نتایج جستجو برای: pseudolymphoma

تعداد نتایج: 912  

Journal: :Annals of oncology : official journal of the European Society for Medical Oncology 2012
D Soldini E Campo

The current diagnosis of lymphoid neoplasias is based on the criteria of the World Health Organization (WHO) classification. This framework is built on two major principles: the stratification of neoplasms according to their derivation from precursor or mature cells and the definition of clinically relevant nonoverlapping diseases. The diagnosis is established by integrating the clinical, morph...

2015
Takaaki Higashi Daisuke Hashimoto Hiromitsu Hayashi Hidetoshi Nitta Akira Chikamoto Toru Beppu Hideo Baba

Reactive lymphoid hyperplasia (RLH) of the liver is a rare and benign nodular lesion. It remains difficult to distinguish RLH from hepatocellular carcinoma (HCC) despite recent advances in imaging modalities. We report five cases of RLH that required differential diagnosis of HCC preoperatively. These cases all occurred in middle-aged women and were associated with autoimmune disease in 40% (2/...

Journal: :Expert opinion on biological therapy 2008
Anne Galy Maria-Grazia Roncarolo Adrian J Thrasher

BACKGROUND Wiskott Aldrich syndrome (WAS) is a rare X-linked primary immunodeficiency. This complex disease is characterised by microthrombocytopenia, recurrent infections, eczema and is associated with a high incidence of autoimmunity and of lymphoid malignancies. WAS is attracting growing attention not only because it highlights the rich cellular and systems biology revolving around cytoskele...

Journal: :Nihon rinsho. Japanese journal of clinical medicine 1950
M N Manoussakis H M Moutsopoulos

Sjögren's syndrome is a rather common autoimmune disease primarily characterized by the dysfunction and destruction of exocrine glands associated with lymphocytic infiltrations. The disorder has a quite broad clinical presentation, ranging from glandular disease to systemic involvement and to the development of lymphoid malignancy. This article reviews the current aspects in clinical diagnosis ...

Journal: :AJNR. American journal of neuroradiology 1982
G D Hungerford P J Biggs J H Levine B E Shelley P L Perot J K Chambers

Lymphoid hypophysit is is an apparently rare condition whi ch was initially reported as a postmortem finding in six patients [1 -6]. In these patients, death was related to the re latively rapid development of hypopituitarism. It has recently been described in four living patients [7-9]. In the previous case reported by us, visual fi elds were normal and a computed tomography (CT) scan was norm...

Journal: :Blood 1996
W Hiddemann D L Longo B Coiffier R I Fisher F Cabanillas F Cavalli L M Nadler V T De Vita T A Lister J O Armitage

EW INSIGHTS into the pathogenesis of lymphoid maN lignancies have been gained by novel techniques such as genetic, molecular, and immunologic methods and have not only broadened our knowledge about the origin and development of malignant lymphomas, but also have substantial clinical implications. Hence, distinct disorders can be defined more precisely and therapeutic strategies may be directed ...

2018
S Trarieux-Signol D Bordessoule J Ceccaldi S Malak A Polomeni J B Fargeas N Signol H Pauliat S Moreau

BACKGROUND In France, advance directives are favourably perceived by most of the population, although the drafting rate is low. This ambivalence is challenging because advance directives are meant to promote the autonomy and freedom of choice of patients. The purpose of this study was to analyse the content of advance directives written by patients suffering from malignant haemopathies to bette...

Journal: :Blood 2008
Helen Chapel Mary Lucas Martin Lee Janne Bjorkander David Webster Bodo Grimbacher Claire Fieschi Vojtech Thon Mohammad R Abedi Lennart Hammarstrom

The European Common Variable Immunodeficiency Disorders registry was started in 1996 to define distinct clinical phenotypes and determine overlap within individual patients. A total of 7 centers contributed patient data, resulting in the largest cohort yet reported. Patients (334), validated for the diagnosis, were followed for an average of 25.6 years (9461 patient-years). Data were used to de...

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