Results 141 to 150 of about 24,507 (317)

T-zone histiocytes in adenocarcinoma of the lung in relation to postoperative prognosis [PDF]

open access: bronze, 1985
T Furukawa   +5 more
openalex   +1 more source

Mycosis Fungoides, Sézary Syndrome, and Cutaneous B‐Cell Lymphomas: 2025 Update on Diagnosis, Risk‐Stratification, and Management

open access: yesAmerican Journal of Hematology, Volume 100, Issue 9, Page 1603-1628, September 2025.
ABSTRACT Disease Overview Primary cutaneous lymphomas are a rare and heterogeneous group of extranodal lymphomas that require the integration of clinical and histopathologic data for classification and treatment. Diagnosis Diagnosis and disease classification is based on histopathologic review and immunohistochemical staining of an appropriate skin ...
Alexandra C. Hristov   +2 more
wiley   +1 more source

How I diagnose and treat splenic lymphomas. [PDF]

open access: yes, 2011
The incidental finding of an isolated splenomegaly during clinical assessment of patients evaluated for unrelated causes has become increasingly frequent because of the widespread use of imaging.
Iannitto, E, TRIPODO, Claudio
core  

Histiocytes in nasopharyngeal carcinoma in relation to prognosis [PDF]

open access: bronze, 1986
Hiroaki Nomori   +4 more
openalex   +1 more source

Association Between Moraxella catarrhalis and Nodular Lymphocyte‐Predominant Hodgkin Lymphoma

open access: yesAmerican Journal of Hematology, Volume 100, Issue 9, Page 1543-1556, September 2025.
ABSTRACT Nodular lymphocyte‐predominant Hodgkin Lymphoma (NLPHL) may be an antigen‐driven malignancy. Recent studies demonstrated that in NLPHL patients, lymphoma B‐cell receptor can bind proteins derived from Moraxella catarrhalis (MC) and Rothia mucilaginosa (RM). We examined whether MC and RM can be detected in NLPHL lymph nodes.
Izidore S. Lossos   +7 more
wiley   +1 more source

Multisystem Langerhans' cell histiocytosis (Hand-Schüller-Christian disease) in an adult: a case report and review of the literature [PDF]

open access: yes, 2018
Langerhans' cell histiocytosis (LCH) is a rare and enigmatic clonal disorder that affects mainly children. It is characterized by single or multiple granulomatous mass lesions composed of cells with the Langerhans' cell phenotype.
Jaques, B.   +3 more
core  

Macrophage-histiocytes in malignant lymphoma, small lymphocytic type (well-differentiated lymphocytic lymphoma) [PDF]

open access: bronze, 1985
H. J. Ree   +2 more
openalex   +1 more source

Cytological Assessment of Metastatic Gastrointestinal Stromal Tumor in Ascitic Fluid

open access: yesDiagnostic Cytopathology, Volume 53, Issue 9, Page 462-465, September 2025.
ABSTRACT Gastrointestinal stromal tumors (GISTs) are mesenchymal neoplasms typically arising in the stomach and small intestine and rarely involving extra‐gastrointestinal organs. While fine‐needle aspiration (FNA) offers reliable diagnosis, exfoliation of GIST cells into body fluids is exceedingly rare and diagnostically challenging.
Hadi Sultan   +4 more
wiley   +1 more source

Histopathological Patterns of Cutaneous and Mucocutaneous Leishmaniasis Due to L. aethiopica

open access: yesDermatology Research and Practice
Conclusion: In our study, the histopathological patterns of the CL caused by L. aethiopica were shown to have a dermal change that was characterized by a domination of diffused inflammatory cell infiltrate.
Abay Atnafu   +7 more
doaj   +1 more source

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