• Advances in pediatric surgery
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• 제15권1호
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• pp.68-72
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• 2009

Neuroblastoma is the most common extracranial solid tumor in children, and accompanies various clinical symptoms including hypertension. Hypertension is associated with catecholamines secreted from the tumor, and is usually not severe. We report one case of malignant hypertension with cardiac failure in a patient with adrenal neuroblastoma, successfully treated with adrenalectomy. A 3 year-old boy complained of protrusion of the chest wall. Physical examination revealed severe hypertension with cardiac failure. The levels of metabolites of catecholamine were increased in blood (norepinephrine >2000 pg/mL) and urine (norepinephrine 1350.5 ug/day). Abdominal CT showed a 7 cm-sized solid mass arising from the right adrenal gland. After stabilizing the hemodynamics with oral phenoxybenzamine, right adrenalectomy was performed. Pathological diagnosis was a ganglioneuroblastoma. The hypertension and cardiac failure were resolved after tumor removal.

• Journal of Chest Surgery
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• 제24권7호
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• pp.701-711
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• 1991

We experienced 6 cases of primary cardiac tumor, all received operation for removal of tumor. Mean age was 43.8 years-old ranging from 17 years-old to 66 years-old. Five cases were female, one case was male. Five cases were benign, myxoma, all located within left atrium. One case was malignant, angiosarcoma within right atrium. All patient showed cardiac manifestations. One case was in NYHA functional class II, two were in III, three were in IV. Four patients showed constitutional symptoms, but no one showed evidence of embolic phenomenon. All case of myxoma showed cardiomegaly except one malignancy. Only one case was regular sinus rhythm, three were sinus tachycardia 8z two were atrial fibrillation. The most common site of tumor origin was fossa ovalis limbus[four of all]. Two of five myxomas received emergency operation, one patient died postoperatively. Lived four patients showed no evidence of recurrence[mean follow-up, 3,5 years], but one patient has Grade II /IV mitral regurgitation & in OPD follow-up now, One malignant case, 17 years-old cerebral palsy female, was angiosarcoma occupied most of right atrial chamber originated from anterior wall of right atrium, received emergency operation which was removal of mass & reconstruction of right atrium with artificial pericardial patch. This patient died on postoperative 36th day due to persistent LCOS[low cardiac output syndrome] with combined sepsis.

• Journal of Chest Surgery
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• 제18권4호
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• pp.667-672
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• 1985

Primary cardiac tumors are uncommon in all age group. In contrast, tumors metastatic to the heart are significantly more common. On rare occasions, tumor may extend into the heart chamber via inferior vena cava from other parts of the body, such as liver, kidney, and uterus cava. With recent advancement in diagnostic imaging modalities and surgical techniques, cardiac tumors are now potentially curably form of heart disease. The most important factor in diagnosing the tumor is a high index of clinical suspicion. Six patients underwent surgical removal of intracardiac tumor during a 5-year period. The mean age of the 4 women and two men was 40 years [range 23 to 60]. All patients were operated on in the last five years of the studied period. All patients had symptoms varying in duration from 1 month to 4 years [average 13 months]. 2-Dimensional echocardiography contributed most to preoperative diagnosis, confirming presence of an intracardiac tumor in all examined patients. Of the six intracardiac tumor, 5 were myxomas [4 left atrial and 1 right ventricular] and one right atrial metastasis from hepatocellular carcinoma of the liver. In all cases, tumor masses were successfully excised. One patient expired after the operation on account of low cardiac out-put syndrome. Remained one patient among six, tumor mass extended into RA and RV with a stalk via IVC. On later follow-up study showed cold area on liver scan [hepatocellular ca.], so she was transferred to internal medicine, department for chemotherapy. Follow up results showed no signs of tumor recurrence in 4 myxoma cases.

• 정보처리학회논문지B
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• 제18B권2호
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• pp.57-66
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• 2011

심장 질환을 예방하기 위해서는 정기적인 검진을 통해 심장 기능을 분석하고 관찰하는 것이 중요하다. 정기적인 검진에서 심장 기능은 심장을 촬영한 후에 관측자가 이를 수작업을 통하여 처리하여 혈류량과 심박구출률 등을 분석함으로서 이루어지나, 시간도 오래 걸리며 관측자에 따른 변이성이 문제가 된다. 본 논문에서는 심장 단축 자기공명영상에서 좌심실 영역을 분할하는 자동화된 알고리즘을 제안한다. 코일 위치에 따른 왜곡을 보정하고, K-평균 클러스터링 기법을 이용하여 좌심실 내부를 분할한다. 영상의 왜곡 및 잡음에 의하여 발생하는 분할 오류는 그래프 탐색 기법을 적용하여 수정하였다. 제안하는 알고리즘의 성능을 평가하기 위하여 38명의 지원자 그룹에 대하여 혈류량과 심박구출률을 계산하였고, 전문가에 의한 수동윤곽검출 결과와 GE MASS 소프트웨어와 비교하였다. 결과에 따르면 제안한 알고리즘의 수동윤곽검출과 혈류량의 차이는 평균적으로 이완기에 6.2mL${\pm}$5.6 및 수축기에 2.9mL${\pm}$3.0, 심박구출률의 차이는 2.1%${\pm}$1.5로 높은 정확성을 보였다. 특히 제안한 알고리즘은 기존 알고리즘에서 발생하던 사용자 간섭률을 최소화하여 자동화 성능을 향상하였다.

• 정보처리학회논문지B
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• 제15B권6호
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• pp.507-516
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• 2008

최근 연구 결과에 따르면 여러가지 질환 중에 심장 질환으로 인한 사망률이 가장 높은 것으로 나타났다. 임상 실습에서 심장 기능은 좌심실을 수동윤곽검출하여 혈류량이나 심박구출률을 계산하여 분석하지만, 많은 시간과 비용을 필요로 한다. 본 연구에서는 심장을 촬영한 단축 자기공명영상을 사용하여 자동 좌심실 분할 알고리즘을 제안한다. 코일 위치에 따른 왜곡을 보상하고, 에지 정보를 검출하고 특성에 따라 분류한후에, 영역 확장 기법을 사용하여 좌심실을 분할하였다. 또한 부분 복셀소(voxel)의 영향을 고려하였다. 코넬대학교 IRB의 승인하에 38 명의 심장 자기공명영상을 사용하여 제안한 알고리즘을 수동윤곽검출 및 GE MASS 소프트웨어와 비교하였다. 심장의 이완기와 수축기에 혈류량은 부분 복셀소 영향을 고려하지 않을 경우 각각 $3.3mL{\pm}5.8$(표준편차)와 $3.2mL{\pm}4.3$, 부분 복셀소 영향을 고려한 경우 각각 $19.1mL{\pm}8.8$와 $10.3mL{\pm}6.1$의 정확도를 보였다. 심박구출률은 부분 복셀소 영향을 고려하지 않은 경우와 고려한 경우에 대해서 각각 $-1.3%{\pm}2.6$ 와 $-2.1%{\pm}2.4$의 정확도를 보였다. 이를 통해 제안한 알고리즘이 정확하고 정기적인 임상 실습에 유용함을 확인할 수 있다.

• Investigative Magnetic Resonance Imaging
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• 제15권2호
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• pp.165-169
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• 2011

심장점액종은 심장의 가장 흔한 양성 종양이다. 하지만 국소전이와 원격전이의 증례들이 낮은 빈도로 보고되어 있다. 뇌경색을 주소로 내원한 49세 여자 환자의 심장초음파에서 심장 점액종이 발견되었으며 수술로 절제 1년 후에 구음장애가 발생하여 촬영한 자기공명영상에서 여러개의 조영증강이 되는 출혈성뇌전이 병변들이 관찰되었다. 방사선치료 후 추적 자기공명영상에서 병변의 크기들이 작아지는 것을 확인할 수 있었다. 양성 종양이지만 심장 점액종은 드물게 지연되어 전이를 보일 수 있다. 저자들은 심장 점액종을 수술로 완전히 절제 후 지연되어 나타난 뇌전이를 경험하여 증례 및 문헌고찰을 하는 바이다.

• Journal of Chest Surgery
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• 제47권2호
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• pp.141-144
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• 2014

We present a case of a 55-year-old woman who complained of chest pain at rest. A mass was detected adjacent to her left atrium. The mass was completely excised, and a pathologic examination revealed it to be a schwannoma. Schwannomas are tumors that originate in the nerve sheath and are rarely detected in the heart. Here, we describe a rare case of primary schwannoma of the left atrium.

• Journal of Chest Surgery
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• 제27권4호
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• pp.310-312
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• 1994

Primary cardiac lipoma is an extremely rare condition. We reports a case of primary lipoma located mainly in the right atrium of the heart in a 58-year-old male patient. The initial presenting symptoms were dyspnea followed by rapidly progress!ve congestive heart failure. Echocardiogram revealed huge mass on right atrium with stalk arising from septum. Under cardiopulmonary bypass the mass was removed and revealed characteristic findings of lipoma on microscope. The patient was recovered without any problem. We would like to describe this case of rare tumor with the review of literatures.

• Korean Journal of Radiology
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• 제22권7호
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• pp.1054-1065
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• 2021

Objective: We implemented a novel resectable myocardial model for mock myectomy using a hybrid method of three-dimensional (3D) printing and silicone molding for patients with apical hypertrophic cardiomyopathy (ApHCM). Materials and Methods: From January 2019 through May 2020, 3D models from three patients with ApHCM were generated using the end-diastolic cardiac CT phase image. After computer-aided designing of measures to prevent structural deformation during silicone injection into molding, 3D printing was performed to reproduce anatomic details and molds for the left ventricular (LV) myocardial mass. We compared the myocardial thickness of each cardiac segment and the LV myocardial mass and cavity volumes between the myocardial model images and cardiac CT images. The surgeon performed mock surgery, and we compared the volume and weight of the resected silicone and myocardium. Results: During the mock surgery, the surgeon could determine an ideal site for the incision and the optimal extent of myocardial resection. The mean differences in the measured myocardial thickness of the model (0.3, 1.0, 6.9, and 7.3 mm in the basal, midventricular, apical segments, and apex, respectively) and volume of the LV myocardial mass and chamber (36.9 mL and 14.8 mL, 2.9 mL and -9.4 mL, and 6.0 mL and -3.0 mL in basal, mid-ventricular and apical segments, respectively) were consistent with cardiac CT. The volume and weight of the resected silicone were similar to those of the resected myocardium (6 mL [6.2 g] of silicone and 5 mL [5.3 g] of the myocardium in patient 2; 12 mL [12.5 g] of silicone and 11.2 mL [11.8 g] of the myocardium in patient 3). Conclusion: Our 3D model created using hybrid 3D printing and silicone molding may be useful for determining the extent of surgery and planning surgery guided by a rehearsal platform for ApHCM.

• Journal of Chest Surgery
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• 제40권12호
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• pp.859-862
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• 2007

심장 판막엽에 발생하는 혈관종은 극히 드문 질환으로 최근까지 문헌에 보고된 것은 총 5례가 전부이며 아직까지 국내문헌에는 보고된 바가 없다. 건강하던 46세 여자가 갑자기 발생한 좌측 안면마비와 수부 감각이상을 주소로 내원하였다. 신경학적 검사에서는 이상 소견이 없었으며 심장초음파에서 승모판막 전엽에 위치한 종괴가 발견되어 종괴를 포함한 승모판막 전엽의 일부를 절제한 후 자가심낭을 이용하여 승모판막성형을 시행하였다. 병리조직 검사상 승모판막 전엽에 발생한 혈관종으로 판명되어 문헌고찰과 함께 보고하는 바이다.