1.A Case of Conservatively Resolved Intramural Esophageal Dissection Combined with Pneumomediastinum.
In Hye CHA ; Jin Nam KIM ; Sun Ok KWON ; Sun Young KIM ; Myoung Ki OH ; Soo Hyung RYU ; You Sun KIM ; Jeong Seop MOON
The Korean Journal of Gastroenterology 2012;60(4):249-252
Intramural esophageal dissection (IED) is a rare form of esophageal injury. We report a rare case of spontaneous IED complicated with pneumomediastinum and successfully improved by conservative management. A 46-year-old man presented to the emergency department with chest pain and hematemesis. The endoscopic diagnosis was suspicious of IED. Chest CT scan performed to rule out complication noted IED combined with pneumomediastinum. He was managed conservatively with nil per oral, intravenous antibiotics and parenteral nutrition. Follow up study after 2 weeks later showed near complete resolution of IED. IED should be included in the differential diagnosis for unexplained acute chest pain, especially, associated with dysphagia and hematemesis. IED with pneumomediastinum or mediastinitis require prompt surgery. So far, there is no case report of IED combined with pneumomediastinum which resolved without surgical treatment. In this case, IED combined with pneumomediastinum has improved by conservative management, so we present a case report.
Anti-Bacterial Agents/therapeutic use
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Esophageal Diseases/complications/*diagnosis/drug therapy
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Gastroscopy
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Hematemesis/complications/diagnosis
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Humans
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Male
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Mediastinal Emphysema/complications/*diagnosis/drug therapy
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Middle Aged
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Tomography, X-Ray Computed
2.Dysphagia due to mediastinal tuberculous lymphadenitis presenting as an esophageal submucosal tumor: a case report.
Seung Ho PARK ; Jun Pyo CHUNG ; In Jae KIM ; Hyo Jin PARK ; Kwan Sik LEE ; Chae Yoon CHON ; In Suh PARK ; Ki Whang KIM ; Doo Yun LEE
Yonsei Medical Journal 1995;36(4):386-391
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.
Adult
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Case Report
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Deglutition Disorders/*etiology
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Diagnosis, Differential
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Esophageal Neoplasms/*diagnosis
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Esophagoscopy
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Esophagus/pathology/radiography
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Female
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Human
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Mediastinal Diseases/*complications/*diagnosis
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Radiography, Thoracic
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Tomography, X-Ray Computed
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Tuberculosis, Lymph Node/*complications/*diagnosis
3.Spontaneous Pneumomediastinum: A Rare Disease Associated with Chest Pain in Adolescents.
Sung Hoon KIM ; June HUH ; Jinyoung SONG ; I Seok KANG
Yonsei Medical Journal 2015;56(5):1437-1442
PURPOSE: Spontaneous pneumomediastinum (SPM) is a rare entity, with only a few cases reported, especially in adolescents. We aimed to analyze the clinical characteristics of SPM in adolescents and the diagnostic implications of computed tomography (CT) and esophagography therein. MATERIALS AND METHODS: This retrospective descriptive study was conducted as a review of medical records of 416 adolescents (10-18 years of age) with chest pain from March 2005 to June 2013. Information on clinical presentation, methods of diagnosis, hospital stay, and outcomes were collected and analyzed. RESULTS: Among adolescents complaining of chest pain, 11 patients had SPM (11/416, 2.64%). All patients presented with pleuritic chest pain, and 54.5% reported neck pain as the most common associated complaint. Clinical findings were nonspecific, and initial chest X-ray assessment was diagnostic only in three of 11 patients. However, reassessment of chest X-ray revealed diagnostic findings of SPM in five of the remaining eight patients. CT was diagnostic in all patients, while esophagography and echocardiogram were uninformative. Symptomatic improvement was noted within 2.45+/-1.2 hours (range, 0.5 to 4) after supportive care; mean hospital stay was 4.54+/-0.99 days (range, 2 to 6). No recurrence was observed. CONCLUSION: SPM is a rare disease that should be considered in adolescent patients with pleuritic chest pain. Careful reading of initial chest X-rays is important to avoiding further unnecessary investigations. SPM is self-limited and treatment is supportive; nevertheless, if there are no indications of esophageal rupture, urgent esophagography is not recommended.
Adolescent
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Analgesics/*therapeutic use
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Chest Pain/diagnosis/*etiology
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Child
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Female
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Follow-Up Studies
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Humans
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Length of Stay
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Male
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Mediastinal Emphysema/complications/*diagnosis/*therapy
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Medical Records
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*Oxygen Inhalation Therapy
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Rare Diseases
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Retrospective Studies
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Risk Factors
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Tomography, X-Ray Computed
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Treatment Outcome