Andrés Sampedro
University of Oviedo
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Featured researches published by Andrés Sampedro.
The Journal of Pathology | 2001
Mario A. J. A. Hermsen; Marta Alonso Guervós; Gerrit A. Meijer; Jan P. A. Baak; Paul J. van Diest; César Álvarez Marcos; Andrés Sampedro
Squamous cell carcinomas of the head and neck generally exhibit complex karyotypes. To gain better knowledge of the changes in the subgroup of laryngeal and pharyngeal squamous cell carcinoma, chromosomal gains and losses were investigated in 42 predominantly late‐stage tumours, using comparative genomic hybridization. On average, 11.2 gains and 6.8 losses were found. Gains were detected in high frequencies at 1q, 3q, 5p, 7q, 8q, 11q13, 17q, and 18p, and losses at 3p, 4p, 5q, 11qter, and 18q. Neither the number nor the type of abnormalities, nor the occurrence of specific chromosome changes, was found to be related to DNA ploidy, tumour stage, or degree of differentiation. Apart from low‐level gains, many high‐level amplifications were identified, in particular 3q24‐qter (15 cases). Other regions recurrently involved were 11q13 (7 cases), 18p (5 cases), 18q11.2 (4 cases), and 8q23–24 and 11q14–22 (3 cases). Many of these amplified regions have not been reported before. Over half of all loci harbour genes coding for growth factors and growth factor receptors, suggesting an important role for such genes in squamous cell tumourigenesis and in the progression of late‐stage tumours. Copyright
Head and Neck-journal for The Sciences and Specialties of The Head and Neck | 1999
Luis Junquera; Damián Alonso; Andrés Sampedro; Florentino Fresno; Jose M. Albertos; Juan Sebastián López-Arranz
Primary surgery is the appropriate treatment for most pleomorphic adenomas of the salivary glands. However, no reliable criteria have been established to predict tumors with aggressive features.
Microbial Pathogenesis | 1990
J.R. de los Toyos; J. Vázquez; Andrés Sampedro; Carlos Hardisson
It is shown, for the first time, that Yersinia enterocolitica serotype O:3 is experimentally arthritogenic. Moreover, it is arthritogenic for the mouse, an optimal model for human yersiniosis. This arthritis can be induced by the oral route, the most common route in man. The pattern of joint disease closely parallels that of human reactive arthritis associated with this pathogen.
Analytical Cellular Pathology | 1998
Jose Antonio Alvarez-Riesgo; Andrés Sampedro; Radhamés Hernández; María Victoria Folgueras; Ana Salas-Bustamante; Antonio Cueto
Flow Cytometry (FC) has been incorporated into cancer research in relation to its prognostic value together with histological parameters and TNM stages. We have studied by means of FC the cell cycle of 132 samples from male patients with Squamous Cell Lung Carcinoma (SQCLC). All of the patients received curative surgery and the clinical follow-up was 60 months. The clinical and cytometric parameters were evaluated in order to predict the patients’ outcome. The presence of tumoural recurrence and the tumoural stage showed statistical significance associated with survival. The multivariant analysis reveals radiotherapy (p = 0.004) as protective variable and the high S-phase fraction (SPF) (p = 0.001) and stage IIIA (p = 0.012) as risk factors. The SPF appears as an independent prognostic factor for overall survival time. We can build a prognostic index representative of different prognostic groups, which allows us to improve the individual monitoring of these patients.
Apmis | 1992
Juan R. de los Toyos; Primitiva Menendez; Andrés Sampedro; Carlos Hardisson
Gross anatomical and histopathological changes in arthritic joints resulting from oral challenge with Yersinia enterocolitica serotype 0:3, upon pretreatment with desferrioxamine, were always more severe than those induced by intravenous infection of immunized animals. In all the acute inflammation episodes studied, live Yersiniae were isolated from the arthritic region. Invariably, a heavy mixed infiltration of synovia, joint spaces and soft tissues was observed at this stage. Concurrent fibrous thickening and vascular proliferation, along with erosion of articular cartilages and anomalous bone regeneration, were also apparent. In spite of these significant facts, the bacterium could be histopathologically identified only in bone marrow where it developed microcolonies and caused significant necrosis as well. The live bacterium was also retrieved from two‐ and six‐month‐old arthritic ankles/paws examined, but it could not be seen in histological sections of joints. By this time, no cellular infiltration was evident, but there was extensive fibrosis. Bones were at times greatly enlarged, showing a spongeous‐like structure. Additionally, articular cartilages could be completely lost and were substituted by an anomalous ossification filling the joint spaces. This situation led to bone fusion, resembling articular ankylosing traits. In summary, we present the first experimental evidence that Y. enterocolitica serotype 0:3 is a causal agent of osteoarthritis and osteomyelitis, and that it may survive for prolonged periods of time in osseous structures.
Acta Cytologica | 1998
Teresa G. Miralles; Francisco Gosalbez; Primitiva Menendez; Jose-Antonio Manjon; Andrés Sampedro
BACKGROUND Sclerosing lymphocytic lobulitis (SLL) was described in 1948 by Soler and Khardori as fibrotic disease of the breast with histologic features similar to those of Hashimotos thyroiditis. Associations of this process with thyroiditis, artropathy and diabetes mellitus have been seen. CASES We report the fine needle aspiration biopsy (FNAB) findings of two cases of SLL seen in our service. Both patients showed a breast nodule suspicious for malignancy. The cytologic changes vary according to the stage of the disease, from abundant lymphocytes and scanty fibrosis (case 1) to the presence of a few lymphocytes, epithelioid fibroblasts and significant sclerosis (case 2). CONCLUSION The cytologic changes seen in FNAB are sufficient to indicate the diagnosis of SLL. The differential diagnosis has to be made with primary breast lymphoma, periductal or perilobular inflammation and different types of sclerosing breast lesions, depending on the stage of the disease.
Oral Oncology | 2004
David Hardisson; César Álvarez-Marcos; Ana Salas-Bustamante; Marta Alonso-Guervós; Noelia Sastre; Andrés Sampedro
Anticancer Research | 2001
Beatriz Suárez-Álvarez; María del Mar García Suárez; María Eladia Argüelles; Andrés Sampedro; César Álvarez Marcos; Emilia Mira; Frederic A. Van Den Brule; Fu Tong Liu; Partha S. Chowdhury; Juan R. de los Toyos
Microbial Pathogenesis | 1990
J Delostoyos; Jessica L. Vazquez; Andrés Sampedro; Carlos Hardisson
Analytical Cellular Pathology | 2002
Meyke Hermsen; M. Alonso Guervos; G. A. Meijer; J. P. A. Baak; P.J. van Diest; C. Alvarez Marcos; Andrés Sampedro