• 제목/요약/키워드: Without systemic involvement

검색결과 33건 처리시간 0.035초

국소 재발된 유방암의 방사선치료 (Radiotherapy in Locoregional Recurrent Breast Carcinoma)

  • 하성환;양미경;정웅기;박찬일;방영주;김노경;최국진
    • Radiation Oncology Journal
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    • 제6권2호
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    • pp.203-209
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    • 1988
  • 국소적으로 재발된 유방암의 경우, 근래에 와서 치료법의 발다로 관해율도 증가되고, 또한 환자의 수명도 연장시킬 수 있다는 보고가 증가되고 아울러 관심도 높아지고 있는 상태이다. 따라서 이런 국소 재발된 유방암을 가진 환자의 특성과 치료에 대한 실패양상, 그리고 예후에 영향을 미치는 인자들을 분석하여 이들 환자에 대한 치료에 도움이 되고자, 서울대학교 병원에서는 1979년에서 1986년까지 치료받은 총 33예에 대해서 분석을 하여 다음과 같은 결과를 얻었다. 15예(45%)에서 흉벽에 국한되어 재발하였고, 18예가 임파절에 재발을 하였다. 초기 치료후 36개월만에 87%가 재발을 보였다. 원전절제를 받아 방사선치료에 대한 판정을 할 수 없었던 8예를 제외한 25예에서 72%(18예)가 방사선치료 후 완전관해를 보였다. 국소재발 후 3년 동안의 생존율은 50%였다. 초기 치료후 2년이내 재발한 환자들의 3년 생존율은 24%였고, 2년 이후 재발한 경우는 100%였다. 흉벽에만 재발한 경우, 3년 생존율은 57%였고, 임파절에만 재발한 경우는 43%였다. 후자의 경우 대부분이 원격전이를 보였다. 완전관해를 보인 예와, 그렇지 않은 예에서는 각각 63%의 3년 생존율, 그리고 33%의 1년 생존율을 보였다. 3명의 환자가 대측 유방에 암을 보였다. 원발성 유방암에 대해서 수술과 전신치료를 함께 받은 경우 3년 생존율이 40%였고, 수술만 시행한 경우는 71%였다. 방사선 치료후 후속적 재발을 보인 경우의 2년 생존율은 25%였다.

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난치성 애역 환자를 팔정산으로 치료한 1례 (A Case of Intractable Hiccup Treated with Paljung-san)

  • 신원용;최은영;현진오;윤철호;임성우;한창호;이원철;현민경
    • 대한한방내과학회지
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    • 제26권2호
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    • pp.506-511
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    • 2005
  • Hiccup is a common clinical symptom, and may be caused from over 100 medical origins. Generally hiccup happens temporarily, and continues only a few seconds or minutes, and is cured easily by physical methods or even by itself. But in some cases, hiccup is so refractory that patients may be tired and very troubled by it. At worst, it may cause death. Intractable hiccup is defined as hiccup persisting for more than 48 hours, and this appears in various diseases. Persistent hiccup is very difficult to treat by conventional methods. A 69-year-old man was admitted due to intractable hiccup without gastroenteral system abnormalities or peripheral nervous systemic involvement. So Paljung-san(八正散) was prescribed. The intensity and frequency of hiccup dramatically improved.

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완전관해 후 중추신경계에 재발한 골수외 형질세포종 (Relapsed plasmacytoma in central nervous system after complete remission of extramedullary plasmacytoma)

  • 강선미;김성규;서지호;김지윤;성우정;배성화;류헌모
    • Journal of Yeungnam Medical Science
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    • 제31권1호
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    • pp.43-47
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    • 2014
  • Extramedullary plasmacytoma (EMP) is a rare disease that occurs in 3% to 5% of patients with plasma cell disorder. It occurs most commonly in the upper respiratory tract and the oral cavity. Very few EMP cases have been reported in the central nervous system (CNS). We report herein an unusual case of EMP in the nasal cavity that recurred in the CNS without systemic involvement. A 67-year-old man visited our hospital due to a month-long bout with exophthalmos. He was diagnosed with EMP in the nasal cavity, paranasal sinus, and orbital cavity. He received radiotherapy to which he had complete responses. After 2 years, he visited our hospital because of a month-long headache. He was diagnosed with EMP recurrence in the CNS via brain magnetic resonance imaging and cerebrospinal fluid analysis. He was treated with whole brain radiotherapy and intrathecal chemotherapy with methotrexate, but he expired due to pneumonia.

Henoch-Sch$\ddot{o}$nlein 자반병 신염으로 의심했던 현미경적 다발혈관염 1례 (A Case of Microscopic Polyangiitis Initially Suspected with Henoch-Sch$\ddot{o}$nlein Purpura Nephritis)

  • 임종근;문경철;구자욱
    • Childhood Kidney Diseases
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    • 제16권2호
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    • pp.132-137
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    • 2012
  • Henoch-Sch$\ddot{o}$nlein 자반병 신염과 유사한 증상을 가지는 10세 여자에게 발생한 급격한 신기능 저하를 동반하지 않은 현미경적 다발혈관염 1례를 경험하였기에 보고하는 바이다. 이 혈관염의 경우. 진단 시점 또는 치료 시작할 때의 신장기능 저하가 심할수록 병의 예후가 나쁘므로[20], 사구체 여과율이 떨어지기 전에 빠른 진단과 치료가 필요하다. Henoch-Sch$\ddot{o}$nlein 자반병이 의심될 경우 단백뇨와 혈뇨가 지속되면, 다른 혈관염과의 감별을 위해 ANCA, 신장 조직검사가 도움을 줄 것으로 생각된다.

자궁 경부암의 수술후 방사선 치료에서 선량 분포에 관한 연구 (A Study of Dose Distribution in Postoperative Radiotherapy in Uterine Cervical Cancer)

  • 신세원;김성규;김명세
    • Journal of Yeungnam Medical Science
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    • 제8권1호
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    • pp.166-177
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    • 1991
  • 1986년 4월부터 1991년 3월까지 영남대학교 의과대학 부속병원에서 자궁 경부암으로 확진되어 수술후 방사선치료를 시행한 22명의 환자에서 방사선 선량 분포에 따른 치료성적은 다음과 같다. 1. 22명중 3명(13.6%)에서 골반이나 복부에 재발이 생겼으며 임상적 병기가 진행될수록, 외부조사선량이 적을수록 재발이 많았다. 2. 골반내 임파선 전이와 임파혈관 침범인 경우에 재발이 되었다. 3. 강내조사 선량이나 수술방법은 재발과 무관하였다. 4. 중대한 합병중은 임상적 병기가 앞설수록 외부조사 선량이나, 총조사 선량이 증가할수록 많이 발생하였다. 이상의 결과를 보면 본원 치료방사선과의 자궁 경부암의 수술후 방사선 치료원칙은 적절하며 재발방지와 합병증의 예방을 위한 세심한 주의와 항암제를 위시한 전신요법의 추가를 고려하여야 하겠다.

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Primary Squamous Cell Carcinoma of the Remnant Stomach after Subtotal Gastrectomy

  • Chang, Yeon Soo;Kim, Min Sung;Kim, Dong Hee;Park, Seulkee;You, Ji Young;Han, Joon Kil;Kim, Seong Hwan;Lee, Ho Jung
    • Journal of Gastric Cancer
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    • 제16권2호
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    • pp.120-124
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    • 2016
  • Primary squamous cell carcinoma (SCC) of the stomach is a very rare disease. However, the pathogenesis, clinical characteristics, and prognosis of gastric SCC are controversial and remain to be elucidated. Herein, we report a case of primary gastric SCC of the remnant stomach after subtotal gastrectomy. A 65-year-old man was admitted to our hospital due to epigastric discomfort and dizziness. He had undergone subtotal gastrectomy 40 years previously for gastric ulcer perforation. Endoscopy revealed a normal esophagus and a large mass in the remnant stomach. Abdominal computed tomography revealed enhanced wall thickening of the anastomotic site and suspected metachronous gastric cancer. Endoscopic biopsy revealed SCC. Total gastrectomy was performed with Roux-en-Y esophagojejunostomy. A 10-cm tumor was located at the remnant stomach just proximal to the previous area of anastomosis. Pathologic examination showed well-differentiated SCC extended into the subserosa without lymph node involvement (T3N0M0). The patient received adjuvant systemic chemotherapy with 6 cycles of 5-FU and cisplatin regimen, and he is still alive at the 54-month follow-up. According to the treatment principles of gastric cancer, early detection and radical surgical resection can improve the prognosis.

비세균성 신염환자에서 신장내 $^{67}Ga-Citrate$ 흡수에 관한 연구 (Renal Localization of Ga-67 Citrate in Noninfectious Nephritis)

  • 이강욱;정민수;이순구;김삼용;신영태;노흥규
    • 대한핵의학회지
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    • 제26권2호
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    • pp.318-326
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    • 1992
  • Ga-67 citrate scan has been requested for detection or follow-up of inflammatory or neoplastic disease. Visualization of Ga-67 citrate in the kidneys at 48 and 72 hr post injection is usually interpreted as evidence of renal pathology. But precise mechanisms of abnormal Ga-67 uptake in kidneys were unknown. We undertook a study to determine the clinical value of Ga-67 citrate imaging of the kidneys in 68 patients with primary or secondary nephropathy confirmed by renal biopsy and 66 control patients without renal disease. Renal uptake in 48 to 72 hr images was graded as follows: Grade 0=back-ground activity:1=faint uptake greater than background;2=definite uptake, but less than lumbar vertebrae; 3=same uptake as lumbar vertebrae, but less than liver; 4=same or higher uptake than liver. The results were as follows. 1) 42 of 65 (62%) patients with noninfectious nephritis showed grade 2 or higher Ga-67 renal uptake but only 10 percent of control patients showed similar uptake. 2) In 14 patients with systemic lupus erythematosus, 8 of 9 (89%) patients with lupus nephritis exhibited marked renal uptake 3) 36 of 41 patients (88%) with combined nephrotic syndrome showed Grade 2 or higher renal uptake. 4) Renal Ga-67 uptake was correlated with clinical severity of nephrotic syndrome determined by serum albumin level, 24 hr urine protein excretion and serum lipid levels. 5) After complete remission of nephrotic syndrome, renal uptake in all 8 patients who were initially Grade 3 or 4, decreased to Grade 1 or 0. In conclusion, we think that the mechanism of renal Ga-67 uptake in nephrotic syndrome might be related to the pathogenesis of nephrotic syndrome. In systemic lupus erythematosus, Ga-67 citrate scan is useful in predicting renal involvement.

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미분화 갑상선암의 치료 (Treatment of Anaplastic Thyroid Cancer)

  • 장항석;윤종호;정웅윤;이미경;박정수
    • 대한두경부종양학회지
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    • 제14권2호
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    • pp.220-227
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    • 1998
  • The clinical and pathological features of 35 cases of anaplastic thyroid cancer were studied. These tumors occurred in 12 men and 23 women ranging in age from 19 to 83 years(mean age; 61.7 years). A rapidly enlarging thyroid mass was the most common presentation. The duration of the presence of mass varied from 20 days to 12 months with an average of 2.7 months. Systemic metastasis at the time of initial examination was found in 14 patients(40.0%) and the lung was the most common site of involvement. The overall rate of distant metastasis was about 65.7%. The tumors were subdivided morphologically into giant cell type of 10 cases, spindle cell type of 7 cases, epidermoid cell type of 1 cases, and mixed giant cell and spindle cell type of 5 cases. The mean survival period of 6 among 35 patients who had biopsy alone was 1.4 months. The 22 patients underwent the incomplete combined treatment modalities (palliative surgery with or without chemotherpy or radiation therapy) survived for a mean period of 3.0 months, among them, 7 patients who had surgery combined with chemotherapy and radiation therapy showed mean survival period of 3.7 months. The mean survival of 7 patients who had complete combined treatment modality(curative surgery combined with chemotherapy and hyperfractionated radiation therapy) was 6.6 months, only one patient survived for 21 months and one patient has been alive for 1 month after operation, and the others survived for a mean period of 4.8 months. So far, as of July 31, 1998, 34 patients among 35 were died(one has been survived for 1 month) despite the various treatment modalities, and the main cause of death were failure of local control and systemic metastasis. None of the various treatment modalities gave consistently favourable results. However, a combination of surgery, radiation therapy and chemotherapy seemed to have a slight positive effect on survival. Furthermore, the aggressive treatment modalities will be indicated only in the early diagnosed and minimal cases.

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Clinico-Pathologic Subtypes of Breast Cancer Primary Tumors Are Related to Prognosis after Recurrence

  • Sanchez, Cesar;Camus, Mauricio;Medina, Lidia;Oddo, David;Artigas, Rocio;Sepulveda, Alejandra Perez;Domainguez, Francisco;Razmilic, Dravna;Navarro, Maria Elena;Galindo, Hector;Acevedo, Francisco
    • Asian Pacific Journal of Cancer Prevention
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    • 제17권12호
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    • pp.5081-5086
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    • 2016
  • Background: Pathological factors, based mainly on immunohistochemistry (IHC) and histological differentiation, are mostly used to differentiate breast cancer (BC) subtypes. Our present aim was to describe the characteristics and survival of a relapsing BC patient cohort based on clinico-pathologic subtypes determined for the primary tumors. Methods: We used a clinico- pathological definition of BC subtypes based on histological grade (HG), estrogen receptor (ER), progesterone receptor (PgR),and epidermal growth factor receptor type 2 (HER2) expression assessed by IHC. We determined variables associated with loco-regional recurrence (LRR), second primaries (SP), systemic recurrence (SR) and post-recurrence survival (PRS). Results: Out of 1,702 patients, 240 (14%) had an event defined as recurrence. Those with recurrent disease were significantly younger than those without,and were initially diagnosed at more advanced stages, with larger tumors, greater lymph nodal involvement and higher HG. With a median follow up of 61 months (1-250), 4.6% of patients without recurrence and 56.6% of patients with an event defined as recurrence had died. The median PRS for the LRR group was 77 months; 75 months for those who developed a SP and 22 months for patients with an SR (p <0.0001). In SR cases, the median PRS was shorter for ER- tumors than for ER+ tumors (15 vs. 26 months, respectively; p = 0.0019, HR 0.44; CI: 0.25-0.44). Conclusions: Subtype, defined through classic histopathologic parameters determined for primary tumors, was found to eb related to type of recurrence and also to prognosis after relapse.

연소성 류마티스 관절염의 임상적 고찰 (Clinical observations of juvenile rheumatoid arthritis)

  • 이주훈;유정민;박영서
    • Clinical and Experimental Pediatrics
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    • 제49권4호
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    • pp.424-430
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    • 2006
  • 목 적 : JRA는 소아에서 가장 흔한 결체 조직 질환 중의 하나이고 장, 단기적인 신체장애를 유발하는 중요한 원인이 된다. 저자들은 JRA 환아들의 질병 양상과 경과를 알아보기 위하여 본 연구를 시행하였다. 방 법 : 1990년 8월부터 2004년 11월까지 서울아산병원 소아과를 내원한 59명의 JRA 환아를 대상으로 하였다. 성별, 연령, 유형, 침범 관절, 관절 외 소견, 검사 및 방사선 소견, 치료, 경과 등에 대하여 후향적으로 고찰하였다. 결 과 : 소수 관절형은 32.2%, 다수 관절형은 30.5%, 전신형은 37.3%였다. 남녀비는 1.7 : 1이었으며 평균 발병 연령은 $9.3{\pm}3.7$(1.3-15.9)세이었다. 가장 흔히 침범된 관절은 무릎과 발목, 팔목이었다. 관절 외 소견을 살펴보면 발열, 발진, 근육통, 림프절 비대 등이 있었다. 검사 소견을 살펴보면 백혈구증가증, 빈혈, 혈소판증가증, ESR 상승, CRP 상승 등의 소견을 보였다. 류마토이드 인자, 항핵항체 양성률은 각각 5.3%, 18.0%이었다. 비스테로이드성 소염제(NSAID)가 가장 많이 투여되었으며, 메토트렉세이트 또는 스테로이드를 함께 투여했던 경우가 27.1%였다. 88.1%의 환아에서 장애 후유증 없이 완치되었으며 한 명의 환아에서만 기능성 상태 IV의 장애가 있었다. 폐침범이 동반되었던 한 명의 환아가 사망하였다. 결 론 : 본 연구에서는 균등한 유형별 분포, 남아에서 호발하는 양상, 늦은 발병 연령, 낮은 홍채모양체염 발병률, 그리고 낮은 ANA 양성률을 보였는데 이러한 소견들은 한국에서의 JRA의 소견이며 서양에서의 보고와는 상이한 결과들이다. JRA가 민족과 지역에 따라서 서로 다른 발병양상을 보인다는 점을 시사한다고 생각된다. 앞으로 더 많은 수의 환자들을 대상으로 하는 다기관 협동 연구 및 역학조사가 필요할 것으로 생각된다.