Results 1 to 10 of about 25,153 (346)

Nodular Lymphocyte Predominant Hodgkin Lymphoma and T Cell/Histiocyte Rich Large B Cell Lymphoma - Endpoints of a Spectrum of One Disease? [PDF]

open access: yesPLoS ONE, 2013
In contrast to the commonly indolent clinical behavior of nodular lymphocyte predominant Hodgkin lymphoma (NLPHL), T cell/histiocyte rich large B cell lymphoma (THRLBCL) is frequently diagnosed in advanced clinical stages and has a poor prognosis ...
Sylvia Hartmann   +2 more
exaly   +5 more sources

T-cell/histiocyte-rich large B-cell lymphoma presenting as a primary central nervous system lymphoma [PDF]

open access: goldRare Tumors, 2015
Primary central nervous system (PCNSL) lymphoma is an aggressive extranodal non-Hodgkin lymphoma, and most cases are classified as diffuse large B-cell lymphoma (DLBCL) by histology.
Pooja Advani   +6 more
doaj   +2 more sources

Chromosome Condensation 1-Like (Chc1L) Is a Novel Tumor Suppressor Involved in Development of Histiocyte-Rich Neoplasms. [PDF]

open access: goldPLoS ONE, 2015
Human chromosomal region 13q14 is a deletion hotspot in prostate cancer, multiple myeloma, and chronic lymphocytic leukemia. This region is believed to host multiple tumor suppressors. Chromosome Condensation 1-like (CHC1L) is located at 13q14, and found
David R Spillane   +9 more
doaj   +3 more sources

Diagnosis of Rosai-Dorfman Disease by Fine Needle Aspiration Cytology in a Case with Cervical Lymphadenopathy and Nasal Mass [PDF]

open access: yesOnline Journal of Health & Allied Sciences, 2011
We report a case of Rosai-Dorfman Disease, a rare non neoplastic proliferative disorder of the cells of macrophage-histiocyte family, in a case with cervical lymphadenopathy and nasal mass diagnosed by fine needle aspiration cytology.
Madhusmita Jena
doaj   +2 more sources

Histiocyte Society blueprint for hemophagocytic lymphohistiocytosis research: deciphering underlying disease mechanisms to optimize diagnosis and therapy [PDF]

open access: yesHaematologica
Hemophagocytic lymphohistiocytosis (HLH) is a rare syndrome characterized by severe hyperinflammation, leading to endorgan damage and death in the absence of treatments directed at suppressing the overactive immune system.
Lauren K. Meyer   +3 more
doaj   +2 more sources

Langerhans Cell Histiocytosis with Temporal Bone Involvement- A Case Report [PDF]

open access: yesInternational Journal of Anatomy Radiology and Surgery, 2021
Langerhans Cell Histiocytosis (LCH) is a rare disorder of the reticuloendothelial system associated with proliferation of Langerhans cells and mature eosinophils.
VISHWANATH VIJAY JOSHI   +4 more
doaj   +1 more source

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