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Dysphagia due to mediastinal tuberculous lymphadenitis presenting as an esophageal submucosal tumor: a case report
Yonsei Medical Journal ; : 386-391, 1995.
Article in English | WPRIM | ID: wpr-40544
ABSTRACT
Mediastinal tuberculous lymphadenitis is rare in adults, and it is even rarer for dysphagia to be the presenting symptom of mediastinal tuberculous lymphadenitis. Mediastinal tuberculous lymphadenitis with esophageal symptoms has been presented as esophageal ulceration, mucosal or submucosal mass with ulceration, fistula or sinus formation, extrinsic compression, or displacement of the esophagus. An exaggerated form of extrinsic compression may be presented as a submucosal tumor, radiologically or endoscopically. A barium esophagography of a 34 year-old woman with painful dysphagia revealed a large submucosal tumor-like mass on the mid-esophagus. The symptom was spontaneously improved over a 3-week period together with reduction of the mass size. A computed tomography of the chest disclosed an enlarged subcarinal lymph node and histologic examination of the specimen obtained by thoracoscopic biopsy brought about a diagnosis of tuberculosis. We herein report a case of mediastinal tuberculosis with unusual manifestations.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Tuberculosis, Lymph Node / Esophageal Neoplasms / Radiography, Thoracic / Deglutition Disorders / Tomography, X-Ray Computed / Esophagoscopy / Diagnosis, Differential / Esophagus / Mediastinal Diseases Type of study: Diagnostic study Limits: Adult / Female / Humans Language: English Journal: Yonsei Medical Journal Year: 1995 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Tuberculosis, Lymph Node / Esophageal Neoplasms / Radiography, Thoracic / Deglutition Disorders / Tomography, X-Ray Computed / Esophagoscopy / Diagnosis, Differential / Esophagus / Mediastinal Diseases Type of study: Diagnostic study Limits: Adult / Female / Humans Language: English Journal: Yonsei Medical Journal Year: 1995 Type: Article