Results 71 to 80 of about 841,085 (164)

Hemangioma glomeruloide e a síndrome POEMS: relato de dois casos e revisão da literatura Glomeruloid hemangioma in POEMS syndrome: a report on two cases and a review of the literature

open access: yesAnais Brasileiros de Dermatologia, 2011
O hemangioma glomeruloide caracteriza-se por enovelados capilares contidos em espaços vasculares dilatados reminiscentes de glomérulos renais, sendo fortemente associado à síndrome POEMS (polineuropatia, organomegalia, endocrinopatia, gamopatia ...
Thiago Jeunon   +4 more
doaj   +1 more source

Sentinel Lymph Node in Endometrial Hyperplasia: State of the Art and Future Perspectives [PDF]

open access: yes
Background/Objectives: Endometrial hyperplasia is a uterine pathology characterized by the abnormal proliferation of endometrial glands, resulting in an increased gland-to-stroma ratio.
Luigi Della Corte   +35 more
core   +2 more sources

Simultaneous lymph node involvement by Castleman disease and Kaposi sarcoma

open access: yesRevista Brasileira de Hematologia e Hemoterapia, 2011
Both multicentric Castleman disease and Kaposi sarcoma are more frequently observed in HIV infected patients. The coexistence of these Human herpesvirus 8 related lesions, in the same tissue, has been observed, but literature reports are scant.
Luciana Wernersbach Pinto   +1 more
doaj   +1 more source

LYMPHOGRAPHY IN MEDIASTINAL LYMPH NODE HYPERPLASIA

open access: yes, 2017
In two cases of mediastinal lymph node hyperplasia lymphography was performed in an attempt to evaluate the retioperitoneal lymphatic system. Since the lymphograms show the non-spec pattern of lymphoid hyperplasia, they do not allow a differential ...
Sako, M   +3 more
core  

Castleman Disease of the Parapharyngeal Space in a Pediatric Patient: A Case Report

open access: yesEar, Nose & Throat Journal
The Castleman Disease (CD), also recognized as giant lymph node hyperplasia or vascular follicular lymphoid hyperplasia, is an infrequent lymphoproliferative disorder with substantial clinical variability.
Xin Wang MD   +3 more
doaj   +1 more source

Doença de Castleman ou hiperplasia angiofolicular como nódulo pulmonar solitário: relato de caso Castleman disease or angiofollicular hyperplasia as a solitary pulmonary nodule: case report

open access: yesJornal Brasileiro de Pneumologia, 2007
Doença de Castleman é uma doença rara que se manifesta geralmente como nódulo mediastinal, com grande variabilidade de apresentação em relação a idade, manifestações clínicas e evolução.
Guilherme Andrade Krawczun   +4 more
doaj   +1 more source

Impact of siltuximab on patient-related outcomes in multicentric Castleman’s disease

open access: yesPatient Related Outcome Measures, 2018
Jenna Sitenga,1 Gregory Aird,1 Aabra Ahmed,1 Peter T Silberstein2 1Division of Education, Creighton University School of Medicine, Omaha, NE, USA; 2Division of Hematology/Oncology, Creighton University School of Medicine, Omaha, NE, USA Abstract ...
Sitenga J   +3 more
doaj  

Multicentric giant lymph node hyperplasia: an immunohistochemical study.

open access: yes, 1983
Biopsy specimens from five cases of multicentric giant lymph node hyperplasia were studied by standard histochemical techniques and by immunoperoxidase staining and double immunoenzyme labeling to determine the distribution of intracytoplasmic ...
MASSARELLI, Giovannino   +2 more
core  

Inflammation induced by different plasmid types of russian Yersinia pseudotuberculosis strains

open access: yesИнфекция и иммунитет, 2019
In the 2000s, a scientific interest to the Far Eastern scarlet-like fever (FESLF) mainly recorded In Russia and Japanwas remarkably increased. Such clinical and epidemic manifestation of human pseudotuberculosis is related to a certain bacterial clonal ...
L. M. Somova   +4 more
doaj   +1 more source

Growth failure, refractory anaemia and hypergammaglobulinaemia: their regression after removal of a mesenteric tumour with the features of giant lymph node hyperplasia, plasma-cell type

open access: yes, 1978
The authors report the case of a 15-year-old boy with longstanding anemia, polyclonal hypergammaglobulinemia and growth retardation with absence of growth hormone secretion.
Wolter, Renee Adrienne   +3 more
core  

Home - About - Disclaimer - Privacy