ABSTRACT
Tracheal chondromas are very rare benign cartilaginous tumors. We present the first case report, to our knowledge, of a tracheal chondroma in Korea. A 73-year-old male was referred to our hospital for a mass in the left lung. Flexible bronchoscopy was performed to evaluate the lung mass and incidentally found a tracheal mass as well. A biopsy and histological examination of the tracheal mass revealed a chondroma.
Subject(s)
Aged , Humans , Male , Biopsy , Bronchoscopy , Chondroma , Korea , Lung , Lung Neoplasms , Tracheal NeoplasmsABSTRACT
An 85-year-old male visited our hospital because of dyspnea. Chest radiography showed marked cardiomegaly and pneumonic infiltration. Transthoracic echocardiography showed moderate pericardial effusion, which resulted in effusive constrictive pericarditis and severe left ventricular systolic dysfunction. During the hospital course, the patient developed cardiogenic shock and was treated with an inotropic agent and intra-aortic balloon pump. The patient's vital signs were stabilized after pericardiocentesis and drainage. A yellowish purulent pericardial effusion was drained and Streptococcus pneumoniae was isolated. Bacterial purulent pericarditis was not uncommon before the antibiotics era, but it is extremely rare nowadays. Here, we report a case of purulent bacterial pericarditis presenting with severe left ventricular systolic dysfunction and cardiac tamponade.
Subject(s)
Aged, 80 and over , Humans , Male , Anti-Bacterial Agents , Cardiac Tamponade , Cardiomegaly , Drainage , Dyspnea , Echocardiography , Pericardial Effusion , Pericardiocentesis , Pericarditis , Pericarditis, Constrictive , Shock, Cardiogenic , Streptococcus pneumoniae , Thorax , Ventricular Dysfunction , Vital SignsABSTRACT
A 36-year-old primivida, at 29 weeks of pregnancy with no smoking history, was admitted to the hospital complaining of cough for 3 days. Chest X-rays revealed atelectasis of the right upper lobe, and a transbronchial lung biopsy confirmed primary lung adenocarcinoma. After consulting with obstetricians and neonatologists, we wanted to deliver the child and treat the mother with chemoradiotherapy. But as she was adamantly opposed to treatment until fetal lung maturation was complete, we planned to delay the birth until 34 weeks, deliver the baby by caesarian section, and then treat the mother. However, maternal hypoxia and fetal distress resulted in an emergency delivery at 30 weeks. After delivery, we treated the mother's brain metastases with radiation therapy and systemic cisplatin-pemetrexed, but she deteriorated and expired 95 days after the diagnosis. Lung cancer during pregnancy is a rare disease and raises many medical and ethical issues in deciding the best course of therapy. We describe our clinical approach and review the potentially challenging features of managing a pregnant patient with lung cancer.
Subject(s)
Adult , Child , Humans , Pregnancy , Adenocarcinoma , Hypoxia , Biopsy , Brain , Chemoradiotherapy , Cough , Emergencies , Fetal Distress , Lung , Lung Neoplasms , Mothers , Neoplasm Metastasis , Parturition , Pulmonary Atelectasis , Rare Diseases , Smoke , Smoking , ThoraxABSTRACT
An 85-year-old male visited our hospital because of dyspnea. Chest radiography showed marked cardiomegaly and pneumonic infiltration. Transthoracic echocardiography showed moderate pericardial effusion, which resulted in effusive constrictive pericarditis and severe left ventricular systolic dysfunction. During the hospital course, the patient developed cardiogenic shock and was treated with an inotropic agent and intra-aortic balloon pump. The patient's vital signs were stabilized after pericardiocentesis and drainage. A yellowish purulent pericardial effusion was drained and Streptococcus pneumoniae was isolated. Bacterial purulent pericarditis was not uncommon before the antibiotics era, but it is extremely rare nowadays. Here, we report a case of purulent bacterial pericarditis presenting with severe left ventricular systolic dysfunction and cardiac tamponade.
Subject(s)
Aged, 80 and over , Humans , Male , Anti-Bacterial Agents , Cardiac Tamponade , Cardiomegaly , Drainage , Dyspnea , Echocardiography , Pericardial Effusion , Pericardiocentesis , Pericarditis , Pericarditis, Constrictive , Shock, Cardiogenic , Streptococcus pneumoniae , Thorax , Ventricular Dysfunction , Vital SignsABSTRACT
While nontuberculous mycobacterium (NTM) infections are recently on the rise, arthritis caused by NTM is hardly reported in Korea. NTM arthritis has no distinctive clinical characteristics from chronic arthritis. Tuberculosis of the joint specifically produces similar clinical and pathologic presentations to NTM arthritis, so it is not easy to distinguish between them. We report a case of Mycobacterium intracellulare in an arthritis patient after trauma and surgical repair of the injury. At the beginning, the patient was diagnosed as tuberculous tenosynovitis through pathology without microbiologic evidence. The final diagnosis was made after subsequent recurrences for several years. The misdiagnosis and delayed diagnosis led to irreversible joint destruction and functional impairment. NTM infection must be included in the differential diagnosis of chronic arthritis at the outset.
Subject(s)
Humans , Arthritis , Delayed Diagnosis , Diagnosis, Differential , Diagnostic Errors , Joints , Korea , Mycobacterium , Mycobacterium avium Complex , Mycobacterium avium-intracellulare Infection , Nontuberculous Mycobacteria , Recurrence , Tenosynovitis , TuberculosisABSTRACT
External compression of the right ventricle (RV) due to a depressed sternum in patients with pectus excavatum is uncommon. Moreover, mid-RV obstruction-induced cachexia rarely occurs in patients with pectus excavatum. We report a case of cardiac cachexia caused by significant RV compression in a patient with pectus excavatum.
Subject(s)
Humans , Cachexia , Funnel Chest , Heart Ventricles , Sternum , Ventricular Dysfunction, RightABSTRACT
Left ventricular hypertrabeculation/noncompaction (LVHT) is an uncommon type of genetic cardiomyopathy characterized by trabeculations and recesses within the ventricular myocardium. LVHT is associated with diastolic or systolic dysfunction, thromboembolic complications, and arrhythmias, including atrial fibrillation, ventricular arrhythmias, atrioventricular block and Wolff-Parkinson-White syndrome. Herein, we describe a patient who presented with heart failure and wide-complex tachycardia. Echocardiography showed LVHT accompanied with severe mitral regurgitation. The electrophysiologic study revealed a fasciculo-ventricular accessory pathway and atrial flutter (AFL). The AFL was successfully treated with catheter ablation.
Subject(s)
Humans , Arrhythmias, Cardiac , Atrial Fibrillation , Atrial Flutter , Atrioventricular Block , Cardiomyopathies , Catheter Ablation , Echocardiography , Heart Failure , Isolated Noncompaction of the Ventricular Myocardium , Mitral Valve Insufficiency , Myocardium , Pre-Excitation, Mahaim-Type , Tachycardia , Wolff-Parkinson-White SyndromeABSTRACT
A 36-year-old primivida, at 29 weeks of pregnancy with no smoking history, was admitted to the hospital complaining of cough for 3 days. Chest X-rays revealed atelectasis of the right upper lobe, and a transbronchial lung biopsy confirmed primary lung adenocarcinoma. After consulting with obstetricians and neonatologists, we wanted to deliver the child and treat the mother with chemoradiotherapy. But as she was adamantly opposed to treatment until fetal lung maturation was complete, we planned to delay the birth until 34 weeks, deliver the baby by caesarian section, and then treat the mother. However, maternal hypoxia and fetal distress resulted in an emergency delivery at 30 weeks. After delivery, we treated the mother's brain metastases with radiation therapy and systemic cisplatin-pemetrexed, but she deteriorated and expired 95 days after the diagnosis. Lung cancer during pregnancy is a rare disease and raises many medical and ethical issues in deciding the best course of therapy. We describe our clinical approach and review the potentially challenging features of managing a pregnant patient with lung cancer.
Subject(s)
Adult , Child , Humans , Pregnancy , Adenocarcinoma , Hypoxia , Biopsy , Brain , Chemoradiotherapy , Cough , Emergencies , Fetal Distress , Lung , Lung Neoplasms , Mothers , Neoplasm Metastasis , Parturition , Pulmonary Atelectasis , Rare Diseases , Smoke , Smoking , ThoraxABSTRACT
Tracheal chondromas are very rare benign cartilaginous tumors. We present the first case report, to our knowledge, of a tracheal chondroma in Korea. A 73-year-old male was referred to our hospital for a mass in the left lung. Flexible bronchoscopy was performed to evaluate the lung mass and incidentally found a tracheal mass as well. A biopsy and histological examination of the tracheal mass revealed a chondroma.
Subject(s)
Aged , Humans , Male , Biopsy , Bronchoscopy , Chondroma , Korea , Lung , Lung Neoplasms , Tracheal NeoplasmsABSTRACT
A traumatic pulmonary pseudocyst is a rare complication of blunt thoracic trauma. The clinical symptoms and signs are similar to other respiratory diseases, such as pulmonary tuberculosis. Therefore, a trauma history with the resulting radiologic and clinical findings is important for making a diagnosis. A 26-year-old male was admitted to our hospital due to cough for 3 days. The chest x-ray revealed diffuse infiltrations and a cavitary lesion at the left lung. His left chest had hit a tree as a result of motorcycle accident one day before admission. Initially, it was assumed that his symptoms and chest X-ray might be due to a tuberculosis infection. However, bronchoscopy revealed old blood clots at both lungs, particularly in the left lower lobe bronchus. A transbronchial lung biopsy showed alveolar hemorrhage. A traumatic pulmonary pseudocyst was diagnosed from his trauma history and these findings. Computed tomography of the chest performed 4 months later showed regression of the cavitary lesion.