• Journal of Chest Surgery
• /
• 제9권1호
• /
• pp.90-93
• /
• 1976

Pulmonary hamartoma is often incidental, asymptomatic finding on routine chest roentgenogram. It has been considered a congenital malformation. Since the original description by Albrecht in 1908, it has been classified into two types, a small, fibrocartilaginous mass in adults, and a cystic lobar mass in infants. We experienced two cases of pulmonary hamartoma which proved to be the adult form of hamartoma. One was located in left upper lobe of a 58 year old male patient, the other was located in the perihilar region of the right middle lobe of a 38 year old male patient. The former case was treated by wedge resection: the latter by right middle lobectomy and the postoperative courses of both cases were very good and without complication.

• Journal of Chest Surgery
• /
• 제17권3호
• /
• pp.470-474
• /
• 1984

33-year old female was admitted chest surgery department for evaluation of mild chest pain. Chest plain film showed right anterior mediastinal mass and small metastatic daughter mass ipsilateral side. Exploratory thoracotomy was performed 24th Aug. 83 revealed that small nodular parenchymal mass at right middle lobe and large cystic mass at anterior mediastinum which was connected with anterior mediastinal fat. Histological examination confirmed diagnosis as pulmonary hamartoma and thymic cyst individually. We successfully treated these two masses by wedge resection and excision. Although postoperative course was uneventful, the cause and associated relationship between two tumor origin were obscure.

• 한국정보처리학회:학술대회논문집
• /
• 한국정보처리학회 2014년도 춘계학술발표대회
• /
• pp.992-994
• /
• 2014

Hemispheric asymmetry in prefrontal activation have been proposed in two decades ago, as measured by electroencephalographic (EEG) power in the theta band (4-8Hz), is related to reactivity to affectively pleasure audio stimuli. In this study, we designed an emotional audio stimulus experiment in order to verify frontal EEG asymmetry by analyzing ERSP results. Thirty healthy college students volunteered the stimulus experiment with the standard IADS affective sounds. These affective sound clips are classified in three emotion states, happy, neutral and fear. ERSP image results revealed that there are the stronger responses of high arousal (fear and happy) in the left prefrontal lobe, while the stronger responses of low arousal (neutral) in the right pre-frontal lobe. However, the high pleasure emotions (happy) can elicit greater relative right EEG activity, while the low and middle pleasure emotions (fear and neutral) can elicit the greater relative left EEG activity. Additionally, the most response differences of theta band have been found out in the medial frontal lobe, which is proved as the frontal midline theta.

• Tuberculosis and Respiratory Diseases
• /
• 제62권3호
• /
• pp.192-196
• /
• 2007

배 경: 우중엽증후군은 반복적이고 만성적인 우중엽의 허탈을 나타내는 질환으로 그 원인은 매우 다양하다. 최근 국내에서 우중엽증후군의 원인에 대한 발표는 부족한 실정이어서 저자들은 최근 수년간 지역 3차 병원에서 경험한 우중엽증후군의 원인과 임상적 특징을 알아보고자 하였다. 방 법: 2003년 1월부터 2006년 7월까지 경상대학교 병원에 내원하여 흉부 단순촬영 또는 전산화 단층촬영에서 우중엽증후군이 의심되어 기관지내시경 검사를 시행한 88명의 환자(남:여=22:64, 평균연령: $67.2{\pm}10.3$)를 대상으로 그 원인과 임상적 특징을 후향적으로 조사하였다. 결 과: 1) 여자가 64예(72.7%)로 남자보다 많았고 연령별 빈도에서 65세 이상의 고령환자가 58예로 65.9%를 차지하였다. 2) 임상 증상은 기침이 30예(34.1%)로 가장 흔하게 나타났고, 호흡곤란 21예(23.9%), 객담 15예(17.0%), 객혈 11예(12.5%), 흉부통증과 전신 쇠약감이 각각 5예(5.7%)에서 나타났으며, 증상이 없이 우연히 발견된 경우가 8예(9.1%)였다. 3) 흉부 방사선 촬영에서는 무기폐 49예(55.7%), 폐경화 43예(48.9%), 종괴 4예(4.5%) 소견을 보였다. 4) 기관지내시경 검사 소견에서 충혈을 동반한 점막 부종 38예(43.2%), 탄분증을 동반한 점막 부종 16예(18.2%), 점액 매복(mucus impaction) 13예(14.8%), 섬유성 협착 10예(11.4%), 종괴 8예(9.1%), 삼출성 조직 괴사 4예(4.5%), 외인성 압박에 의한 협착 2예(2.3%), 정상 12예(13.6%)로 나타났다. 5) 원인 질환은 결핵이 23예(26.1%, 기관지 결핵 22예, 폐결핵 1예)로 가장 많았고, 염증성 변화에 의한 양성 협착 22예(25%), 탄분섬유화증 13예(14.8%), 폐렴 11예(12.5%), 폐암 10예(11.4%), 점액 매복 3예(3.4%), 기관지 확장증 2예(2.3%), 특별한 이상이 발견되지 않은 경우가 7예(8.0%)이었다. 결 론: 본 연구에서 우중엽증후군은 65세 이상의 환자에서 흔하게 관찰되었으며, 원인은 대부분 양성질환이었고, 그 중 기관지 결핵이 가장 흔한 원인이었다.

• Tuberculosis and Respiratory Diseases
• /
• 제72권6호
• /
• pp.501-506
• /
• 2012

Congenital cystic adenomatoid malformation (CCAM) is an uncommon, nonhereditary anomaly caused by arrest of lung. Patients with CCAM may present with respiratory distress as newborns, or may remain asymptomatic until later in life. CCAM type I is rarely found in association with bronchial atresia (BA) in adults; we present such a case. Case: A 54-year-old female presented with chronic cough and blood-tinged sputum. Physical examination and laboratory tests were unremarkable. Chest radiographs and a CT scan of the chest showed multiple large air-filled cysts consistent with a CCAM in the right lower lobe, and an oval-shaped opacity in the distal right middle lobal bronchus. Based on the radiologic findings, right middle lobectomy and a medial basal segmentectomy of the right lower lobe were performed via a thoracotomy. These lesions were consistent with Stocker's Type I CCAM and BA in the different lobes.

• Journal of Chest Surgery
• /
• 제32권4호
• /
• pp.408-412
• /
• 1999

1956년 Liebow and Hubbell 의해 폐에 생긴 경화성 혈관종이 처음 보고된 이후 단독결절에 대해서는 여러 차례 발표된 예가 있었으나 다발성으로 경 \ulcorner\ulcorner혈관종이 생긴 예는 극히 드물다. 이 종양의 조직생성 원인은 아직 논란의 여지가 있으며 그 기원에 대한 여러가설이 있는 것으로 알려져 있다. 환자는 57세 여자 주부였으며 3개의 다른 결절이 발견되였고 하나는 우중엽에 또 다른 하나는 좌상엽의 폐첨후 분절에 나머지는 좌하엽의 상분엽에 위치하였다. 환자의 유일한 증상은 마른기침 이였다. 수술은 좌상엽의 폐첨후 분절 절제술 및 좌하엽의 상분절 쐐기 절제술의 방법으로 시행하였다. 수술후 경과는 큰 문제가 없었으며 환자는 술후 15일에 퇴원하였다.

• Journal of Yeungnam Medical Science
• /
• 제7권2호
• /
• pp.141-149
• /
• 1990

The authors conducted a clinical observation of 55 cases of solitary pulmonary nodules at Yeungnam University Hospital from June 1986 to October 1990, and the following results were obtained : 1. The age distribution was ranged from 18 to 77 years, and the male-to-female ratio was 1.8:1. 2. Among 55 cases of nodules, 28 cases were benign and 27 cases were malignant nodules, and of malignant nodules, the primary lung cancer was 23 cases and of benign nodules, 18 cases were tuberculoma. 3. 23 cases (41.8%) was asymptomatic and the other 32 cases were symptomatic; chest pain 12 cases, hemoptysis; 8 cases, cough; 8 cases and dyspnea; 4 cases. 4. The non-smoker-to-smoker ratio was 1:1.04, but among 23 smoker over 20 pack years, 14 cases were malignant nodules. 5. According to nodular size, there is no striking differences between benign and malignant nodules except 3-4cm sized nodules. 6. The lobar distribution of nodules, 35 cases were in the right lung (upper lobe; 14 cases, middle lobe; 11 cases, and lower lobe; 10 cases) and 20 cases were in the left lung(upper lobe; 9 cases, lower lobe; 11 cases), and the malignant nodules were most commonly observed in the right upper lung.

• 한국간담췌외과학회지
• /
• 제28권3호
• /
• pp.388-392
• /
• 2024

In liver transplantation, the primary concern is to ensure an adequate future liver remnant (FLR) volume for the donor, while selecting a graft of sufficient size for the recipient. The living donor-resection and partial liver segment 2-3 transplantation with delayed total hepatectomy (LD-RAPID) procedure offers a potential solution to expand the donor pool for living donor liver transplantation (LDLT). We report the first case involving a cirrhotic patient with autoimmune hepatitis and hepatocellular carcinoma, who underwent left lobe LDLT using the LD-RAPID procedure. The living liver donor (LLD) underwent a laparoscopic left hepatectomy, including middle hepatic vein. The resection on the recipient side was an extended left hepatectomy, including the middle hepatic vein orifice and caudate lobe. At postoperative day 7, a computed tomography scan showed hypertrophy of the left graft from 320 g to 465 mL (i.e., a 45.3% increase in graft volume body weight ratio from 0.60% to 0.77%). After a 7-day interval, the diseased right lobe was removed in the second stage surgery. The LD-RAPID procedure using left lobe graft allows for the use of a small liver graft or small FLR volume in LLD in LDLT, which expands the donor pool to minimize the risk to LLD by enabling the donation of a smaller liver portion.

• Journal of Korean Neurosurgical Society
• /
• 제41권2호
• /
• pp.120-122
• /
• 2007

Meningiomas arise from meningothelial cells that line the arachnoid membrane. So most meningiomas are dural-based lesion. But meningiomas without dural-attachment do occur and are less common. We report our experience of intraparenchymal sylvian fissure menigioma. A 21-year-old female presented with a one-month history of headache that was associated with long-term intermittent partial seizure. CT revealed about $4.5{\times}4.3{\times}5.5cm$ sized calcified mass with enhancement in right temporal lobe. On MR imaging, the lesion was observed in the right temporal lobe that was low-signal intensity on T2WI and iso-signal intensity on T1WI with well enhancement. Operation was performed via right orbitocranial approach. The internal surface of dura was intact. Tumor was totally removed except the capsule of tumor adhered to main trunk of middle cerebral artery. The histopathology showed meningioma, psammomatous type. Intraparenchymal meningioma should be considered in the differential diagnosis of intraaxial lesions in patients of any age group.

• Journal of Chest Surgery
• /
• 제28권4호
• /
• pp.431-436
• /
• 1995

Congenital esophago-bronchial fistula without atresia is very rare and usually demonstrate more insidious clinical effects, and patients may reach adult life before the diagnosis. We had been experienced a typical case of esophago-bronchial fistula without atresia and document the case. A 42-year-old women was admitted to our hospital due to frequent choking symptom and attacks of pneumonia, and patient status was in chronic pulmonary infection status such as most probably bronchiectatic state of right middle & lower lobe including significant destructive changes. We had confirmed esophago-bronchial fistula without atresia with esophagoscopy, esophagogram, and chest CT, and performed esophago-bronchial fistulectomy and right middle & lower lobectomy. Its belongs to type II of Braimbridge`s classification for congenital esophago-bronchial fistula. Postoperation course was smooth and uneventful.