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
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 +4 more
doaj +1 more source
A practical algorithmic approach to mature aggressive B cell lymphoma diagnosis in the double/triple hit era. Selecting cases, matching clinical benefit. A position paper from the Italian Group of Haematopathology (G.I.E.) [PDF]
, 2019 An accurate diagnosis of clinically distinct subgroups of aggressive mature B cell lymphomas is crucial for the choice of proper treatment. Presently, precise recognition of these disorders relies on the combination of morphological, immunophenotypical ...
Agostinelli, C. +17 more
core +2 more sources
Nodular lymphocyte predominant Hodgkin lymphoma behaves as a distinct clinical entity with good outcome: evidence from 14-year followup in the West of Scotland Cancer Network [PDF]
, 2011 Clinically and biologically, nodular lymphocyte predominant Hodgkin lymphoma (NLPHL) has much more in common with germinal-center derived B-cell non-Hodgkin lymphoma (NHL) than with classical Hodgkin lymphoma (cHL).
Diehl V +8 more
core +1 more source
Leukemia and Lymphoma, 2019 Using data from the National Cancer Data Base, 2010–2015, we examined characteristics and outcomes of T-cell/histiocyte-rich large B-cell lymphoma (THRLBCL, N = 622) relative to unspecified diffuse large B-cell lymphoma (DLBCL-NOS, N = 91,588) and ...
T. Ollila, J. Reagan, A. Olszewski
semanticscholar +1 more source
A Previously Unrecognized Granulomatous Variant of Gamma-Delta T-Cell Lymphoma
Dermatopathology, 2021 Primary cutaneous γδ T-cell lymphoma (PCGD-TCL) is an extremely rare and aggressive T-cell neoplasm with complex heterogeneity. We present a series of two patients who presented with firm, subcutaneous nodules and were diagnosed with PCGD-TCL.
Tatsiana Pukhalskaya +3 more
doaj +1 more source
Cytometry. Part B, Clinical cytometry, 2019 T‐cell/histiocyte rich large B‐cell lymphoma (THRLBCL) is B‐cell lymphoma in which rare neoplastic cells are embedded in a reactive infiltrate. We describe the first characterization of the neoplastic cells by flow cytometry (FC).
E. Glynn, J. Fromm
semanticscholar +1 more source
Anais Brasileiros de Dermatologia, 2003 Atualmente, os histiócitos não são mais compreendidos como células únicas, mas como um grupo heterogêneo de células com o mesmo aspecto histológico, mas com características e funções distintas entre si.
Flávio Barbosa Luz +3 more
doaj +1 more source
T-cell/histiocyte-rich large B-cell lymphoma presenting as a primary central nervous system lymphoma
Rare 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 +1 more source
Chromosome Condensation 1-Like (Chc1L) Is a Novel Tumor Suppressor Involved in Development of Histiocyte-Rich Neoplasms. [PDF]
PLoS 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 +1 more source