• 제목/요약/키워드: Cardiovascular imaging

검색결과 361건 처리시간 0.021초

요추 압박 골절의 골 시멘트를 이용한 척추성형술 치료 후 발생한 폐동맥 시멘트 혈전증: 증례보고 (Pulmonary Bone Cement Embolism Following Percutaneous Vertebroplasty)

  • 차용한
    • Journal of Trauma and Injury
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    • 제28권3호
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    • pp.202-205
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    • 2015
  • Purpose: Pulmonary cement embolization after vertebroplasty is a well-known complication. The reported incidence of pulmonary cement emboli after vertebroplasty ranges frome 2.1% to 26% with much of this variation resulting from which radiographic technique is used to detect embolization. Onset and severity of symptoms are variable. Case description: We present the case of a 83-year-old women who underwent fourth lumbar vertebroplasty and subsequently had dyspnea several days later. Posteroanterior chest radiography showed multiple linear densities. Computed tomography of thorax revealed also multiple bilateral, linear hyperdensities within the lobar pulmonary artery branches are detected in axial and coronal views. Literature Reviews: Operative management of vertebral compression fractures has included percutaneous vetebroplasty for the past 25 years. Symptoms of pulmonary cement embolism can occur during procedure, but more commonly begin days to weeks, even months, after vertebroplsty. Most cases of pulmonary cement emboli with cardiovascular and pulmonary complications are treated nonoperatively with anticoagulation. Endovascular removal of large cement emboli from the pulmonary arteries is not without risk and sometimes requires open surgery for complete removal of cement pieces. Conclusion: Pulmonary cement embolism is a potentially serious complication of vertebroplasty. If a patient has chest pain or respiratory difficulty after the procedure, chest radiography and possibly advanced chest imaging studies should be performed immediately.

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대동맥-상대정맥루를 동반한 A형 대동맥 해리증 수술 치험 -1례보고- (Type A Aortic Dissection with Aortocaval Fistula -Report of 1 case-)

  • 김흥수;양승인;정성운;김종원;이형렬
    • Journal of Chest Surgery
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    • 제35권8호
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    • pp.599-604
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    • 2002
  • 급성 혹은 만성 대동맥 해리증은 파열을 일으킬 수 있는데 이는 사망의 주요 원인이 된다. 상행대동맥의 해리성 동맥류(Stanford A형 대동맥 해리증)는 극히 드물게 상대정맥으로 파열되어 대동백-상대정맥루를 형성할 수 있는데 대동백-하대정맥루는 복부 대동맥류 환자에서 이따금씩 보고되어 왔다. 최근 상대정맥증후군의 증상을 가진 67세 남자환자에서 CT, MR angiography, 동맥촬영 등 방사선학적 검사결과 Stanford A형 대동맥 해리증 및 대동맥-상대정맥루가 진단되었다. 해리된 동맥류는 절제 후 인조혈관으로 치환되었고 대동맥-상대정맥루는 초저온 순환정지 상태에서 교정되었다. 이에 대해 상세하게 기술하는 바이다.

말초동맥에 발생한 가성동맥류의 외과적 치료 -치험 6례- (Pseudoaneurysms of Peripheral Arteries - A Report of 6 Cases-)

  • 류완준;조창욱
    • Journal of Chest Surgery
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    • 제29권8호
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    • pp.927-930
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    • 1996
  • 인제의대 서울백병원에서는 1986년부터 1994년까지 말초동맥에 발생한가성동맥류환자 6례를 수술 치험하였다. 발생원인은 자상의 일차 봉합술 후 3례, 혈관에 도관삽입 후 2례, 골절상 후 고정 핀을 제거하기 위한 수술 후 1례였다. 발생부위는심부 대퇴동맥 2례, 총대퇴동맥 2례, 쇄골하동맥과 액와동맥에 각각 1례였다. 증상은 박동성 종괴가 4례에서 촉지되었고, 청진시 잡음은 3례, 동통과 종창이 2례, 압통이 1례에서 있었다. 이 중 5례에서 수술을 시행하였다. 수술은 2례에서 심부 대퇴동맥을 결찰하여 가성동맥류를 제거하였다. 단순 가성동맥류의 절제, 요피정맥을 연결하여 성형술, 복재정맥의 첩제를 이용한 성형술을 각각 1례에서 시행하여 가성동맥류를 제거하였다. 1례는 자연 치유되었다.

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신생아에서 발생한 심장 섬유종의 외과적 치료 -1례 보고- (Successful Removal of a Cardiac Fibroma in Infant)

  • 김시호;조범구;홍유선
    • Journal of Chest Surgery
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    • 제28권5호
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    • pp.491-494
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    • 1995
  • A fibroma arising in the right ventricle outflow tract of a 14 month-old infant was successfully removed. The patient was first seen because of shortness of breath and tachycardia. Pertinent clinical and laboratory findings included a grade II/VI systolic murmur, blood pressure of 120/60 mmHg, slight cardiomegaly on chest X-ray, a mass obstructing the outflow tract of the right ventricle on echocardiography and magnetic resonance imaging. On october 30,1992, under cardiopulmonary bypass, a 4cm x 3cm x 3cm tumor was resected from the right ventricular outflow tract, together with a portion of the ventricular wall. Histologically, it was diagnosis as a fibroma. The patient was sent home on the 6th postoperative day following an uneventful recovery form the operation. Although cardiac fibroma is the second most common cardiac tumor in infancy and childhood, it is usually found in the left ventricle and one arising in the right ventricle is considered rare. Although it is a benign tumor, it could produce a severe cardiac dysfunction and even sudden death, depending on its size and location. With the advance in diagnostic techniques and operative management, there is a renewed interest in the early detection and operative removal of these tumors. The case herein presented is the first such case successfully managed and reported in the Korean literature.

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좌측 상 배부 통증으로 발현된 폐혈전색전증의 증례 -증례 보고- (Pulmonary Thromboembolism Presenting with Upper Thoracic Back Pain -A case report-)

  • 이지영;최진환;최창훈
    • The Korean Journal of Pain
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    • 제19권1호
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    • pp.119-122
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    • 2006
  • Upper thoracic back pain can be musculoskeletal in origin or it could be visceral referred pain, which may be indicative of a serious medical condition. We experienced a case of a 55-years-old female patient who complained of upper thoracic back pain for 1 month, which started 10 days after a traffic accident. She described the pain as being a dull, constant nagging sensation with an intensity of 4/10 on the visual analogue scale. Her pain did not subside after trigger point injection of the rhomboid and trapezius muscles. She reported intermittent palpitation, which indicated that the cardiovascular or pulmonary systems were involved. She was diagnosed with pulmonary thromboembolism by the imaging studies. Refractory upper thoracic back pain should be investigated to rule out this treatable, but potentially fatal condition.

폐동맥 판막 기원의 폐동맥 육종에 의한 우심실 유출로 폐쇄 - 1예 보고 - (RVOTO Caused by Pulmonary Artery Sarcoma Originating from Pulmonary Valve - One case report -)

  • 김대현;이인호;윤호철;김수철;김범식;조규석;박주철
    • Journal of Chest Surgery
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    • 제37권2호
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    • pp.173-175
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    • 2004
  • 원발성 폐동맥 육종, 특히 폐동맥 판막에서 기원한 폐동맥 육종은 극히 드물다. 35세 남자 환자가 노작성 호흡곤란과 전신무력감을 주소로 입원하였다. 흉부 컴퓨터 단층촬영, 흉부 자기공명영상, 심장초음파 검사, 폐동맥 조영술상 주 폐동맥 및 양측 폐동맥의 내강에서 커다란 종괴가 관찰되었다. 폐동맥의 원발성 악성 종양으로 생각하고 심폐순환하에 절제를 시행하였다. 폐동맥 판막의 후엽에서 기원한 것으로 보이는 종괴가 폐동맥 판막의 하부에서부터 주폐동맥 및 양측 폐동맥까지 뻗어 있었고, 폐동맥 내막절제술을 통한 종괴의 절제 및 폐동맥 판막 치환술을 시행하였으며, 병리조직학적 검사에서 폐동맥 육종으로 진단되었다.

A Case of Pleural Hydatid Cyst Mimicking Malignancy in a Non-Endemic Country

  • Kim, Se-Joong;Jung, Ki-Hwan;Jo, Won-Min;Kim, Young-Sik;Shin, Chol;Kim, Je-Hyeong
    • Tuberculosis and Respiratory Diseases
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    • 제70권4호
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    • pp.338-341
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    • 2011
  • Hydatid disease is caused by the larval stage of taenia $Echinococcus$, which endemic in the Mediterranean region. Recently, the prevalence of the disease has increased worldwide due to an increase in the frequency of travel and immigration. As the infested larvae migrate through the bloodstream, the final destination is most commonly the liver or lungs; direct pleural invasion is very rare. A 50-year-old diabetic Korean man presented with an incidentally noted 2 cm right pleural nodule. On follow up imaging after three months, its size had increased. To confirm the diagnosis of the lesion, surgical excision was performed. Histopathological examination showed the diagnosis of a hydatid cyst. The patient had no history of overseas travel, but lives in an urban area where many foreign workers from endemic countries reside. This is the first reported case of primary pleural hydatid disease in a non-endemic country.

심장종양 6례 보고 (Cardiac Tumors)

  • 김병주
    • 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.

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나비굴경유 수술을 통해 완치된 뇌하수체 거대선종에 동반된 쿠싱병 1예 (Treatment of Cushing's disease with macroadenoma through transsphenoidal surgery)

  • 이상아;문재철
    • Journal of Medicine and Life Science
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    • 제18권1호
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    • pp.16-19
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    • 2021
  • Cushing's disease (CD) is a rare illness characterized by chronic hypercortisolism secondary to the overproduction of adrenocorticotropic hormone by a pituitary adenoma, which is associated with a high risk of developing serious complications, such as diabetes mellitus, cardiovascular disease, and emotional disorders. Endoscopic transsphenoidal surgery is performed for the treatment of CD, and was initially preferred over other types of treatments. However, the recurrence after pituitary surgery for CD is a common problem after an initial successful surgery. In microadenomas, the remission rates were higher than those of macroadenoma. This patient had a giant tumor that was greater than 4 cm in length on sella magnetic resonance imaging, and panhypopituitarism was detected using a combined pituitary stimulation test. After transsphenoidal surgery, the patient required temporary hormone replacement for a short period of time. After 1 year, he showed a normal cortisol response on the overnight dexamethasone suppression test and low morning cortisol levels. Therefore, we indicated that the patient was cured of giant macroadenoma with panhypopituitarism before surgery, and thus, reported this case.

Infective Costochondritis after Augmentation Mammoplasty: A Rare Case Report and Review of the Literature

  • Sally Min;Jinil Choi;Kwon Joong Na;Ki Yong Hong
    • Archives of Plastic Surgery
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    • 제50권5호
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    • pp.488-491
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    • 2023
  • Silicone breast implant insertion is a commonly performed surgical procedure for breast augmentation or reconstruction. Among various postoperative complications, infection is one of the main causes of patient readmission and may ultimately require explantation. We report a case of infective costochondritis after augmentation mammoplasty, which has rarely been reported and is therefore difficult to diagnose. A 36-year-old female visited the clinic for persistent redness, pain, and purulent discharge around the left anteromedial chest, even after breast implant explantation. Magnetic resonance imaging showed abscess formation encircling the left fourth rib and intracartilaginous and bone marrow signal alteration at the left body of the sternum and left fourth rib. En bloc resection of partial rib and adjacent sternum were done and biopsy results confirmed infective costochondritis. Ten months postoperatively, the patient underwent chest wall reconstruction with an artificial bone graft and acellular dermal matrix. As shown in this case, early and aggressive surgical debridement of the infected costal cartilage and sternum should be performed for infective costochondritis. Furthermore, delayed chest wall reconstruction could significantly contribute to the quality of life.