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Tuberculous Mediastinal Lymphadenopathy
Acta Clinica Belgica, 1998We report about 2 cases of isolated mediastinal tuberculous lymphadenitis presenting without parenchymal infiltrates. Although rare, this mode of presentation reminds the clinician that tuberculosis has to be included in the differential diagnosis of mediastinal masses even in the absence of parenchymal lesion.
P, Hainaut +3 more
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Tuberculous mediastinal lymphadenopathy in Bradford
Clinical Radiology, 1980During the calendar year 1978, 18 patients who commenced treatment for pulmonary tuberculosis in the Bradford Chest Clinic were found to have enlarged mediastinal lymph glands. Sixteen of these 18 patients were adults who thus presented radiographic patterns which have been classically regarded are representing primary tuberculous infection and are ...
H C, Irving, T S, Brown
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Osteosarcoma with calcific mediastinal lymphadenopathy
Pediatric Radiology, 1987A case of osteosarcoma with calcific mediastinal lymphadenopathy is presented. The lesion caused increasing dysphagia and bronchial erosion, showed uptake of isotope on a bone scan and was seen to enlarge on follow-up CT scans.
T E, van Zanten +2 more
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Tuberculous Mediastinal Lymphadenopathy in Adults
Radiology, 1978Three cases of paratracheal and hilar lymph node enlargement without parenchymal lung lesion simulating sarcoidosis, lymphoma, and metastasis were finally proved to be tuberculous lymphadenitis. Although it is not a common manifestation of tuberculous infection in the adult, this possibility should be considered in the differential diagnosis of ...
C I, Liu, W R, Fields, C I, Shaw
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Anterior mediastinal lymphadenopathy in sarcoidosis
American Journal of Roentgenology, 1976Several lymph node chains in the anterior mediastinum lie between the sternum and the trachea. On a lateral chest radiograph they form two distinct groups separated by the superior vena cava. One group projects anterior to the trachea and is formed by overlapping nodes of the anterior paratracheal and the left anterior mediastinal (prearterial) chains.
Y M, Berkmen, B R, Javors
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Mediastinal lymphadenopathy: differential diagnosis challenges
Russian Journal of Preventive Medicine, 2023The leading causes of mediastinal lymphadenopathy are briefly described, and a clinical case is presented that demonstrates the difficulty of differential diagnosis of mediastinal lymphadenopathy in a patient with a nonspecific presentation. The unique feature of this case is the detection of granulomatous inflammation typical for tuberculosis in the ...
I.V. Demko +6 more
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2019
Lymphadenopathy represents the pathologic enlargement of lymph nodes. Within the chest, the mediastinum is the most commonly affected region. Mediastinal lymphadenopathy may result in loss of normal mediastinal contours or thickening of lines and stripes.
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Lymphadenopathy represents the pathologic enlargement of lymph nodes. Within the chest, the mediastinum is the most commonly affected region. Mediastinal lymphadenopathy may result in loss of normal mediastinal contours or thickening of lines and stripes.
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Mediastinal Lymphadenopathy in Children With Histoplasmosis
Journal of Surgical Research, 2019Mediastinal lymphadenopathy (ML) in children can arise from malignancy, infection, or rheumatic illness among others, and may be found incidentally on imaging or during workup for a variety of symptoms. Our aim was to describe the clinical presentation and natural history of histoplasmosis in children who present to a tertiary care center with ML in an
Jessica K, Staszak +4 more
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Sarcoidosis presenting with posterior mediastinal lymphadenopathy
Postgraduate Medicine, 1982A young man with exertional dyspnea, maculopapular skin lesions, and generalized lymphadenopathy was found to have a posterior mediastinal density on a chest roentgenogram. Sarcoidosis was diagnosed on the basis of lymph node and skin biopsy findings, and corticosteroid therapy was started. After six months of treatment the patient was free of symptoms
C P, Kutty, B, Varkey
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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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