Results 31 to 40 of about 24,724 (311)

Spatial Signatures Identify Immune Escape via PD-1 as a Defining Feature of T-cell/Histiocyte-rich Large B-cell Lymphoma.

Blood, 2020
T-cell/histiocyte-rich large B cell lymphoma (TCRLBCL) is an aggressive variant of diffuse large B cell lymphoma (DLBCL) characterized by rare malignant B cells within a robust but ineffective immune cell infiltrate.
G. Griffin, Jason L. Weirather, M. Roemer, M. Lipschitz, Alyssa Kelley, Pei-Hsuan Chen, D. Gusenleitner, Erin Jeter, Christine J. Pak, E. Gjini, B. Chapuy, M. Rosenthal, Jie Xu, Benjamin J Chen, A. Sohani, S. Lovitch, J. Abramson, J. Ishizuka, A. Kim, C. Jacobson, A. LaCasce, C. Fletcher, D. Neuberg, G. Freeman, F. Hodi, Kyle T. Wright, A. Ligon, E. Jacobsen, P. Armand, M. Shipp, S. Rodig   +30 more
semanticscholar   +1 more source

Nodular lymphocyte-predominant Hodgkin lymphoma with nodules resembling T-cell/histiocyte-rich B-cell lymphoma: differential diagnosis between nodular lymphocyte-predominant Hodgkin lymphoma and T-cell/histiocyte-rich B-cell lymphoma

Blood, 2003
Jan Delabie
exaly   +2 more sources

Nodular histiocytic/mesothelial hyperplasia, a benign entity posing diagnostic challenge

Human Pathology Reports, 2022
Nodular histiocytic/mesothelial hyperplasia (NHMH) is a benign entity that can simulate malignancies histologically. NHMH was initially described in 13 hernia sacs in 1975.
Hasan Basri Aydin, Anne Chen, Hwajeong Lee   +2 more
doaj   +1 more source

T cell/histiocyte rich B-cell lymphoma: A difficult diagnosis to make

Current Problems in Cancer: Case Reports, 2020
Diffuse large B-cell lymphoma (DLBCL) is the most common type of non-Hodgkin lymphoma. Rarely, DLBCL appears on a background of T-cell and histiocyte-rich stroma, referred to as T-cell/histiocyte rich large B cell lymphoma (T/HRBCL).
Olutayo A. Sogunro, Rachael Steinhauer, Eugene Lewis   +2 more
doaj   +1 more source

Effect of platelet-rich plasma on postoperative peritoneal inflammation and adhesions

Archives of Medical Science, 2020
Introduction Postoperative peritoneal adhesion is an important complication of abdominopelvic surgery. The aim of this study is to reveal the effect of platelet-rich plasma (PRP) on postoperative intraperitoneal inflammation and adhesions.
Dursun Özgür Karakaş, Özgür Dandin, Tuba Müftüoğlu, Deniz Tihan, Ahmet Selim Bal, Şükrü Yıldırım   +5 more
doaj   +1 more source

Langerhans cell histiocytosis

Клинический разбор в общей медицине, 2023
Langerhans cell histiocytosis is a rare proliferative disease of histiocyte-like cells, the peak incidence of which occurs in early childhood. Pulmonary Langerhans Cell Histiocytosis is one of the forms of this disease, but it usually affects young ...
Victor V. Fomin, Maria I. Mitkina, Elena N. Popova , Liubov A. Ponomareva , Alina A. Chinova   +4 more
doaj   +1 more source

Community Acquired Pneumonia Associated Fatal Secondary Hemophagocytic Lymphohistiocytosis Syndrome

The Journal of Association of Chest Physicians, 2018
The burden of community-acquired pneumonia (CAP) requiring hospitalization among adults is substantial and is a leading infectious cause of hospitalization and death. Severe CAP may rarely get complicated with secondary hemophagocytic lymphohistiocytosis
Arun Agarwal, Mudit Agarwal
doaj   +1 more source

Spontaneous pneumothorax with pulmonary Langerhans cell histiocytosis (PLCH) in an adult heavy cigarette smoker—A case report

Respirology Case Reports, 2022
Pulmonary Langerhans cell histiocytosis is a rare disease caused by the proliferation of CD1a‐positive histiocyte‐like cells infiltrating the lung's interstitial layer.
Chiao‐Yun Tsai, Hsu‐Chih Huang, Zhen‐Dong Xu, Jiun‐Yi Hsia, Chih‐Yi Chen   +4 more
doaj   +1 more source

Genetic lesions in nodular lymphocyte-predominant Hodgkin lymphoma and T cell/histiocyte-rich large B-cell lymphoma identified by whole genome sequencing. [PDF]

Leukemia
Rausch T, Schäfer H, Bein J, Mölder F, Beeck LK, Kölsch B, Borchert S, Benes V, Halbsguth T, Brunnberg U, Oellerich T, Tousseyn T, Ponzoni M, Köster J, Hansmann ML, Küppers R, Hartmann S.   +16 more
europepmc   +2 more sources

Histiocyte disorders [PDF]

British Medical Bulletin, 1996
Histiocyte disorders are characterised by tissue infiltration with cells of monocyte/macrophage lineage, with two disorders, Langerhans' cell histiocytosis (LCH) and haemophagocytic lymphohistiocytosis (HLH) accounting for the overwhelming majority of cases in childhood and, apart from monocyte variants of acute myeloid leukaemia, histiocytic ...
openaire   +2 more sources