Results 1 to 10 of about 18,818 (159)

Immunoblastic Lymphadenopathy

JAMA - Journal of the American Medical Association, 1977
Two patients with immunoblastic lymphadenopathy had lymphadenopathy, hepatosplenomegaly, rash, dysproteinemia, constitutional symptoms, and typical morphologic findings of lymph node obliteration by immunoblasts and plasma cells, proliferation of arborizing vessels, and infiltration with amorphous, eosinophilic material.
M, Scheibel, U V, Henriques
exaly   +10 more sources

Reactive Intravascular B-Cell Immunoblastic Proliferation: A Recently Described Entity and a Mimicker of Intravascular Lymphoma

Lymphatics
Reactive intralymphovascular immunoblastic proliferation (ILVIP) is a rare and diagnostically challenging entity that can closely mimic intravascular large B-cell lymphoma (IVLBCL).
Nicolas Ulrich Edgar, Seodam Kwak, Kelsey Baron, Archana Agarwal, Anton Rets, Anna Shestakova   +5 more
doaj   +2 more sources

An Unusual Presentation of Glandular Fever

Case Reports in Infectious Diseases, 2022
Epstein-Barr virus (EBV) is an ubiquitous DNA herpesvirus with >90% of adults >40 years of age showing a serological response. While in their youth, primary EBV infection may pass unnoticed, young adults have a high incidence of infectious mononucleosis (
Dominic Worku, Li Hui Chang, Ian Blyth
doaj   +1 more source

Toxoplasma IgG Expressed in a Patient With Rosai-Dorfman Disease

Kaohsiung Journal of Medical Sciences, 2010
Rosai-Dorfman Disease (RDD) is a rare benign disease characterized by sinus histiocytosis with massive lymphadenopathy. RDD can be differentiated from other types of histiocytosis by immunochemical analysis, as RDD is positive for S100.
Hung-Ju Liao, Ching-Wen Chiang
doaj   +1 more source

Suppurative necrotizing granulomatous lymphadenitis in adult-onset Still’s disease: a case report

Journal of Medical Case Reports, 2012
Introduction Lymphadenopathy is found in about 65% of patients with adult-onset Still’s disease and is histologically characterized by an intense, paracortical immunoblastic hyperplasia. Adult-onset Still’s disease has not been previously described as an
Assimakopoulos Stelios F, Karamouzos Vassilios, Papakonstantinou Christos, Zolota Vassiliki, Labropoulou-Karatza Chryssoula, Gogos Charalambos   +5 more
doaj   +1 more source

KSHV/HHV-8 associated lymph node based lymphomas in HIV seronegative subjects. Case report and review of the literature

Human Pathology: Case Reports, 2016
Extracavitary primary effusion lymphoma (ExPEL) is a rare, high-grade lymphoproliferative disorder that displays immunoblastic, plasmablastic, or anaplastic morphology.
Quyen Nguyen, MD, Parul Bhargava, MD
doaj   +1 more source

Noncaseating suppurative granulomatous lymphadenitis in adult onset Still’s disease – a diagnostic dilemma in a tuberculosis-endemic region: a case report

Journal of Medical Case Reports, 2018
Background Lymphadenopathy is not an uncommon presentation of adult onset Still’s disease: it is present in up to two thirds of patients with adult onset Still’s disease.
S. W. G. J. W. Chinthaka, R. L. Satarasinghe, S. Senanayake, W. A. P. S. R. Weerarathne, A. A. M. Anfaz, M. P. Deraniyagala   +5 more
doaj   +1 more source

Morphology and Immunophenotypes of Canine Lymphomas: a Survey from the Service of Animal Pathology, School of Veterinary Medicine and Animal Science, University of São Paulo, Brazil

Brazilian Journal of Veterinary Pathology, 2011
Lymphoma is a malignant clonal expansion of lymphoid cells, and is reported to be one of the most common hematopoietic neoplasms in dogs. The purpose of this study was to perform a survey of lymphomas diagnosed at the Service of Animal Pathology of the ...
Kátia C. Kimura, Danielle A. Zanini, Adriana T. Nishiya, Ricardo A. Dias, Maria L. Z. Dagli   +4 more
doaj   +1 more source

Immunoblastic lymphadenopathy—report of a case [PDF]

Postgraduate Medical Journal, 1978
Summary A case of immunoblastic lymphadenopathy has been presented which had the characteristic clinical and histological features. The patient did not respond to chemotherapy and succumbed to the disease. Instead of the usual polyclonal gammopathy associated with this condition, he showed a fall in IgM levels, IgG and IgA being within ...
K, Joshi, R, Shrinivasa, S K, Shankar
openaire   +2 more sources

Immunoblastic lymphadenopathy: evolution into immunoblastic sarcoma. [PDF]

Journal of Clinical Pathology, 1979
A case of immunoblastic lymphadenopathy which underwent transformation into immunoblastic sarcoma is reported. A 64-year-old man presented with a rash, generalised lymphadenopathy, and hepatosplenomegaly. A cervical lymph node removed at biopsy showed the features of immunoblastic lymphadenopathy with the presence of heavy chain classes IgG, IgM, and ...
S, Banik, R L, Ward, P S, Hasleton
openaire   +2 more sources