نتایج جستجو برای: malignant lymphoproliferative

تعداد نتایج: 217789  

Journal: :Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2005
Kei Matsushita Kiyotaka Nagahama Yoshiaki Inayama Katsumichi Fujimaki Kouichi Tamura Nobuhito Hirawa Minoru Kihara Yoshiyuki Toya Machiko Yabana Kensuke Joh Satoshi Umemura

Sir, Fibrillary glomerulonephritis (FGN) and immunotactoid glomerulopathy (ITG) are well known glomerular diseases with Congo-red-negative deposits [1–4]. While FGN is characterized by randomly arranged microfibrils around 20 nm in diameter with no underlying systemic disorder, ITG is defined by orderly arranged microtubular deposits, usually >30nm in diameter with a hollow core; patients with ...

2013
Saime Paydaş Semra Paydaş Mustafa Balal Arbil Açıkalın Melek Ergin Emel Gürkan Fikri Başlamışlı

UNLABELLED Posttransplant malignancy is one of the most important complications of organ transplantation. Immunosuppressive drugs, viral infections such as human herpes virus 8 or Epstein-Barr virus, exposure to carcinogenic factors such as sun, and host factors can be etiologic factors in the development of malignant disease. In this paper we report 2 cases of late posttransplant lymphoprolife...

2014
Jia WANG Xi XIE Fen LI Jinwei CHEN

©2014 Turkish League Against Rheumatism. All rights reserved. Patients with rheumatic diseases are at an increased risk for malignant lymphoproliferative disease, but the coexistence of rheumatic diseases and multiple myeloma is uncommon. Herein, we report a rare case of systemic lupus erythematosus and Sjögren's syndrome, which preceded the development of multiple myeloma after three years. We...

Journal: :Acta dermato-venereologica 2010
Takashi Masu Ryuhei Okuyama Takahiko Tsunoda Takashi Hashimoto Setsuya Aiba

© 2010 The Authors. doi: 10.2340/00015555-0739 Journal Compilation © 2010 Acta Dermato-Venereologica. ISSN 0001-5555 Sir, Paraneoplastic pemphigus (PNP) is an autoimmune bullous disease characterized by severe mucous membrane involvement, polymorphous skin eruptions, and underlying neoplasms. Most cases are associated with lymphoproliferative neoplasms, and solid tumours have rarely been associ...

Journal: :Annals of clinical and laboratory science 2002
James Harris Daniel Cherry John Lazarchick

Extracellular, PAS-positive material has been described in various lymphoproliferative disorders, but is rare in malignant lymphomas. We report two such cases of grade 2 follicular lymphoma that were investigated by routine H&E histology, immunohistochemistry, flow cytometry, and molecular pathology. Ancillary studies confirmed the monoclonality in each case and the antigenic similarity to the ...

2015
Erica Sbrissa Estela Risso Maria Elisa Andrade João Ferreira De Mello Cintia Bassani Dayane Brandini Tatiana Mercuri De Campos

Background Nodular lymphoid hyperplasia (NLH) of intestine is an extremely rare lymphoproliferative disorder of uncertain etiology. Usually, polyps benign lymphoid tissue are present in the intestinal mucosa. It may present as an asymptomatic or manifest with gastrointestinal symptoms such as abdominal pain, chronic diarrhea, occult bleeding or intestinal obstruction. NLH found in association w...

Journal: :Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 1996
M F Mamzer-Bruneel C Legendre O Hermine G Flandrin B Varet H Kreis

Hairy-cell leukaemia is a rather uncommon chronic malignant lymphoproliferative disorder accounting for about 2% of all adult leukaemia cases [1]. This clonal B-cell proliferation [2] is characterized by a cellular infiltration of both bone marrow and spleen by large differentiated B cells, often exhibiting hair-like protrusions (hairy cells). We report here the first case of hairy-cell leukaem...

2005
Jin-Wuk Hur Hye-Soon Lee Wan-Sik Uhm Jae-Bum Jun Sang-Cheol Bae Chan-Kum Park Dae-Hyun Yoo

Eosinophilic fasciitis (EF) is scleroderma-like disease without Raynaud's phenomenon or visceral involvement. It is characterized by painful swelling of the extremities, accompanied by rapid weight gain, fever and myalgia. The acute state of disease is associated with significant peripheral blood eosinophilia, an elevated erythrocyte sedimentation rate and hypergammaglobulinemia. EF is also fre...

Journal: :Journal of cell science 2016
Dong Wang Jingyu Chen Rui Li Guolin Wu Zimin Sun Zhitao Wang Zhimin Zhai Fang Fang Yugang Guo Yongjun Zhong Ming Jiang Huan Xu Minhua Chen Guodong Shen Jie Sun Bailing Yan Chundong Yu Zhigang Tian Weihua Xiao

Paired box protein 5 (PAX5) plays a lineage determination role in B-cell development. However, high expression of PAX5 has been also found in various malignant diseases, including B-lymphoproliferative disorders (B-LPDs), but its functions and mechanisms in these diseases are still unclear. Here, we show that PAX5 induces drug resistance through association and activation of receptor-interactin...

Journal: :Therapeutische Umschau. Revue therapeutique 2004
A Gähler S Cogliatti W Korte

The differential diagnosis of absolute lymphocytosis is variegated. In general, reactive (secondary) lymphocytosis can be well differentiated from a lymphoproliferative disease (primary lymphocytosis). Together with correspondent clinical characteristics, an absolute lymphocytosis often suggests a potential diagnosis and the further diagnostic process. Reactive lymphocytosis is usually self lim...

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