• 제목/요약/키워드: Segmental resection

검색결과 125건 처리시간 0.034초

골육종에 시행한 Kotz prosthesis의 역학적 실패 - 증례 보고 - (Mechanical Failure of Kotz Prosthetic Replacement for Osteosarcoma - A Case Report -)

  • 조덕연;김희천;심면보
    • 대한골관절종양학회지
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    • 제2권1호
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    • pp.101-105
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    • 1996
  • Prosthetic reconstruction of musculoskeletal defects about the knee for tumor has many advantages, particularly the maintenance of motion and immediate functional restoration. But, prosthetic reconstruction has inherent limitations in terms of long-term durability. The authors have reported here a patient who had mechanical failure at 61 months later following use of a modular resection system to reconstruct the segmental defect of proximal tibia in osteosarcoma. In this case, another technique of extensor mechanism reconstruction using Achilles tendon allograft was attempted. Because of the concerns involving durability of tumor prosthesis, increased emphasis has to be placed on innovation in prosthetic design.

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선천성 영아 섬유육종 (Congenital Infantile Fibrosarcoma)

  • 김태형;정재희;송영택
    • Advances in pediatric surgery
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    • 제10권1호
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    • pp.52-55
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    • 2004
  • A newborn male baby was transferred to our hospital with a left inguinal mass. The mass was huge measuring $10{\times}10cm$, engorged, and dark-blue colored as a result of internal hemorrhage. Unstable vital signs were combined with DIC and acute renal failure. Emergency operation was performed because of the suspicion of bowel perforation. The peritoneal cavity was full of ascitis and the distal jejunum had a 0.5 cm perforation. Segmental resection of the jejunum and incisional biopsy of the inguinal mass were performed. On pelvic and thigh MRI, the mass protruded into pelvic cavity and encircled large vessels and nerves of the thigh. Pathologic diagnosis was congenital infantile fibrosarcoma. Fifteen days after operation, primary tumor excision was undertaken. The second look operation, performed after 6 times VAC chemotherapy, revealed no remained malignant cell on microscopic section. The baby has been followed closely for the last eight months.

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Glomangiomyoma of the Trachea

  • Baek, Sam-Hyun;Huh, Dong-Myung;Park, Jun-Ho;Kwak, Eun-Kyoung;Kim, Byung-Ho;Han, Won-Kyung
    • Journal of Chest Surgery
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    • 제44권6호
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    • pp.440-443
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    • 2011
  • A glomus tumor is an uncommon soft tissue tumor that is most commonly found in the subungual area and a glomus originating in the trachea is extremely rare. Histologically and ultrastructurally, these tumors have been divided into three subtypes: classic glomus tumors, glomangiomas, and glomangiomyomas. Glomangiomyomas account for less than 10% of all glomus tumors and are the least common type. We report a case of a 54-year-old man with glomangiomyoma of the trachea who presented with stridor. We treated the tumor by segmental resection and primary repair via a transcervical approach.

Small Bowel Injury as a Complication of Lumbar Microdiscectomy : Case Report and Literature Review

  • Kim, Duk-Sung;Lee, Jung-Kil;Moon, Kyung-Sub;Ju, Jae-Kyun;Kim, Soo-Han
    • Journal of Korean Neurosurgical Society
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    • 제47권3호
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    • pp.224-227
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    • 2010
  • Small bowel injury resulting from unforeseen penetration of the anterior annulus fibrosus and longitudinal ligament is a rare complication of lumbar microdiscectomy. The patient complained of abdominal tenderness and distention immediately after microdiscectomy for L4-5 and L5-S1 disc herniation. Using abdominal computed tomography, we found several foci of air overlying the anterior aspect of the vertebral body at the L5-S1 level. Segmental resection of the small bowel including small tears and primary anastomosis of the jejunum were performed. Here, we present a case of intestinal perforation after lumbar microdiscectomy and discuss technical methods to prevent this complication with a review of literature.

A Case of Primary Endobronchial Neurilemmoma Without Intraspinal Extension

  • Kim, Mi-Young;Kim, Hyun-Ji;Kim, Ah-Lim;Kim, Hyeong-Seok;Shin, Hyun-Woong;Jeong, Seung-Wook
    • Journal of Yeungnam Medical Science
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    • 제29권1호
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    • pp.54-57
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    • 2012
  • Neurilemmoma is a benign and slowly growing neurogenic tumor. Intrathoracic neurilemmoma often develops in the chest wall and posterior mediastinum, but endobronchial neurilemmoma is extremely rare. The diagnosis of endobronchial neurilemmoma with preoperative imaging findings is challenging and is usually made via postoperative pathological examination. These authors encountered a case of primary endobronchial neurilemmoma in a 52-year-old woman who had no symptoms. A $3.0{\times}2.6$ cm mass in the right lower lobe projecting into the mediobasal segmental bronchus was shown in the results of the contrast-enhanced computed tomography (CT) and magnetic resonance imaging (MRI) of the chest. Benign neurilemmoma was confirmed via bronchoscopic biopsy, and surgical resection (sleeve bronchial excision and end-to-end anastomosis) was performed.

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폐에 발생한 점막 표피양 종양 - 1예 보고 - (Mucoepidermoid Carcinoma of the lung -A case report -)

  • 윤경찬;박이태
    • Journal of Chest Surgery
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    • 제37권1호
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    • pp.92-94
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    • 2004
  • 폐에 발생하는 점막 표피양 종양은 매우 드물며, 대부분 주로 주기관지에서 발생한다. 증상은 주로 기관 자극이나 폐쇄에 의해 발생된다. 점막 표피양 종양이 원격전이 되는 경우는 흔하지 않다. 치료는 수술적 제거가 원칙이며 예후는 종양의 조직학적 소견과 밀접한 관계가 있다. 저자의 경우 우중엽에 발생한 점막 표피양 종양을 우중엽절제술로 치험하여 양호한 결과를 보였기에 이에 보고하는 바이다.

폐과오종의 외과적 치료 (Surgical Treatment of Pulmonary Hamartoma)

  • 김웅한;성숙환;김주현
    • Journal of Chest Surgery
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    • 제27권3호
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    • pp.215-220
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    • 1994
  • From Jan. 1981 to Dec. 1993, 24 cases of pulmonary hamartoma were experienced sugically at the Department of Thoracic Surgery, College of Medicine, Seoul National University. They consisted of 11 females and 13 males. The age distribution was 24 years to 71 years with a mean age of 49 years. They included 3 cases of endobronchial hamartoma, and 21 cases of pulmonary parenchymal hamartoma. Fifty eight percent of patients [14/24] were asymptomatic. One patient had a multiple pulmonary parenchymal hamartoma, and 1 patient also had combined lung cancer. The operative procedures were 9[37.5%] wedge resections, 5[20.8%] lobectomies, 3[12.5%] enucleations, 3[12.5%] segmental resections, 2[8.3%] bilobectomies, 1[4.2%] lobectomy and segmentectomy, and 1[4.2%] lobectomy, wedge resection, and enucleation. All of the operative results were excellent and without complication.

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우상엽의 허탈을 동반한 기관지 폐쇄증 -1례 보고 (Bronchial Atresia with Collapse of the Right Upper Lobe -A Case Report)

  • 김성호;장인석
    • Journal of Chest Surgery
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    • 제30권8호
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    • pp.843-846
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    • 1997
  • 서처성 기관지 폐쇄증은 발생학적으로 태아의 어떤 시기에 기관지 계통에 대한 혈관이 차단됨으로 인해 유발된다고 여겨지는 아주 드문 폐-기관지 질환의 하나로, 이 질환은 주기관지와 쒜구역 또는 페엽 사이에 기도의 연결이 되어 있지 않은 이상증으로 정의된다. 그간 보고된 모든 경우의 기관지 폐쇄증은 측부 순환 이 In재함으로 인해 폐쇄된 폐구역이나 페엽이 흉부 단순 촬영상 과투과 음영을 보였다고 하였으나, 본원에 서는 그간 이론적으로만 가능하다고 했던 폐염의 허탈을 동반한 기관지 폐쇄증을 수술 치험하였기에 보고하 는 바이다.

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구강 및 구인두암의 수술에 있어서 하악골 부분절제술에 대한 고찰 (Partial Mandibulectomy for Oral Cavity and Oropharyngeal Carcinoma)

  • 최은창;홍원표
    • 대한두경부종양학회지
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    • 제10권2호
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    • pp.163-170
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    • 1994
  • Segmental mandibulectomy causes severe functional disability and cosmetic problem. Many methods of reconstruction have been used but none of these procedures provides the ideal solution. There has been increased interest in the possibility of preserving a portion of the mandible and still carrying out a adequate tumor resection. We experienced four cases of marginal with sagittal mandibulectomy in patients with floor of mouth. buccal. and soft palate carcinoma, and sagittal mandibulectomy in 8 patients with tonsillar carcinoma and a case of marginal mandibulectomy in tonsillar cancer patient. In all cases mandible facing the tumor were successfully resected and repair of the mandible. postoperative facial contour were satisfactory. We think. that these sagittal procedures are oncologically sound in its removal of tumor. biomechanically secure and maximize postoperative rehabilitation while maintaining the normal contour of the face.

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수포성 표피박리증을 동반한 선천성 유문부폐쇄증 1예 (Congenital Pyloric Atresia with Junctional Epidermolysis Bullosa-a case report)

  • 조마해;한석주
    • Advances in pediatric surgery
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    • 제3권1호
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    • pp.77-82
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    • 1997
  • The association of pyloric atresia and epidermolysis bullosa(EB) in newborn is rare and inheritant as an autosomal recessive trait. We report a newborn girl with pyloric atresia and epidermolysis bullosa. Blisters were noted on her skin at birth, especially in pressure-exposed area, and later on the oral mucosa. Junctional epidermolysis bullosa was confirmed by light microscopy and electron microscopy. Radiography revealed pyloric atresia. Segmental resection of 1.5 cm and gastroduodenostomy were carried out at 4 days of age. Protein loosing enteropathy developed after oral feeding. The frequency of episodes of nonscarred blisters and the severity and duration improved significantly with time. The protein loosing enteropathy was persistent, and at 1 year of age, her growth is markedly retarded.

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