• 제목/요약/키워드: Cystic lesions

검색결과 282건 처리시간 0.022초

항-표피성장인자수용체 단클론항체와 DNA 토포이소머라제 억제제에 의한 마우스 모델에서의 타액선 선낭암종 성장 억제 (Anti-epidermal growth factor receptor (EGFR) monoclonal antibody and DNA topoisomerase inhibitor reduce growth of salivary adenoid cystic carcinoma in a murine model)

  • 박영욱;이희수
    • Journal of the Korean Association of Oral and Maxillofacial Surgeons
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    • 제36권3호
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    • pp.177-185
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    • 2010
  • Introduction: Epidermal growth factor receptor (EGFR) is expressed in human epithelial tumors including salivary cancers, and known to be correlated with tumor progression and poor clinical courses in some epithelial tumors. In this study, we determined the therapeutic effect of the anti-EGFR monoclonal antibody Erbitux (C225, cetuximab) in combination with the DNA topoisomerase I inhibitor irinotecan (CPT-11) on human salivary adenoid cystic carcinoma (SACC) cells growing in nude mice. Materials and Methods: At first, immunocytochemical analysis for the expression of EGFR and phosphorylated EGFR (pEGFR) on a human salivary ACC cell line (ACC3). To determine the in vivo effects of Erbitux and CPT-11, nude mice with orthotopic parotid tumors were randomized to receive intraperitoneal Erbitux (1 mg) two times per week, intraperitoneal Irinotecan (50 mg/kg) once per week, Erbitux plus CPT-11, or placebo. (control) Tumor volume and weight were measured. And mechanisms of in vivo activity of Erbitux and/or CPT-11 were determined by immunohistochemical/ immunofluorescent analyses. Results: Immunocytochemical staining of ACC3 demonstrated that EGFR was expressed and phosphorylated. CPT-11 inhibited ACC tumor growth in nude mice. Tumors of mice treated with CPT-11 and CPT-11 plus Erbitux exhibited increased tumor cell apoptosis and decreased microvessel density, which correlated with a decrease in the tumor volume in nude mice. But, CPT-11 seems not to be synergistic with Erbitux in our ACC3 model system. Conclusion: These results suggest that anti-EGFR monoclonal antibody and the DNA topoisomerase I inhibitor will be effective in the treatment of recurred or metastatic lesions of salivary ACC.

슈반세포종 23예의 세침흡인 세포검사에 대한 세포소견 (Cytologic Findings of Fine Needle Aspiration Biopsy of 23 Schwannomas)

  • 장선희;주미;김한성
    • 대한세포병리학회지
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    • 제19권1호
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    • pp.41-46
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    • 2008
  • In an attempt to better define the cytologic characteristics of schwannomas, we have reviewed aspirates and corresponding histologic sections from 23 schwannomas. Of this number, the original cytologic diagnoses were: schwannoma in 14 cases (61%), benign soft tissue tumor in 2 cases (9%), and insufficient specimen in 7 cases (30%). The cytologic findings common to all cases of schwannoma included fragments of tightly cohesive fascicles with variable cellularity and corresponding Antoni type A area. The Antoni type B area, consisting of scattered spindle cells and some histiocytes and lymphocytes against a myxoid background, was seen in 14 cases. Fibrillary stroma was seen in 12 cases. The tumor cells had spindle- or ovalshaped nuclei, with pointed ends and indistinct cell borders. Nuclear palisading was seen in 10 cases, and distinctive Verocay bodies were seen in 5 cases. In ancient schwannomas, there were no Verocay bodies. Most schwannomas have distinct cytomorphologic features that allow correct diagnosis. The major problem with fine needle aspiration cytology of these tumors is the high frequency of poor cellularity, particularly in lesions with cystic degeneration. Of 7 cases with insufficient specimen, 4 showed marked cystic changes and 1 showed marked hyaline changes on histologic sections. In conclusion, we believe that if cytopathologist reminds the situation such as cystic degeneration or hyaline degeneration, the correct diagnosis of the schwannoma will be easily made.

피하 흉터 조직에서 발견된 후천성 유피낭종 (Acquired Dermoid Cysts within Subcutaneous Scar Tissue)

  • 김형진;범진식;변재경;김양우
    • Archives of Plastic Surgery
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    • 제34권4호
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    • pp.508-511
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    • 2007
  • Purpose: Dermoid cysts are almost always caused by congenital events. The most widely accepted pathogenesis is that the cysts are dysembryogenetic lesions that arise from ectodermic elements entrapped during the midline fusion. We report a rare case of dermoid cyst, which occurred not congenitally but newly in the subcutaneous scar tissue secondary to trauma. Methods: A 26-year-old man had a deep submental laceration caused by a car accident and got a primary wound closure 16 months ago. There were 18 cm-long submental hypertrophic scar and newly developed palpable masses inside the subcutaneous layer at the center of the scar. Initial impression was an epidermal cyst or a thyroglossal duct cyst. Ultrasonographic finding showed two cystic masses inside the scars at the submental area, but impressed dermoid cysts. The cystic masses were completely removed with W-plasty and histological examination were followed. Results: The histological diagnosis was dermoid cysts which were mainly composed of keratotic squamous epithelium in their inner surface linings and numerous skin appendages such as sebaceous glands, sweat glands, and hair follicles in their cystic lumens histopathologically. During the follow-up period of 25 months, there was no recurrence of any subcutaneous mass in the site of scar. Conclusion: We report a very unusual case of dermoid cysts developed by an acquired cause, considering that the accidental inclusion of deep skin elements caused by a trauma can be a critical origin of dermoid cysts.

간질성 및 다낭성 폐질환이 동반된 쇼그렌 증후군 1례 (A Case of Sj$\ddot{o}$gren's Syndrome with Interstitial Lung Disease and Multiple Cystic Lung Disease)

  • 장대용;신병철;정기영;김종오;양종태;주유철;이승일
    • Tuberculosis and Respiratory Diseases
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    • 제51권6호
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    • pp.597-602
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    • 2001
  • A 47-years-old woman presented with a 2-month history of a dry mouth and dry cough. The patient had been taking medication for Sj$\ddot{o}$gren's syndrome for approximately 7 years. The chest radiography showed multiple cystic lesions and a hazy density in both lower lung fields. The HRCT showed a diffuse ground glass like appearance and multiple variable sized cystic lesions in both lung fields. After medication, the symptoms were aggravated. Bronchoscopy was preformed with a transbronchial lung biopsy. The biopsies showed an infiltration of lymphocytes, neutrophils, monocytes and histiocytes through the interstitial space of the alveola and a widening of the alveolar septa. However, the histological findings of the cysts were not obtained. Sj$\ddot{o}$gren's syndrome is a slowly progressive inflammatory autoimmune disease, which is characterized by lymphocyte mediated destruction of the exocrine glands, with pulmonary involvement in approximately 19-65%, High-resolution CT is a sensitive technique for assessing the pulmonary involvement in patients with Sj$\ddot{o}$gren's syndrome. Although a lung biopsy is not always necessary for establishing a diagnosis of an interstitial lung disease in Sj$\ddot{o}$gren's syndrome. A lung biopsy may reveal a wide spectrum of changes ranging from a mild inflammatory response to end stage fibrosis with honeycombing. Because of the predominantly peribronchiolar inflammatory infiltration and inspissated secretions the cysts were suspected to have been formed by the ball-valve phenomen. However, no definite evidence was obtained.

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초음파 진단기의 설정 파라미터가 영상의 질에 미치는 효과 (Effects of Ultrasonic Scanner Setting Parameters on the Quality of Ultrasonic Images)

  • 양정화;이경성;강관석;팽동국;최민주
    • 한국음향학회지
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    • 제27권2호
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    • pp.57-65
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    • 2008
  • 초음파 진단기의 설정은 영상의 질에 영향을 준다. sonographer는 최적의 영상을 얻기 위해 초음파 영상의 질에 영향을 주는 설정 변수에 대한 효과를 이해해야 한다. 본 연구에서는 4가지 대표적인 영상 조절 변수 즉 TGC (Time Gain Control), 이득 (Gain), 주파수 (Frequency), DR (Dynamic Range)를 고려하였다. 초음파 영상의 질은 LCS (Law Contrast Sensitivity) 관점에서 정량적으로 비친 평가하였다. 실험은 임상용 초음파 진단기 (SA-9000 PRIME, Medison, Korea)를 사용하여 초음파 평가 팬텀 (539, ATS, USA)의 LCS 타겟을 영상화하였다. 영상 조절 변수의 설정을 변화하면서, 각 설정에 대한, 6개의 LCS 영상 (+15 dB, +C dB, +3 dB, -3 dB, -6 dB, -15 dB)을 취득하고, 영상에 대한 LCS픽셀 값을 계산하였다. 실험결과 TGC가 최대, Gain은 중간에서 최대사이, 주파수가 Pen모드, DR이 40-66 dB일 때 타겟 영상 (LCS)의 평균 픽셀 값이 높았다. 모든 타겟 영상에서 DR이 40 dB일 때에 LCS가 좋은 영상을 얻었다. 본 결과는 임상에서 잘 발견되는 solid lesion (+15, +6, +3 dB 타겟과 유사) 또는 cystic lesion (-15, -6, -3 dB 타겟과 비슷)이 있는 mass 평가 시 적절한 영상조절 변수 설정에 유용한 정보를 제공할 것으로 기대된다.

타액선 질환에 대한 세침흡인세포검사의 유용성 (Efficacy of Fine Needle Aspiration Cytology of Salivary Gland Diseases)

  • 박민현;이승신;최병윤;김인상;최승호;고태용;김광현;성명훈
    • 대한두경부종양학회지
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    • 제16권1호
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    • pp.42-45
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    • 2000
  • Background and Objectives: To review efficacy of the fine-needle aspiration cytology(FNAC) in patients with salivary glands lesions. Materials and Methods: From January 1994 through June 1999, FNACs and surgical biopsies were carried out on 109 patients with salivary gland diseases. The medical records were reviewed retrospectively. Benign tumor was found in 81 patients, and malignant tumor was in 19 patients. Nine patients had inflammatory lesion. Results: In 6 of 109 cases the aspiration was inadequate. Of the remaining 103 patients, FNAC correctly diagnosed 87 lesions(84.5%). For benign tumor lesions, the accuracy was 91%(71/78), and for malignant lesions 55.6%(10/18). The accuracy for inflammatory lesions was 85.7%(6/7). Regarding the capacity to discriminate between neoplastic and nonneoplastic lesions, sensitivity, specificity and total diagnostic accuracy were 99%, 85.7% and 84.5% respectively. Regarding the capacity to discriminate between malignant and benign tumors, sensitivity and specificity were 55.6% and 97.4% respectively. FNACs misdiagnosed malignant tumors as benign lesions in eight patients, in which three were with adenoid cystic carcinomas. Carcinoma ex pleomorphic adenoma, malignant lymphoma and mucoepidermoid carcinoma 'were others. Conclusion: FNAC showed high accuracy to diagnose benign lesions in salivary gland diseases. But the accuracy was rather low for malignant lesions. If a salivary gland lesion was suspected for malignant tumor, other diagnostic methods such as tissue biopsy should be seriously considered.

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소아의 제 2 새궁 기형의 임상적 고찰 (Clinical Analysis of Second Branchial Cleft Anomalies in Children)

  • 이준우;김수홍;김현영;박귀원;정성은
    • Advances in pediatric surgery
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    • 제17권2호
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    • pp.162-169
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    • 2011
  • Branchial cleft anomalies are the second most common head and neck congenital lesions seen in children. Amongst the branchial cleft malformations, second cleft lesions account for 95 % of the branchial anomalies. This article analyzes all the cases of second branchial cleft anomalies operated on at Seoul National University Hospital from September 1995 to February 2011. We analyzed sex, age, symptom and sign, accompanied anomaly, diagnosis, treatment, pathologic report and outcome via retrospective review of medical records. In this series, we had 61 patients (27 female and 34 male). The mean age at the time of operation was 38 months. 31 lesions were on the right, 20 were on the left and 10 were bilateral. The most frequent chief complaints at presentation were non-tender mass and cervical opening without any discharge. According to anatomic type, 29 patients had branchial cleft sinuses, 14 had cysts, 14 had fistulas and 4 had skin tags. Complete excision was attempted if possible and antibiotics challenged when infection was suspected. Complete excision was achieved in 96.7 % of cases. Incision and drainage was done in 2 cases due to severe inflammation, and both recurred. Postoperative complications included wound infection in 2 cases. Microscopic examonation revealed squamous epithelium in 90.2 % and squamous metaplasia in one case in the branchial cleft cyst wall. In summary, second branchial anomaly is found more frequently on right side of neck. Fistulas are diagnosed earlier than cystic forms. Most cases could be diagnosed by physical examination. The definitive treatment is complete excision and sufficient antibiotics coverage for cases with inflammation. After drainage of infected lesions, follow up excision after 1 year might be beneficial for preventing recurrence.

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단순 방사선 상에서 발견할 수 없었던 거골 골연골 병변의 MRI 소견과 관절경 소견 (MRI and Arthroscopy of Osteochondral Lesion of the Talus which was not visible on Plasin Radiography)

  • 이우천;심재찬;최덕신
    • 대한족부족관절학회지
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    • 제6권2호
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    • pp.195-200
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    • 2002
  • Purpose: To investigate the MRI and arthroscopic findings of osteochondral lesion of the talus which looked normal on plane radiography. Materials and methods: We investigated the MRI and arthroscopic findings of seven osteochondral lesions in which there were no abnormal finding on plane radiography and no cystic changes on MRI. Average age was 31 years(range, 19-43 years). Arthroscopic findings were classified according to the Ferkel's criteria. Results: History of injury was reported in all cases and the average duration from injury to presentation was 4 years and 4 months. Low signal change in T1WI was found in 6 of 7 lesions, no signal change in 1 case. Low signal change in T2WI was found in 4, no signal change in 3. 6 STIR images were obtained. High signal change was found in 3, no signal change in 2 and intermediate signal change was in 1. Arthroscopic grading was A in 1, C in 1, D in 2 , E in 1 and F in 2. We could not find any correlation between the findings on MRI and arthroscopic examination. Conclusion: We suggest arthroscopic examination is needed for accurate diagnosis of the osteochondral lesions of the talus which looked normal on plane radiography, because they have various MRl findings and high likelihood of existence of unstable cartilage lesions.

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복부내 농양의 초음파 소견 (Ultrasonographic Features of Intra-abdominal Abscess)

  • 조길호;정경희;황미수;장재천;권굉보;민현식
    • Journal of Yeungnam Medical Science
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    • 제2권1호
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    • pp.87-93
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    • 1985
  • 1983년 5월부터 1985년 11월까지 영남대학교 의과대학 부속병원에서 복부농양을 의심하여 초음파검사를 시행후 확진된 48명의 환자에서 초음파소견을 분석하여 다음과 같은 결과를 얻었다. 1) 농양의 위치는 복강내 농양이 30예, 내장 농양이 13예, 후북막강농양이 5예였다. 2) 원인별로는 복강내 농양의 25예는 충수돌기염에 의하였고. 5예는 수술후 합병증으로 생겼다. 후복막강농양 5예는 전부 요근농양으로, 결핵성 및 화농성이 각각 2예, 후복막강에 위치한 충수돌기 염증이 1예였다. 내장농양은 12예가 간농양으로 이 중 9예는 화농성, 3예는 아메바성이었고 췌장염에 의한 췌장미부농양이 l예였다. 3) 형태는 총 48예중 26예(54%)에서 구형 또는 난원형이었으며, 특히 내장농양이 복강내 농양에 비해 구형 또는 난원형이 많았다. 4) 병변의 크기는 26예(54%)에서 5~10cm사이였으며, 내부echo는 33예(69%)에서 낭포성이었다.

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성인에서 진단된 선천성 낭포성 유선종 폐기형 6예 (Congenital Cystic Adenomatoid Malformation of Lung in Adults: Clinical, Pathologic and Radiologic Evaluation of Six Patients)

  • 박영진;정훈;박이내;최상봉;허진원;이혁표;염호기;최수전;구호석;이양행;최석진;정수진;이현경;김애란
    • Tuberculosis and Respiratory Diseases
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    • 제65권2호
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    • pp.110-115
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    • 2008
  • 연구배경: CCAM은 드문 하부 호흡기의 선천성 발달 기형으로 대부분은 생후 2년 내에 진단되는 것으로 보고되고 있다. 그리고 매우 드물게 성인이 되어서 호흡기 합병증이 생기거나 무증상인 채로 우연히 진단된 증례들이 보고되었다. 우리는 본원에서 수술을 통해 조직학적 소견으로 확진된 6명의 성인 CCAM 환자들을 기술하였고 이들의 임상적, 방사선학적 및 조직학적 특성을 분석하고자 하였다. 방 법: 2001년 8월부터 2007년 2월까지 본원에서 성인기에 수술을 통한 조직학적 소견으로 확진된 6명의 CCAM 환자를 확인하였다. 의무기록 검토를 통해 그들의 인구학적 및 임상적 특성, 흉부 방사선 자료 그리고 조직학적 특성을 후향적으로 분석하였다. 결 과: 6명의 CCAM 환자 중 4명이 여자였고 진단 당시의 평균 나이는 23.5세(범위 18~39세)였다. 내원 당시 주요 임상 양상은 하부 호흡기 감염, 객혈, 그리고 기흉이었다. 흉부 전산화 단층촬영을 보면 5명의 환자는 공기 액체층을 동반한 다발성 격막을 가진 낭종성 병변을 가지고 있었고 나머지 1명에서는 우상엽에 공기 액체층을 동반한 다발성 공동성 병변과 주위에 다발성 침윤성 병변을 가지고 있었다. 모든 환자는 폐엽 절제 수술을 받았는데 5명은 개흉술을 통한 폐엽 절제술을 그리고 1명은 흉강경을 이용한 폐엽 절제술을 시행 받았다. 조직학적 검사결과 Stocker씨 분류법에 따라 3명의 환자는 1형 그리고 나머지 3명은 2형으로 분류되었다. 모든 환자의 검체에서 동반된 악성 종양의 증거는 없었다. 결 론: CCAM이 하부 호흡기 감염, 기흉, 객혈 등의 다양한 호흡기 합병증과 악성화를 일으킬 가능성이 있고 수술적 치료와 연관된 합병증이 거의 없기 때문에 CCAM으로 의심되거나 확실치 않은 폐의 낭종성 혹은 공동성 병변이 있을 때 정확한 진단과 적절한 치료를 위해서 반드시 수술적 치료가 필요하다.