1.Mesothelial Cyst of the Middle and Anterior-Superior Mediastinum: One Case Report.
Sun Ho JEON ; Jung Ho KANG ; Heng Ok JEE ; Young Hak KIM ; Won Sang JUNG ; Hyuck KIM ; Moon Hyang PARK ; Jung Kook SUH ; Seok Choi JEON
The Korean Journal of Thoracic and Cardiovascular Surgery 1998;31(10):1017-1021
Mesothelial cysts have many other names, such as pericardial celomic cyst, pleura-diaphragmatic cyst, simple cyst of the mediastinum, springwater cyst, serosal cyst, etc. (Petereit 1972, Drash 1950). Most mesothelial cysts are believed to originate from malformations of the pericardium, but some, like the one in this case, are believed to result from a pleural malformation. (Ochsner 1966, Lambert 1940). Mesothelial cysts are extremely rare and can be confirmed histologically by special stains. A 64 year old woman was admitted due to a painless bulging mass in her right neck. The operation was performed with the initial diagnosis of cystic lymphangioma confirmed by computer tomography and total excision was possible. The diagnosis of mesothelial cyst of the mediastinum was confirmed by histologic examinations (stainings) and the patient was discharged from the hospital without any significant complications.
Coloring Agents
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Diagnosis
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Female
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Humans
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Lymphangioma, Cystic
;
Mediastinal Cyst
;
Mediastinal Neoplasms
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Mediastinum*
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Middle Aged
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Neck
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Pericardium
2.Mediastinal Lymphangioma in Adults: Three Case Reports.
Kyung Chan KIM ; Won Jung KOH ; O Jung KWON ; Byoung Hoon LEE ; Jung Hye HWANG ; Eun Hae KANG ; Gee Young SUH ; Man Pyo CHUNG ; Hojoong KIM ; Joungho HAN ; Young Hyeh KO ; Jhingook KIM ; Tae Sung KIM ; Kyung Soo LEE
Tuberculosis and Respiratory Diseases 2003;55(3):303-310
BACKGROUND: Lymphangioma of the mediastinum is an uncommon benign tumor of lymphatic origin that is most often seen in children, is very rare in adults and is frequently discovered incidentally on chest x-ray exams. While radiology (CT and MRI) may suggest the diagnosis and allow an assessment of the operative difficulties, the histology of the surgical specimen is required for precise diagnosis. Complete resection is the only treatment; however, in some patients resection was incomplete because of the infiltrating character of these tumors, leading to recurrence. We report three cases of mediastinal lymphangioma with a review of the literature.
Adult*
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Child
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Diagnosis
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Humans
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Lymphangioma*
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Mediastinal Neoplasms
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Mediastinum
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Recurrence
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Thorax
3.The Importance of the Simple Chest X-ray Tend to Make Careless Interpretation: with a Case of Mediastinal Tumor.
Eun Young KIM ; Ju Eun LIM ; Byung Hoon PARK ; Jin Young YOON ; Ji Ye JUNG ; Ji Young SON ; Kyung Jong LEE ; Yoe Wun YOON ; Young Ae KANG ; Jin Wook MOON ; Moo Suk PARK ; Young Sam KIM ; Joon CHANG ; Sung Kwan SHIN ; Se Kyu KIM
Tuberculosis and Respiratory Diseases 2009;66(6):482-485
The middle mediastinum contains several important organs and pluripotent cells. It is difficult to make a definitive diagnosis in patients with middle mediastinal tumors due to a wide range of diseases. The likelihood of malignancy is influenced primarily by the following factors: patient age, size, tumor location, and the presence or absence of symptoms. We describe a case of a middle mediastinal tumor, which was suspected on chest x-ray; chest computed tomography revealed the eccentric mass of distal esophagus. This case emphasizes the diagnostic importance of the chest x-ray to the physicians. The possible differential diagnoses are reviewed.
Diagnosis, Differential
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Esophagus
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Humans
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Leiomyoma
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Mediastinal Neoplasms
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Mediastinum
;
Thorax
4.Rapidly Grown Huge Mediastinal Benign Teratoma: one case report.
Sung Woo JO ; Hyun Geun JEE ; Hyun Sung AHN ; Eun Sook NAM
The Korean Journal of Thoracic and Cardiovascular Surgery 2000;33(6):521-524
The benign teratoma is usually slow growing tumor, but we expirienced a case of primary huge mediastinal benign teratoma that had grown very rapidly, maximally during 3 years. The 14-year-old female patient was admitted to our hospital because of abnormal chest X-ray that showed 10x10cm sized well definded mass with multiple calcificactions. but the mass was not present in chest X-ray perfomed on 3 years prior to admission. Under the diagnosis of teratoma, complete surgical resection was done by the left thoracotomy. The result of pathology was benign teratoma.
Adolescent
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Diagnosis
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Female
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Humans
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Mediastinal Neoplasms
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Pathology
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Teratoma*
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Thoracotomy
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Thorax
5.The diagnostic value of mediastinoscopy and its application in staging for lung cancer.
Xin WANG ; Zhifan HUANG ; Tiehua RONG ; Qiuliang WU ; Xiaoman LIANG ; Mingtian YANG ; Canguang CENG ; Hao LONG ; Peng LIN ; Jianhua FU
Chinese Journal of Oncology 2002;24(1):74-76
OBJECTIVETo evaluate the value of mediastinoscopy in diagnosing unknown mediastinal disease and staging of lung cancers.
METHODSFrom October 2000 to August 2001, 41 patients were examined by cervical mediastinoscopy with or without anterior mediastinotomy for diagnostic and staging purposes. Of these 41 patients, 12 were for diagnosis of unknown mediastinal disease, 3 for diagnosis and staging of pulmonary nodule or mass clinically suspected to be malignancy and 26 for the staging of lung cancer.
RESULTSTen of 12 patients with unknown mediastinal disease were diagnosed pathologically as thymoma in 1, metastatic lesion from lung cancer in 1, metastatic thyroid carcinoma in 1, lymph node hyperplasia in 1, teratoma in 1, sarcoidosis in 1, inflammatory pseudotumor in 1 and tuberculosis in 3, giving a diagnostic rate of 83.3%. Of three patients with suspected malignancy, one was diagnosed as tuberculosis by cervical mediastinoscopy and the other two as lymphoma and pulmonary inflammatory pseudotumor by thoracoscopy and thoracotomy. The sensitivity and specificity of mediastinoscopy for the staging of mediastinal nodes in 26 lung cancers were 87.5% and 100%. Only one wound infection but no other major complication was found.
CONCLUSIONMediastinoscopy is a safe procedure which can accurately provide information on diagnosis and staging.
Adult ; Aged ; Female ; Humans ; Lung Neoplasms ; diagnosis ; Male ; Mediastinal Neoplasms ; diagnosis ; Mediastinoscopy ; Middle Aged ; Neoplasm Staging
6.Mediastinal lymphoma in a young Turkish Angora cat.
Kyoung Won SEO ; Ul Soo CHOI ; Bo Kyoung BAE ; Mi Sun PARK ; Cheol Yong HWANG ; Dae Yong KIM ; Hwa Young YOUN
Journal of Veterinary Science 2006;7(2):199-201
An 8-month old intact male Turkish Angora cat was referred to the Veterinary Medical Teaching Hospital (VMTH), Seoul National University, for an evaluation of anorexia and severe dyspnea. The thoracic radiographs revealed significant pleural effusion. A cytology evaluation of the pleural fluid strongly suggested a lymphoma containing variable sized lymphocytes with frequent mitotic figures and prominent nucleoli. The feline leukemia virus and feline immunodeficiency virus tests were negative. The cat was euthanized at his owner's request and a necropsy was performed. A mass was detected on the mediastinum and lung lobes. A histopathology evaluation confirmed the mass to be a lymphoma. Immunohistochemistry revealed the mass to be CD3 positive. In conclusion, the cat was diagnosed as a T-cell mediastinal lymphoma.
Animals
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Cat Diseases/*diagnosis/pathology
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Cats
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Lymphoma/diagnosis/pathology/*veterinary
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Male
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Mediastinal Neoplasms/diagnosis/pathology/*veterinary
7.Primary mediastinal choriocarcinoma: a difficult and complicated case study.
Yuan-Dong DUAN ; Jing PENG ; Fei YIN
Chinese Journal of Contemporary Pediatrics 2009;11(7):517-520
Primary mediastinal choriocarcinoma is a very rare malignant tumor unrelated to pregnancy. Here a case of primary mediastinal choriocarcinoma was reported. The patient was a 13-year-old boy. He presented with shortness of breath, chest pain, fever, irritable cough and weight loss. The imaging examination showed a huge space-occupying lesion at the right edge of mediastinum. The autopsy results showed right lung and mediastinal choriocarcinoma cell carcinoma. After the introduction of the case, this paper reviewed the clinical characteristics, diagnosis and treatment of primary mediastinal choriocarcinoma.
Adolescent
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Choriocarcinoma, Non-gestational
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diagnosis
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pathology
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therapy
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Diagnosis, Differential
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Humans
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Male
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Mediastinal Neoplasms
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diagnosis
;
pathology
;
therapy
9.Mucoepidermoid Carcinoma of the Thymus: A Case Report.
Gang Deuk KIM ; Hye Won KIM ; Jung Taek OH ; Hyang Jeong JO ; Seon Kwan JUHNG
Journal of Korean Medical Science 2004;19(4):601-603
Mucoepidermoid carcinoma of the thymus is an extremely rare malignant mediastinal neoplasm, and to our knowledge, only 13 cases have been reported. We report a case of mucoepidermoid carcinoma of the thymus that was seen in a 53-yr-old man with right chest pain. Chest CT scan showed a huge, cystic mass having a focal solid portion with direct invasion of the adjacent anterior chest wall and pericardium in the anterior mediastinum. Mucoepidermoid carcinoma of the thymus should be included in the differential diagnosis for masses of the anterior mediastinum associated with extensive cystic changes, although the carcinoma is exceedingly rare.
Carcinoma, Mucoepidermoid/*diagnosis/pathology
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Fatal Outcome
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Humans
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Male
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Mediastinal Neoplasms/*diagnosis/pathology
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Middle Aged
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Thymus Neoplasms/*diagnosis/pathology