• 제목/요약/키워드: subtotal resection

검색결과 108건 처리시간 0.031초

The Impact of Esophageal Reflux-Induced Symptoms on Quality of Life after Gastrectomy in Patients with Gastric Cancer

  • Im, Min Hye;Kim, Jong Won;Kim, Whan Sik;Kim, Jie-Hyun;Youn, Young Hoon;Park, Hyojin;Choi, Seung Ho
    • Journal of Gastric Cancer
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    • 제14권1호
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    • pp.15-22
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    • 2014
  • Purpose: To evaluate the prevalence of esophageal reflux-induced symptoms after gastrectomy owing to gastric cancer and assess the relationship between esophageal reflux-induced symptoms and quality of life. Materials and Methods: From January 2012 to May 2012, 332 patients were enrolled in this cross-sectional study. The patients had a history of curative resection for gastric cancer at least 6 months previously without recurrence, other malignancy, or ongoing chemotherapy. Esophageal reflux-induced symptoms were evaluated with the GerdQ questionnaire. The quality of life was evaluated with the European Organization for Research and Treatment QLQ-C30 and STO22 questionnaires. Results: Of the 332 patients, 275 had undergone subtotal gastrectomy and 57 had undergone total gastrectomy. The number of GerdQ(+) patients was 58 (21.1%) after subtotal gastrectomy, and 7 (12.3%) after total gastrectomy (P=0.127). GerdQ(+) patients showed significantly worse scores compared to those for GerdQ(-) patients in nearly all functional and symptom QLQ-C30 scales, with the difference in the mean score of global health status/quality of life and diarrhea symptoms being higher than in the minimal important difference. Additionally, in the QLQ STO22, GerdQ(+) patients had significantly worse scores in every symptom scale. The GerdQ score was negatively correlated with the global quality of life score (r=-0.170, P=0.002). Conclusions: Esophageal reflux-induced symptoms may develop at a similar rate or more frequently after subtotal gastrectomy compared to that after total gastrectomy, and decrease quality of life in gastric cancer patients. To improve quality of life after gastrectomy, new strategies are required to prevent or reduce esophageal reflux.

췌장 두부 또는 십이지장을 침범한 위암에서의 수술적 치료 (Surgical Treatment of Gastric Cancer Invading the Pancreatic Head or Duodenum)

  • 김수열;이종명;김우영
    • Journal of Gastric Cancer
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    • 제7권4호
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    • pp.193-199
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    • 2007
  • 목적: 주위 장기를 침범한 진행성 위암에서 병소의 완전한 절제를 위해서는 침범된 장기의 합병 절제가 필수적이다. 그러나 종양이 췌장 두부나 십이지장물 침범하는 경우에는 낮은 절제 성공과 높은 이환율로 인하여 병소의 완전한 절제는 제한된다. 이에 저자들은 췌장 두부 또는 십이지장을 침범한 위암에서 시행된 수술 방법을 후향적으로 분석하여 수술 방법 선정의 적절성을 알아보고가 하였다. 대상 및 방법: 1998년 1월부터 2003년 12월까지 5년가 예수병원 외과에서 위선암으로 진단되어 수술을 시행한 환자 중 수술 소견상 원발 종양이나 구역 림프절에 의해 췌장 두부나 십이지장의 침범이 의심되는 45명의 환자 중 비치유 인자를 동반하지 않은 22예를 대상으로 후향적 연구를 시행하였다. 합병 절제를 시행한 4예를 PD군, 위아전절제술만을 시행한 12예를 STG군, 고식적 우회술만을 시행한 6예를 GJ군으로 분류하였다. 각 군에서 임상병리학적 특성 및 수술적 자료를 비교 분석하였다. 결과: PD군은 모두 D3 림프절 절제술을 포함하는 췌십이지장절제술을 시행하여 병소의 완전한 절제를 하였으며, 1예에서 췌장루를 보였고(이환율 25%) 수술로 인할 사망 예는 없었다(사망률 0%), PD군은 모두 제 IV 병기였으나 75%의 2년 생존율과 50%의 5년 생존율을 보였다. STG군은 종양을 변연 절제(marginal resection)하거나 (6예) 고식적 절제술을 시행하였으며(6예) 림프절 절제의 범위도 D2 이하로 적었고 41.7%의 2년 생존율과 16,7%의 5년 생존율 보였다. GJ군은 평균 연령이 $72.7{\pm}8.6$세로 고랑이었으며 2년 생존율이 0%였다. 결론: 췌장 두부를 침범한 진행성 위선암에서 합병 절제로서의 췌십이지장절제는 중등도 이환율과 낮은 사망률로 비교적 안전하게 시행될 수 있고 비치유 인자가 없는 경우 장기 생존을 기대할 수 있는 술식으로 생각된다.

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두경부종양 치료 후 발생한 결손의 피판 및 복합조직이식을 이용한 재건 (Immediate Reconstruction of Defects Developed After Treatment of Head and Neck Tumors Using Cutaneous and Composite Flaps)

  • 탁관철;이영호;류재덕
    • 대한두경부종양학회지
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    • 제1권1호
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    • pp.35-61
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    • 1985
  • The surgical treatment of advanced carcinomas and some benign tumors having clinically malignant behaviors of the head and neck region often require extensive resection, necessitating large flaps for reconstruction. Since the original upper arm flap was described by Tagliacozzi in 1597, a variety of technique such as random pattern local flap, axial flap, distant flap, scalping flap, myocutaneous flap, free flap etc. have been proposed for reconstruction of head, face and neck defects. Reconstruction of the facial defects usually require the use of distant tissue. Traditionally, nasal reconstruction has been carried out with a variety of forehead flaps. In recent years, there has been more acceptance of immediate repairs following the removal of these tumors. As a result, patients are more willing to undergo these extensive resections to improve their chances of cure, with the reasonable expectation that an immediate reconstruction will provide an adequate cosmetic result. Authors experienced 13 cases of head and neck tumor during last three and half years that required wide excision and immediate reconstruction with various flaps, not with primary closure or simple skin graft. We present our experience with varied flaps for reconstruction after wide resection of head and neck tumors 3 cases of defect of dorsum of nose or medial canthus with island forehead flaps, lower eyelid defect with cheek flap, cheek defect with Limberg flap, orbital floor defect with Temporalis muscle flap, lateral neck defects with Pectoralis major myocutaneous flap or Latissimus dorsi myocutaneous free flap, subtotal nose defect with scalping flap, wide forehead defect with Dorsalis pedis free flap and 3 cases of mandibular defect or mandibular defect combined with lower lip defect were reconstructed with free vascularized iliac bone graft or free vascularized iliac bone graft concomitantly combined with free groin flap pedicled on deep circumflex iliac vessels We obtained satisfactory results coincided wi th goal of treatment of head and neck tumors, MAXIMAL CURE RATE with MINIMAL MORBIDITY, OPTIMAL FUNCTION, and an APPEARANCE as close to normal as possible.

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Primary Malignant Melanoma in the Pineal Region

  • Park, Jae-Hyun;Hong, Yong-Kil
    • Journal of Korean Neurosurgical Society
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    • 제56권6호
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    • pp.504-508
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    • 2014
  • A 59-year-old male patient had 5-month history of gait disturbance and memory impairment. His initial brain computed tomography scan showed $3.5{\times}2.8cm$ sized mass with high density in the pineal region. The tumor was hypointense on T2 weighted magnetic resonance images and hyperintense on T1 weighted magnetic resonance images with heterogenous enhancement of central portion. The tumor was totally removed via the occipital transtentorial approach. Black mass was observed in the operation field, and after surgery, histopathological examination confirmed the diagnosis of malignant melanoma. Whole spine magnetic resonance images and whole body 18-fluoro-deoxyglucose positron emission tomography could not demonstrate the primary site of this melanoma. Scrupulous physical examination of his skin and mucosa was done and dark pigmented lesion on his left leg was found, but additional studies including magnetic resonance images and skin biopsy showed negative finding. As a result, final diagnosis of primary pineal malignant melanoma was made. He underwent treatment with the whole brain radiotherapy and extended local boost irradiation without chemotherapy. His preoperative symptoms were disappeared, and no other specific neurological deficits were founded. His follow-up image studies showed no recurrence or distant metastasis until 26 weeks after surgery. Primary pineal malignant melanomas are extremely rare intracranial tumors, and only 17 cases have been reported since 1899. The most recent case report showed favorable outcome by subtotal tumor resection followed by whole brain and extended local irradiation without chemotherapy. Our case is another result to prove that total tumor resection with radiotherapy can be the current optimal treatment for primary malignant melanoma in the pineal region.

외과적 절제술로 치험한 갑상선암 194예의 임상적 고찰 (A Clinical Study of Surgically Treated 194 Cases of the Thyroid Cancer)

  • 이석재;김성배;김상호
    • 대한두경부종양학회지
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    • 제18권1호
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    • pp.50-55
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    • 2002
  • Objectives: Thyroid cancer is the most common endocrine malignancy with favorable histologic and prognostic characteristics. Total or near total thyroidectomy has been used as a standard surgical procedure. The aims of this study are to determine the extent of resection of thyroid gland and to find the influencing factors of lymph node metastasis. Materials and Methods: The authors reviewed the records of 194 patients of thyroid cancer surgically treated at Department of General Surgery, Inje University Busan Paik Hospital from January, 1996 to December, 2000. Pathologic classifications, surgical procedures, and lymph node metastasis were analyzed. Results: There were 163 women and 31 men. The age ranged from 12 to 79 years old (mean age 43.2 years). The histological classifications of 194 cases revealed papillary cancer in 171 cases (88.1%), follicular cancer in 17 cases (8.8%), undifferentiated cancer in 3 cases (1.6%), medullary cancer in 2 cases (1.0%) and mixed cancer in 1 case (0.5%). Among the 194 patients, lobectomy was perfomed in 31 patients, subtotal thyroidectomy in 30 patients, near total thyroidectomy in 82 patients and total thyroidectomy in 51 patients. In the subgroup of papillary carcinoma 141 cases with lymph node dissection, lymph node metastasis had no statistical significance according to sex, age and primary tumor size. Conclusions: The mainly performed surgical procedures were total thyroidectomy and near total thyroidectomy. In thyroid cancer surgery, the extent of resection was influenced by age, differentiation and primary tumor size. The lymph node dissection should be decided by lymph node metastasis identified by preoperative radiologic evaluation or intraoperative lymph node findings.

IgG4-related Disease in the Stomach which Was Confused with Gastrointestinal Stromal Tumor (GIST): Two Case Reports and Review of the Literature

  • Seo, Ho Seok;Jung, Yoon Ju;Park, Cho Hyun;Song, Kyo Young;Jung, Eun Sun
    • Journal of Gastric Cancer
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    • 제18권1호
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    • pp.99-107
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    • 2018
  • Immunoglobulin G4-related disease (IgG4-RD) is an immune-mediated fibro-inflammatory disorder characterized by specific pathological findings and elevated serum IgG4 level. IgG4-RD in the stomach is rare, and occasionally diagnosed as gastric subepithelial tumor (SET) by endoscopy or computed tomography scan. Two female patients in the age group of 40-50 years were diagnosed with 4 cm sized gastric SET. One underwent laparoscopic gastric wedge resection. Another one had a history of subtotal gastrectomy for early gastric cancer and idiopathic thrombocytopenic purpura with oral steroids administration. She underwent a completion total gastrectomy with splenectomy for the gastric SET and ITP. The pathology showed storiform fibrosis, and IgG4 was positive in immunohistochemistry (IHC) stain. IgG4-RD is known as a medical disease that could be treated with oral steroids. The difficulty in preoperative diagnosis of the disease occasionally causes unnecessary gastric resection. Thus, preoperative diagnostic methods for IgG4-RD such as deep biopsy with IHC stain or magnetic resonance imaging are needed.

소아 시교차-시상하부 신경교종의 치료 (Management of Chiasmatic-Hypothalamic Gliomas in Children)

  • 도홍직;김일만;이창영;손은익;김동원;임만빈;김상표
    • Journal of Korean Neurosurgical Society
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    • 제30권9호
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    • pp.1115-1119
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    • 2001
  • Objective : Management strategies for pediatric chiasmatic-hypothalamic gliomas(CHG) include surgery, irradiation, chemotherapy and a combination of these modalities. This study was performed in order to compare the efficacy of various methods of treatment and to describe its optimal management. Material and Method : We have reviewed the results of management of 6 children with a diagnosis of CHG, who were observed closely during the last 8 years. The patients were aged 7 months to 15 years. Our patients presented with diencephalic syndrome, endocrine dysfunction, and progressive visual loss. None of these had evidence of neurofibromatosis-1. Treatment consisted of surgery alone(2), surgry and irradiation(2), surgery, irradiation and chemotherapy(1), and surgery and chemotherapy(1). Results : Four children had large exophytic suprasellar tumors and two showed diffuse midline lesions. Obstructive hydrocephalus was present in all patients. Pathologic examination revealed anaplastic astrocytoma in 1 and lowgrade astrocytoma in 5. Two patients, recently treated with radiation therapy following radical subtotal resection, showed significant tumor reductions and good clinical status. Four patients had partial tumor resection. Of these patients, two developed disease stabilization during follow-up period of 7 and 8 years, respectively. Life-threatening complications were noted in remaining two patients. Conclusion : CHG may follow an unpredicatable course and show a various reponse to each treatment modality. Further studies are indicated to define the optimal method of treatment of CHG in childhood.

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소아 췌장종양의 임상적 고찰 (Clinical Experiences of Pancreatic Tumors in Children)

  • 임라주;김해솔;김태석;이철구;서정민;이석구
    • Advances in pediatric surgery
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    • 제13권2호
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    • pp.155-161
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    • 2007
  • Pancreatic tumors in children are very rare but have a better prognosis compared with that in adult. Pediatric pancreatic tumors are more often benign and easier to resect. To evaluate the characteristics and prognosis, the records of 13 patients who underwent pancreatic resection, from June 1997 to May 2005, at Samsung Medical Center were reviewed. The mean follow up period was 48 months. The male to female ratio was 1: 1.6. Mean age was 10.3 years. Signs and symptoms included abdominal pain (7), abdominal palpable mass (5), jaundice (1), hypoglycemic (1), and non-specific GI symptoms (4). The commonly used diagnostic tools were CT and abdominal sonography. In addition, MRI, ERCP, EEG, and hormone test were also done when indicated. Surgical procedures included distal pancreatectomy (5), pylorus preserving pancreaticoduodenectomy (4), tumor excision (3), and subtotal pancreatectomy (1). Locations of lesions in pancreas were head (4), tail (5), and body and tail (4). Postoperative complications developed in 3 cases; postoperative ileus (1), wound problem (1), and pancreatitis (1). The pathologic diagnosis included solid-pseudopapillary tumor (6), congenital simple cyst (1), pancreatic duplication cyst (1), serous oligocystic adenoma (1), mucinous cystadenocarcinoma (1), rhabdomyosarcoma (1), insulinoma (1), and pancreatoblastoma (1). Three cases received adjuvant chemotherapy and radiotherapy. Overall survival rate was 81 %. One patient with a mucinous cystadenocarcinoma died. In this study, pancreatic tumors in children were resectable in all patients and had good survival. Surgery of pancreatic tumors should be regarded as the gold standard of treatment and a good prognosis can be anticipated in most cases of benign and malignant tumors.

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Prognostic Factors Affecting Surgical Outcomes in Squamous Cell Carcinoma of External Auditory Canal

  • Nam, Gi-Sung;Moon, In Seok;Kim, Ji Hyung;Kim, Sung Huhn;Choi, Jae Young;Son, Eun Jin
    • Clinical and Experimental Otorhinolaryngology
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    • 제11권4호
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    • pp.259-266
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    • 2018
  • Objectives. Carcinomas of the external auditory canal (EAC) are rare, and management remains challenging. Previous studies seeking prognostic factors for EAC cancers included cancers other than carcinomas. In this study, we analyzed the treatment outcomes of, prognostic factors for, and survival rates associated with specifically squamous cell carcinoma (SCC) of the EAC. Methods. A retrospective review of 26 consecutive patients diagnosed with SCCs of the EAC in a 10-year period was performed in terms of clinical presentation, stage, choice of surgical procedure, and adjunct therapy. Overall survival (OS) and recurrence-free survival (RFS) were calculated and univariate analysis of prognostic factors was performed. Results. The median age of the 26 patients with SCCs of the EAC was 63 years (range, 40 to 72 years), and 16 males and 10 females were included. According to the modified University of Pittsburgh staging system, the T stages were T1 in 11, T2 in six, T3 in four, and T4 in five cases. The surgical procedures employed were wide excision in three cases, lateral temporal bone resection (LTBR) in 17, and extended LTBR in four, and subtotal temporal bone resection in two. Two patients underwent neoadjuvant chemotherapy, and two underwent adjuvant chemotherapy. One patient received preoperative radiation therapy, and eleven received postoperative radiation therapy. Of the possibly prognostic factors examined, advanced preoperative T stage and advanced overall stage were significant predictors of RFS, but not of OS. Conclusion. The advanced T stage and overall stage were associated with decreased survival after surgical treatment in patients with SCC of the EAC, highlighting the importance of clinical vigilance and early detection.

흉선종의 방사선치료 : 예후인자 및 치료성적 (Prognostic Factors and Treatment Outcome for Thymoma)

  • 김학재;박찬일;신성수;김주현;서정욱
    • Radiation Oncology Journal
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    • 제19권4호
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    • pp.306-311
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    • 2001
  • 목적 : 흉선종에 있어서 수술과 방사선치료에 따른 결과와 생존율에 영향을 주는 여러 예후인자를 파악하기 위하여 후향적 연구를 시행하였다. 방법 : 1979년부터 1998년까지 서울대학병원에서 수술과 방사선치료를 받은 55명의 환자를 대상으로 하였다. 그 중 수술만 받은 환자는 11명, 수술 후 방사선치료를 받은 환자는 33명이었고, 방사선치료만을 받은 환자는 11명이었다. 추적 관찰 기간은 $2\~160$개월(중앙값:64개월)이었다. 남녀의 구성비는 1:1, 대상 환자의 연령은 $15\~74$세(중앙값:48세)였다. 종양의 크기와 조직학적 분류, 병기, 수술의 범위 정도, ECOG활동도, 종양 수반 증후군, 치료 방법에 따라 생존율을 분석하였다. 통계방법은 생존율은 Kaplan-Meier, 생존율의 차이는 log rank test, 다변수 분석은 Cox regression 방법을 이용하였다. 결과 : 전체 환자의 5년 생존율은 $87\%$, 10년 생존율은 $65\%$이었고, 중앙생존기간은 103개월이었다. 단변량분석상 생존에 통계적으로 유의한 예후인자는 병기(p=0.0017)였고, 다변량분석상에서도 역시 병기(p=0.0007) 만이 유일한 예후인자였다. 결론 : 흉선종에 있어서 병기가 주요 예후인자임을 알 수 있었고, 특히 수술의 절제 범위가 생존율과 무병생존율에 큰 영향을 주므로 완전절제를 하는 것이 생존율을 높일 수 있을 것으로 생각된다.

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