• Title/Summary/Keyword: interlacing

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Overlay Network망에서의 실시간 멀티플레이어 P2P게임 시스템 (A P2P Real-time Game System for Multiplayer on Overlay Network)

  • 정미숙;박규석
    • 한국멀티미디어학회논문지
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    • 제13권1호
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    • pp.38-46
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    • 2010
  • P2P온라인 게임 시스템에서 대규모 사용자의 동시 접속을 수용할 수 있는 안전한 게임 운영 시스템이 필수적이다. 본 논문에서 제안하는 P2P 온라인 게임 시스템은 RS(Region Sever)들의 재구성 및 RS간의 숭호 정보 교환을 통해 한 영역에 플레이어가 집중되는 현상을 피하여 대규모 플레이어를 수용할 수 있으며, 안전한 게임을 운영할 수 있다. 또한 모니터링 서버의 광역 버퍼(Global Zone Buffer)를 이용한 부하분산으로 타임스탬프 시간 내의 게임 동기화가 가능하며고 미들웨어를 단위 영역별로 관리하여 게임 월드의 크기에 관계없이 수행 가능하다. 따라서, 서버 추가 문제의 해결 및 메시지 전송의 안정성을 확보할 수 있다. 또한, 시뮬레이션을 통하여 제안 시스템에 대한 효율성을 입증한다.

말초신경초 종양의 특징을 지닌 개 신경종의 조직병리학적 및 면역조직화학적 진단 (Canine nervous-tissue tumors with features of peripheral nerve sheath tumor: histopathological and immunohistochemical findings)

  • 이선규;이재하;한정희
    • 한국동물위생학회지
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    • 제41권1호
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    • pp.57-61
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    • 2018
  • Canine peripheral nerve sheath tumors (PNSTs) are spindle cell tumors that arise from Schwann cells, perineural cells, fibroblasts or all of them. Based on the morphology and biologic behavior, PNSTs are divided into benign PNST (BPNST) and malignant PNST (MPNST) forms. The aim of this study is to diagnose the two cases of neoplastic tissue samples with features of PNSTs by the histopathology and immunohistochemistry. The study was performed using two specimens from small animal clinic. The first case, A was a mass, 3~4 cm in diameter, extruded from vaginal mucosa of 10-year-old spayed female mixed-breed dog. And the second case, B was a subcutaneous mass, 1.5 cm in diameter, which is originated from right hind leg of 9-year-old castrated male mixed-breed dog. Two cases were stained with hematoxylin and eosin (H&E) for histopathological examination. And also immunohistochemistry (IHC) was performed by the avidin-biotin peroxidase complex (ABC) method with antibodies specific for the following proteins: S-100 protein, smooth muscle actin (SMA) and epidermal growth factor receptor (EGFR). In results, Antoni B schwannoma pattern characterized by pleomorphic, round and fusiform polygonal cells was seen in A. In B, Antoni A pattern, densely packed spindle cells arranged in interlacing bundles was seen in addition to Antoni B pattern. In IHC, cytoplasms of neoplastic cells were diffusely labeled for S-100 expression in A and B. For SMA, both A and B show negative expression. And for EGFR, A shows negative expression but B shows partially positive expression in areas of Antoni B schwannoma pattern. The histopathologic features of two cases coupled with the S-100 immunoreactivity led to a diagnosis of PNST. For SMA, both A and B show negative expression. The diagnosis of A will be a BPNST with the negative result and B will be a MPNST with the positive result for EGFR.

개에서 국소형과 범발성형 조직구육종 2예 (Localized and disseminated histiocytic sarcoma in two dogs)

  • 권효정;박미선;오상연;지향;조두연;김대용
    • 대한수의학회지
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    • 제45권3호
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    • pp.369-373
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    • 2005
  • A male mixed breed dog with unknown age (case 1) and 5-year-old female golden retriever (case 2) were admitted to the Department of Veterinary Pathology at College of Veterinary Medicine, Seoul National University after sudden death. At necropsy, stifle region of case 1 was replaced by coalescing firm tan nodules approximately 1-3 cm in diameter. Neoplastic nodules were also presented in the lung. In case 2, the spleen was enlarged 3-5 times its normal size and numerous firm tan nodules were noted in the kidney, pericardium, diaphragm and lymph nodes. Histopathologically, the neoplastic masses of case 1 consisted of plump spindle cells having abundant cytoplasm and indistinct cell borders that formed interlacing bundle. In case 2, the masses were consisted of round to polygonal cells with abundant eosinophilic cytoplasm and eccentric nuclei. Numerous multinucleated giant cells containing nuclei of various sizes were noted. Immunohistochemically, neoplastic cells of all two cases stained intensely with vimentin and lysozyme. Based on the gross and light microscopic findings together with immunohistochemistry, both cases were diagnosed as localized histiocytic sarcoma with pulmonary metastasis and disseminated histiocytic sarcoma, respectively.

다중연산구조기반의 고밀도 성능향상을 위한 움직임추정의 디인터레이싱 방법 (Deinterlacing Method for improving Motion Estimator based on multi arithmetic Architecture)

  • 이강환
    • 대한전자공학회논문지SP
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    • 제44권1호
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    • pp.49-55
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    • 2007
  • 본 논문에서는 필드/프레임의 공간적, 시간적 움직임 특성을 활용한 디인터레이스드 기법을 이용해 재구성된 영상프레임으로부터 넓은 탐색영역에서의 움직임추정이 가능한 이중연산구조 기반의 다해상도 계층적 움직임 추정 방식(multi- resolution hierarchical motion estimation, MHME)의 효율적인 다중연산구조 기반의 움직임 추정을 제안한다. 공간적, 시간적 움직임 특성으로부터 디인터레이스드 기법을 적용하여 재구성된 영상프레임으로부터는 계층적 움직임 추정방식을 적용하여 빠른 움직임 영역에서도 화질의 열화가 거의 없는 다해상도 계층적 움직임 추정(MHME) 영상처리를 구현하였고, 비교적 높은 PSNR을 얻을 수 있었다. 다양한 모드 M=2 또는 M=3의 여러 가지 모의실험을 통해 제안된 구조가 전역탐색 블록정합 알고리듬(Full-search Block Matching Algorithm, FBMA)에 대하여 예측성능에 있어 최고 1.49dB(CAR), 최저0.421dB(Mobile & Calendar)의 모의실험결과 평균 -0.7dB 정도의 미소한 평균 PSNR 저하를 나타내었다. 이의 구현을 위해 제안된 전역/후역 탐색방식의 연산처리방식은 하나의 처리기소자(Processor Element, PE)에 이중연산처리기(DAPE) 구조를 채택하여 제한된 PE로부터 넓은 탐색영역에서의 움직임 추정이 가능한 전역/후역 탐색방식(Foreground & Background Search Algorithm, FBSA)의 비트 처리열 탐색 알고리듬을 제안 적용하여 움직임추정 연산의 성능을 구조적으로 향상시키는 다중프로세서 어레이 구조(Multiple Processor Array Unit, MPAU)를 개발 제안하였다.

성인에서 발생한 중배엽성 신종의 폐전이 1예 (A Case of Lung Metastasis of Mesoblastic Nephroma in Adulthood)

  • 문진욱;김길동;신동환;한창훈;정재호;박무석;정상윤;이재혁;김영삼;김세규;김성규;장준
    • Tuberculosis and Respiratory Diseases
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    • 제55권4호
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    • pp.402-407
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    • 2003
  • 저자 등은 성인에서 드물며, 또한 국내에서 원격전이를 일으킨 예가 보고된 바 없는 중배엽성 신종이 35세 여자 환자에서 발생하여 신적출술 7년 후 폐전이로 하나의 큰 종괴를 형성한 증례를 경험하였기에 문헌 고찰과 함께 보고하는 바이다.

이하부에 발생한 침습성 섬유종증이 하악체에 침범한 증례 보고 (A CASE OF AGGRESSIVE FIBROMATOSIS INVADED MANDIBULAR BODY ON THE PAROTID REGION)

  • 김영조;이동근;엄인웅;민승기;정창주;김은철
    • Maxillofacial Plastic and Reconstructive Surgery
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    • 제16권2호
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    • pp.186-195
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    • 1994
  • Fibromatosis is benign fibroblastic proliferative lesion with abundant collagenous neo-formation located principally in the abdominal wall and in the upper and lower extremities (Masson & Soule, 1966). Wilkins and Waldron, in 1975, suggested that the title aggressive fibromatosis was a more appropriate term, reflecting the invasive characteristics of the disease. Synonyms listed were extra-abdominal desmoid, juvenile fibromatosis, aggressive infantile fibromatosis and congenital fibrosarcoma. A total of 12% of all fibromatosis arise in head and neck. Fibromatosis of the oral cavity is uncommon and is even more rare when in involve the mandibule. It is a locally aggressive fibrous tissue tumor, generally does not metastasize, but may cause considerable morbility and even death due to local infiltration. The degree of microscopic cellularity is variable, not only from tumor to tumor but also from area to area in the same tumor. Some tumors present with proliferation of mature fibroblasts and a dominating collagenous component : others may show a lack of the tumor in both types. The common histologic denominator appears to be cellular interlacing bundles of elongated fibroblasts, showing little or no mitotic activity and no pleomorphism. Mitosis are not a consistent index of malignancy when found in younger age groups. Fibromatosis still posses difficult problems of diagnosis and treatment. It is frequently recurrent and infliltrates neighbouring tissues. These lesion infliltrate widely and replace muscle, fat, and even bone with fibrous tissue of varying cellularity. Lesion representing fibromatosis in the oral cavity must be carefully evaulated by both surgeon and pathologists to ensure proper diagnosis and treatment planning. When these lesions involve bone, surgeon must be aware of the lesion's potential to perforate the cortex and expand while remaining hidden from the surgeon's view. Careful and precise clinical correlation with histologic appearance is essential to preclude misdiagnosis of fibrosarcoma yet provide surgical treatment plan that provides adequate local excision and long-term follow up. As regards cause, little is known. It is attributed to trauma or alteration in the sex hormone(Carlos, et al, 1986). Clinially, the lesion is reported to be not painful in most cases, but capable of rapid growth. The treatment is essentially surgical excision with wide margin of adjacent uninvolved tissue. Radiotherapy, hormone treatment or chemotherapy are of no use (WIkins et al, 1975 ; Majumudar and Winiarkl, 1978). We report a case of aggressive fibromatosis of 15-year-old with a lesion in the soft tissue of the parotid area that invaded the underlying bone of the mandibular body.

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