Results 11 to 20 of about 623,470 (191)
Castleman's Disease: A Case Report of the Unicentric Type
Castleman's disease, or angiofollicular lymph node hyperplasia, is a relatively rare disorder characterized by the benign proliferation of lymphoid tissue related to the chronic human herpes virus 8 (HHV-8) infection and the human immunodeficiency virus (
J. Gomez-Ramirez +7 more
doaj +2 more sources
Video assisted thoracoscopic resection of a posterior mediastinal Castleman's tumor [PDF]
Castleman's disease (CD) or angiofollicular lymph node hyperplasia is a rare spectrum of lymphoproliferative disorders. CD tumors are commonly localized in the mediastinum and are usually asymptomatic.
Panait Lucian +3 more
doaj +4 more sources
Castleman's disease. A case report
Angiofollicular lymph node hyperplasia or Castleman's Disease (CD) is a rare lymphoproliferative disorder that manifests itself as a local or generalized tumor-like condition affecting both lymph nodes and non-nodal tissues, usually in the chest ...
D Arslan +4 more
doaj +4 more sources
Background: Castleman’s disease (CD), also known as angiofollicular lymph node hyperplasia, describes a rare group of diseases manifesting with enlarged lymph nodes and various inflammatory symptoms.
Walid Kteiche +7 more
doaj +2 more sources
Kaposi's sarcoma of lymph nodes associated with multicentric angiofollicular hyperplasia.
A case of multicentric angiofollicular hyperplasia (hyaline-vascular type) associated with Kaposi sarcoma of lymph nodes is reported. The patient was a 75-year-old man who suffered from edema, fever, maculopapular skin rashes and polyclonal hypergammaglo-bulinemia and died 10 days after admission to hospital for acute tubular necrosis and pulmonary ...
Leoncini, L +4 more
core +4 more sources
Idiopathic Multicentric Castleman Disease With Severe Eosinophilia and Diffuse Centrilobular Nodule-A Rare Case Report. [PDF]
Rationale Idiopathic multicentric Castleman disease (iMCD), also known as angiofollicular lymph node hyperplasia, is a rare inflammatory lymphoproliferative disease with diverse clinical presentations. We report a rare case of iMCD accompanied by severe eosinophilia and diffuse centrilobular pulmonary nodules, which have rarely been previously ...
Li X +6 more
europepmc +2 more sources
Idiopathic Multicentric Castleman Disease Associated With Seronegative Erosive Chronic Polyarthritis: A Diagnostic Challenge [PDF]
ABSTRACT Idiopathic multicentric Castleman disease can rarely present with systemic inflammation and erosive seronegative polyarthritis. Awareness of this association helps prevent misdiagnosis and ensures appropriate immunosuppressive management based on clinicopathological and immunohistochemical correlation.
Lo B +9 more
europepmc +2 more sources
A Case of Angiofollicular Lymph Node Hyperplasia [PDF]
A case of mediastinal lymph node hyperplasia with angiofollicular predominance is presented. Three years before operation the mediastinal process was discovered at routine chest X-ray. The patient, a 23-year-old woman, had no symptoms whatsoever. The specific nature of the process was revealed on histopathoiogical examination.
C, Sundström, T, Aberg
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Angiofollicular lymph node hyperplasia (Castleman) [PDF]
Six personally observed cases of this lesion are reported and the literature is reviewed. One hundred and thirty-four cases have been reported to date. The lesion has occurred in many sites, but is commonest in the thorax (60%), abdomen (11%), neck (14%), and axilla (4%). Ninety per cent of cases are symptomless or have only the pressure
D, Anagnostou, C V, Harrison
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Angiofollicular lymph node hyperplasia with amyloidosis [PDF]
Abstract Two cases of angiofollicular lymph node hyperplasia are described, one of the solitary plasma cell type the other of the multicentric hyaline vascular type. Both cases illustrate the wide ranging clinical and pathological findings associated with this condition but both also have unusual features. The solitary plasma cell lesion
K P, West, D R, Morgan, I, Lauder
openaire +2 more sources

