192 research outputs found

    Characteristics of repair tissue in second-look and third-look biopsies from patients treated with engineered cartilage: relationship to symptomatology and time after implantation

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    INTRODUCTION: The present study established characteristics of tissue regrowth in patients suffering knee lesions treated with grafts of autologous chondrocytes grown on three-dimensional hyaluronic acid biomaterials. METHODS: This multicentred study involved a second-look arthroscopy/biopsy, 5 to 33 months post implant (n = 63). Seven patients allowed a third-look biopsy, three of which were performed 18 months post implant. Characteristics of tissues were histologically and histochemically evaluated. The remaining bone stubs were evaluated for cartilage/bone integration. For data analysis, biopsies were further divided into those obtained from postoperative symptomatic patients (n = 41) or from asymptomatic patients (n = 22). RESULTS: The percentage of hyaline regenerated tissues was significantly greater in biopsies obtained after, versus within, 18 months of implantation. Differences were also observed between symptomatic and asymptomatic patients: reparative tissues taken from symptomatic patients 18 months after grafting were mainly fibrocartilage or mixed (hyaline-fibrocartilage) tissue, while tissues taken from asymptomatic patients were hyaline cartilage in 83% of biopsies. In a small group of asymptomatic patients (n = 3), second-look and third-look biopsies taken 18 months after surgery confirmed maturation of the newly formed tissue over time. Cartilage maturation occurred from the inner regions of the graft, in contact with subchondral bone, towards the periphery of the implant. CONCLUSIONS: The study indicates that, in asymptomatic patients after chondrocyte implantation, regenerated tissue undergoes a process of maturation that in the majority of cases takes longer than 18 months for completion and leads to hyaline tissue and not fibrous cartilage. Persistence of symptoms might reflect the presence of a nonhyaline cartilage repair tissue

    The effects of transurethral resection and cystoprostatectomy on dissemination of epithelial cells in the circulation of patients with bladder cancer

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    This study was undertaken to evaluate the risk of haematogenous dissemination of epithelial cells induced by endoscopic resection and/or cystoprostatectomy for transitional cell carcinoma of the bladder. Thirty-three patients were studied. Thirty-one had different stages and grades of bladder cancer and two patients had benign bladder conditions. Twenty-five cancer patients required transurethral resection of their bladder tumour. Of those, 20 had superficial disease (pTaG1–G2: n = 19; pT1G2: n = 1) and five had muscle invasive tumours (pT2G3: n = 2; pT3aG3: n = 1; pT4G3: n = 2). Five patients underwent radical cystoprostatectomy for muscle invasive cancers (pT2G3: n = 3; pT3bG3: n = 1; pT4G3: n = 1) and one man received chemotherapy for metastatic disease. Venous blood (10 ml) was obtained from the antecubital fossa in each patient, before and 1–2 h after completion of surgery, and prior to treatment in the metastatic patient. An indirect immunocytochemical technique was used to detect circulating epithelial cells after centrifugation on Ficoll gradient and fixation of mononuclear cells on slides, using a monoclonal antibody directed against three cytokeratins: CK8, CK18 and CK19. Circulating epithelial cells were detected only in the patient with metastatic disease. None of the other patients had evidence of epithelial circulating cells before or after surgery. The results suggest that irrespective of disease stage and grade, neither endoscopic nor open bladder surgery leads to detectable dissemination of urothelial cells in the peripheral circulation. These procedures are therefore unlikely to increase the risk of progression and metastasis in transitional cell carcinoma of the bladder. © 1999 Cancer Research Campaig

    CNN-based multi-modal camera model identification on video sequences

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    Identifying the source camera of images and videos has gained significant importance in multimedia forensics. It allows tracing back data to their creator, thus enabling to solve copyright infringement cases and expose the authors of hideous crimes. In this paper, we focus on the problem of camera model identification for video sequences, that is, given a video under analysis, detecting the camera model used for its acquisition. To this purpose, we develop two different CNN-based camera model identification methods, working in a novel multi-modal scenario. Differently from mono-modal methods, which use only the visual or audio information from the investigated video to tackle the identification task, the proposed multi-modal methods jointly exploit audio and visual information. We test our proposed methodologies on the well-known Vision dataset, which collects almost 2000 video sequences belonging to different devices. Experiments are performed, considering native videos directly acquired by their acquisition devices and videos uploaded on social media platforms, such as YouTube and WhatsApp. The achieved results show that the proposed multi-modal approaches significantly outperform their mono-modal counterparts, representing a valuable strategy for the tackled problem and opening future research to even more challenging scenarios

    Problems in determining A2B group specific properties in blood stains

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    Amino acid content in fresh sperm and sperm stains

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    Seminal fluid was studied biochemically for sperm identification in stains. The qualitative and quantitative distribution of amino acids in samples of fresh sperm has been analyzed. These findings were compared to the results of a similar study of fresh samples and stains of urine, saliva, vaginal fluor, and sweat. The results obtained show a specific and relatively constant level of amino acids in each of five biological liquids. There was no significant variation in results between fresh samples and stains
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