Results 201 to 210 of about 205,932 (232)
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Mediastinal lymphadenopathy due to VEXAS syndrome
BMJ Case ReportsVacuoles, E1 enzyme, X-linked, autoinflammatory, somatic (VEXAS) syndrome is a rare disease first reported in 2020, most commonly seen in men aged 56–75 years old. Common clinical features include skin lesions (83.5%), fever (63.6%), relapsing chondritis (36.4%), venous thrombosis (34.7%) and lymph node enlargement (33.9%).
Jonathan, Burgei +3 more
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MEDIASTINAL LYMPHADENOPATHY IN BUBONIC PLAGUE
American Journal of Roentgenology, 1972V R, Sites, J D, Poland
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[Isolated malignant mediastinal lymphadenopathy].
Revue de pneumologie clinique, 2010Mediastinal adenopathies without pulmonary disease may be benign, lymphomatous or the metastases from intra- or extrathoracic malignancy or more rarely metastases with unknown primary site. We observed 507 patients with isolated mediastinal adenopathies: benign, lymphomatous and metastatic disease represented 41.4% (210/507), 26.8% (136/507), 31.8 ...
M, Riquet +5 more
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Tuberculous mediastinal lymphadenopathy
Journal of the Korean Radiological Society, 1973JH Park, KS Kim, CW Kim
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Proteinaceous Lymphadenopathy: A Rare Cause of Mediastinal Lymphadenopathy
Chest, 2016Rabin Shrestha, Dipen Kadaria
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Case Report: Sinus Histiocytosis With Massive Lymphadenopathy
Ca-A Cancer Journal for Clinicians, 1980David Kelly +2 more
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