatric gastroenterologists of 20 European countries and Israel on cancer and/or mortality in the pediatric patient population with IBD was undertaken...
February 2014: Inflammatory Bowel Diseases
https://read.qxmd.com/read/24283643/neuralgic-amyotrophy-and-infectious-mononucleosis-a-case-report
#59
JOURNAL ARTICLE
T Esmonde, W Gamble, V Patterson
A 27 year old man developed neuralgic amyotrophy of the right upper limb 5 weeks after an acute febrile illness which was proven serologically to be caused by Ebstein-Barr virus. The weakness developed in a limb that had been used to perform heavy manual labour. A parallel with a similar phenomenon described in association with paralytic poliomyelitis is noted.-
July 1995: European Journal of Neurology
https://read.qxmd.com/read/24060945/recurrent-ebstein-barr-virus-associated-diffuse-large-b-cell-lymphoma-in-an-ascending-aorta-graft
#60
JOURNAL ARTICLE
Crystal R Bonnichsen, Joseph A Dearani, Joseph J Maleszewski, Joseph P Colgan, Eric E Williamson, Naser M Ammash
No abstract text is available yet for this article.
September 24, 2013: Circulation
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