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1.
Vet J ; 304: 106094, 2024 04.
Artigo em Inglês | MEDLINE | ID: mdl-38452849

RESUMO

This study describes a transversal (TV) ultrasound-guided erector spinae plane (ESP) block technique over the transverse process of T12. And evaluates the distribution of the dye and affected nerves branches compared to a longitudinal (LNG) approach over the transverse process of T12 in canine cadavers. Secondly, it also compares de anatomy and dimensions of the transverse processes of T12 with T9 and T5. For this double-masked, cadaveric experimental study, 12 adult Beagle cadavers were injected with 0.6 mL/kg of dye/contrast. Spread was evaluated by computed tomography (CT) and dissection. Mean bodyweight was 9.76 (±0.59) kg. The TV and LNG approaches stained a median (range) of four (2-6) and three (1-6) medial branches of the dorsal rami of the spinal nerves, three (2-6) and three (2-5) lateral branches, and one (0-3) and one (0-4) ventral branches, respectively. Dye was detected in the epidural space in 55.6% and 66.7% of cases for the TV and LNG approaches, respectively (P=0.63). And in the ventral paravertebral compartment in 22.2% and lymphatics in 88.8% in both approaches. There were no statistical differences for the spread. The dorsolateral edge of the transverse process (TP) was not visible with CT at T12. The mean (±SD) length of the TP was significantly shorter at T12 [3.34 (±0.22)] mm, compared to T9 [6.08 (±0.47)] mm and T5 [5.93 (±0.62)] mm (P <0.001). This study showed similar distribution whether using a TV or LNG approach and differences in the anatomy and length of the T12 TP.


Assuntos
Doenças do Cão , Bloqueio Nervoso , Humanos , Cães , Animais , Bloqueio Nervoso/veterinária , Bloqueio Nervoso/métodos , Vértebras Torácicas , Ultrassonografia/veterinária , Cadáver , Ultrassonografia de Intervenção/veterinária , Ultrassonografia de Intervenção/métodos
2.
J Small Anim Pract ; 62(9): 744-749, 2021 09.
Artigo em Inglês | MEDLINE | ID: mdl-33999425

RESUMO

OBJECTIVES: To review the cause, management and outcome in cats with septic peritonitis within the United Kingdom (2008 to 2018) and to identify if previously identified prognostic factors were associated with survival in this population. MATERIALS AND METHODS: Clinical records from 10 referral hospitals in United Kingdom were reviewed. Data collected included signalment, clinicopathological data and management techniques. Serum albumin, glucose, lactate and ionised calcium concentration; presence of intraoperative hypotension and correct empirical antibiosis were analysed via logistic regression for association with survival. RESULTS: Ninety-five cats were included. The overall survival rate was 66%. Lethargy (89%) and anorexia (75%) were the most common clinical signs, with abdominal pain and vomiting in 44% and 27% of cases, respectively. Gastro-intestinal leakage was the most common source of contamination. The presence of an abdominal mass on clinical examination was not strongly predictive of the presence of neoplasia on histology and did not confer a worse prognosis. Cats presenting with dehiscence of a previous enterotomy/enterectomy did not have a worse prognosis than those presenting with other aetologies. Intraoperative hypotension (adjusted odds ratio 0.173, 95% confidence intervals 0.034 to 0.866, P=0.033) was associated with non-survival. Cats that survived beyond 1 day postoperatively had an improved likelihood of survival (87.5%). All cats that survived beyond 6 days were successfully discharged. CLINICAL SIGNIFICANCE: This study describes the largest group of cats with septic peritonitis with an overall survival rate of 66%. The presence of an abdominal mass on clinical examination or having dehiscence of a previous gastrointestinal surgery did not confer a worse prognosis.


Assuntos
Doenças do Gato , Procedimentos Cirúrgicos do Sistema Digestório , Peritonite , Animais , Doenças do Gato/cirurgia , Gatos , Procedimentos Cirúrgicos do Sistema Digestório/veterinária , Peritonite/cirurgia , Peritonite/veterinária , Prognóstico , Estudos Retrospectivos , Reino Unido/epidemiologia
4.
Clin Exp Immunol ; 182(1): 1-13, 2015 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-26095291

RESUMO

Systemic lupus erythematosus is characterized by the presence of circulating anti-nuclear antibodies (ANA) and systemic damage that includes nephritis, haematological manifestations and pulmonary compromise, among others. Although major progress has been made in elucidating the molecular mechanisms responsible for autoimmunity, current therapies for lupus have not improved considerably. Because the exposure of carbon monoxide (CO) has been shown to display beneficial immunoregulatory properties in different immune-mediated diseases, we investigated whether CO therapy improves lupus-related kidney injury in lupus mice. MRL-Fas(lpr) lupus mice were exposed to CO and disease progression was evaluated. ANA, leucocyte-infiltrating populations in spleen, kidney and lung and kidney lesions, were measured. CO therapy significantly decreased the frequency of activated B220(+) CD4(-) CD8(-) T cells in kidneys and lungs, as well as serum levels of ANA. Furthermore, we observed that CO therapy reduced kidney injury by decreasing proliferative glomerular damage and immune complexes deposition, decreased proinflammatory cytokine production and finally delayed the impairment of kidney function. CO exposure ameliorates kidney and lung leucocyte infiltration and delays kidney disease in MRL-Fas(lpr) lupus mice. Our data support the notion that CO could be explored as a potential new therapy for lupus nephritis.


Assuntos
Monóxido de Carbono/farmacologia , Nefrite Lúpica/terapia , Ativação Linfocitária/efeitos dos fármacos , Animais , Anticorpos Antinucleares/sangue , Complexo Antígeno-Anticorpo/imunologia , Autoanticorpos/biossíntese , Autoanticorpos/imunologia , Monóxido de Carbono/uso terapêutico , Citocinas/biossíntese , Modelos Animais de Doenças , Progressão da Doença , Feminino , Glomérulos Renais/citologia , Glomérulos Renais/imunologia , Glomérulos Renais/lesões , Antígenos Comuns de Leucócito/metabolismo , Pulmão/citologia , Pulmão/imunologia , Camundongos , Camundongos Endogâmicos MRL lpr , Infiltração de Neutrófilos/imunologia , Proteinúria/metabolismo , Baço/citologia , Baço/imunologia , Linfócitos T/imunologia
7.
Rev. chil. pediatr ; 84(2): 160-165, abr. 2013. tab
Artigo em Espanhol | LILACS | ID: lil-687171

RESUMO

Introducción: La Displasia del desarrollo de la cadera (DDC) es un espectro de enfermedades que abarca desde la luxación franca de la cadera hasta la displasia acetabular leve. El screening de detección de DDC se realiza de rutina en nuestro país, mediante una radiografía de pelvis a los 3 meses. El índice acetabular medido en estas radiografías se utiliza para evaluar la cadera displásica, tanto en la presentación inicial como durante el seguimiento posterior. Objetivo: Evaluar la variabilidad tanto intra como inter observador en la medición del índice acetabular, entre profesionales médicos. Material y Métodos: Cuatro evaluadores (un cirujano-ortopédico infantil, un médico general, un pediatra y un radiólogo) realizaron la medición del índice acetabular en 100 radiografías de screening (200 caderas), en tres ocasiones, separadas por un mes cada una (600 mediciones totales). Un observador independiente evaluó la reproductibilidad en la medición. Se utilizó el coeficiente de correlación intraclase para determinar diferencias significativas. Resultados: La variabilidad intra observador fue menor que la interobservador. La variabilidad intra observador fue similar para los diferentes evaluadores, +/- 1,5°. La variabilidad inter observador fue de +/- 3,4°. Conclusiones: Demostramos una alta concordancia entre las mediciones, determinando una alta reproductibilidad del índice acetabular. El índice acetabular es un método seguro para el diagnóstico y seguimiento de displasia acetabular.


Developmental dysplasia of the hip (DDH) is a spectrum of diseases ranging from frank dislocation of the hip to mild acetabular dysplasia. DDH screening for detection is performed routinely in our country using pelvic x-ray at 3 months of age. The radiographic measured acetabular index is used to evaluate the dysplastic hip, at initial presentation and during follow-up. Objective: Evaluation of the intra- and inter-observer variability, among medical professionals, when measuring acetabular index. Methods: Four reviewers (a children orthopedic surgeon, a general practitioner, a pediatrician and a radiologist) performed acetabular index measurement in 100 radiographs (200 hips), on three occasions, separated each by one month (600 total measurements). An independent observer evaluated the measurement reproducibility. The intra-class correlation coefficient to determine significant differences was used. Results: The intra-observer variability was less than the inter-observer variability. The intra-observer variability was similar among the different assessors, +/- 1.5 degrees. The inter-observer variability was +/- 3.4 degrees. Conclusions: A high concordance among measurements was reported, evidencing a high reproducibility of the acetabular index; this index is a reliable method for the diagnosis and follow-up of acetabular dysplasia.


Assuntos
Humanos , Lactente , Acetábulo/patologia , Acetábulo , Luxação Congênita de Quadril/patologia , Luxação Congênita de Quadril , Variações Dependentes do Observador , Reprodutibilidade dos Testes , Programas de Rastreamento/métodos
8.
Rev. chil. radiol ; 18(3): 121-128, 2012. ilus, tab
Artigo em Espanhol | LILACS | ID: lil-658853

RESUMO

Radiosynovectomy is a local form of radiotherapy used as second-line treatment in the management of inflammatory and non-inflammatory arthropathies with unsatisfactory response to local or systemic corticosteroid therapy. Its efficacy is similar to that of surgical synovectomy, with the advantages of being a low-cost and minimally- invasive treatment that requires a shorter recovery time. Its efficacy is greater in the treatment of inflammatory arthritis characterized by synovitis, such as rheumatoid arthritis and juvenile chronic arthritis with mono/oligoarticular involvement, especially in upper extremity joints. A number of isotopes can be used in colloidal suspensions. Rhenium-186-sulphide colloid is currently indicated for the treatment of medium-sized joints. The ultrasound-guided injection is suitable for small joints, such as wrist. For proper and safe use and administration of this technique the collaboration of a trained and experienced radiologist is critical to successful treatment.


La radiosinovectomía es una forma local de radioterapia utilizada como tratamiento de segunda línea en el manejo de artropatías inflamatorias y no inflamatorias con respuesta insatisfactoria a la terapia sistémica o local con corticoesteroides. Tiene una eficacia similar a la sinovectomía quirúrgica, con las ventajas de ser un tratamiento de menor costo, menos cruento y con menor tiempo de convalecencia. Su eficacia es mayor en artropatías inflamatorias caracterizadas por sinovitis, como la artritis reumatoide y artritis crónica juvenil, con compromiso mono u oligoarticular y en articulaciones de extremidades superiores. Existen múltiples isótopos que se pueden utilizar en suspensiones coloidales, siendo el sulfuro coloidal de renio-186 el utilizado para la articulación radiocarpiana. Una técnica de administración adecuada es fundamental para el éxito del tratamiento, siendo la inyección con guía ultrasonográfica adecuada para articulaciones de volumen pequeño, instancia en la que la colaboración del médico radiólogo entrenado es fundamental.


Assuntos
Feminino , Artrite Juvenil/terapia , Rênio/uso terapêutico , Sinovite/terapia , Ultrassom/métodos , Artrite Juvenil/complicações , Injeções Intra-Articulares , Punho , Compostos Radiofarmacêuticos/uso terapêutico , Seleção de Pacientes , Sinovite/etiologia , Terapia Combinada
9.
Neuroscience ; 189: 236-49, 2011 Aug 25.
Artigo em Inglês | MEDLINE | ID: mdl-21619912

RESUMO

Whereas some studies suggest that alpha rhythm promotes information processing in the human cortex (processing hypothesis), other studies suggest its involvement in an active cortical idling which prevents the interfering action of irrelevant information (idling hypothesis). In this study, this apparent contradiction was analyzed using a computing procedure which distinguishes phase-locked and non-phase-locked alpha response during the execution of a complex event-related visual-motor task. The electroencephalographies (EEGs) of 12 male volunteers were digitized (128 electrodes), band-pass filtered for isolating α wave, and event-related averaged during the execution of the visual-motor tasks. This procedure showed a phase-locked α response to stimuli and suppressed the non-phase-locked response. When EEG envelope of the α-wave was computed (Hilbert transformation) before the event-related average, the response of the alpha amplitude to stimuli was observed while the phase-locked α response vanished. Visual stimuli induced a short-lasting increase of phase-locked alpha activity and a long-lasting decrease of non-phase-locked alpha activity whose latency and amplitude changed with the cortical region (visual vs. parietal vs. frontal cortex), with the sensory-semantic information of visual stimuli, and with the tasks associated to them (comparing the alpha response to stimuli which were used for a visual-motor tasks with those passively observed). Alpha sub-bands around the individual alpha frequency peak showed a different phase-locked response. Finally, two early evoked potentials (C1-P1) showed a time latency similar to that computed for the phase-locked alpha response, suggesting that early evoked potentials are modified by the superposition of this alpha activity. Present data suggest that alpha activity promotes the cortical processing of information by increasing the phase-locked alpha activity and by decreasing the non-phase-locked alpha activity, and disturbs cortical processing under basal conditions when it is not phase-locked to any particular task.


Assuntos
Ritmo alfa , Desempenho Psicomotor , Percepção Visual , Adulto , Potenciais Evocados , Humanos , Masculino , Pessoa de Meia-Idade , Córtex Motor/fisiologia , Lobo Parietal/fisiologia , Estimulação Luminosa , Córtex Visual/fisiologia , Adulto Jovem
11.
Rev. chil. radiol ; 14(2): 62-67, 2008. ilus, tab
Artigo em Espanhol | LILACS | ID: lil-517430

RESUMO

Background. Giant cell tumor (GCT) is an uncommon primary bone neoplasm in pediatric patients. Plain radiograph of the affected area is the first diagnostic approach in most cases. Objective. To show radiographic features that could allow the radiologist to suspect the diagnosis of GCT through plain radiological study. Methods. Records from the National Bone Tumor File between 1959 and 1999 were retrospectively analyzed. Twenty-nine cases of patients under 20 years with biopsy proven diagnosis of GCT were found. The radiological study was available in 14 cases. Results. From a total of 29 patients, 83 percent were females and 17 percent males. Age ranged from 7 to 19 years, with an average of 16.3 years. In cases with radiological study, 93 percent of them presented epiphyseal involvement of long bones. Osteolytic lesions with metaphyseal extension were the most frequent radiological pattern. One case showed malignancy with metastases. Conclusions. GCT is regarded as an infrequent occurrence in pediatric patients and its diagnosis can be suspected based on plain radiographic findings.


El tumor de células gigantes es un tumor óseo primario, poco frecuente en población pediátrica. En la mayoría de los casos, la radiografía simple es la primera aproximación diagnóstica, por lo que nuestro objetivo es mostrar las características radiológicas que permiten sospechar el diagnóstico del tumor de células gigantes en el estudio radiológico simple. Se analizó retrospectivamente los datos del Registro Nacional de Tumores Óseos, entre los años 1959 y 1999, encontrando 29 casos de tumor de células gigantes histológicamente confirmados en menores de 20 años; en 14 se dispuso de estudio radiológico. El 83 por ciento (24/29) correspondió a mujeres y 17 por ciento (5/29) a hombres, con edades entre 7 y 19 años (promedio = 16.3 años). Radiológicamente, el 93 por ciento mostró compromiso epifisiario de huesos largos y el patrón más frecuente fue osteolítico con extensión metafisiaria.


Assuntos
Humanos , Masculino , Adolescente , Feminino , Criança , Neoplasias Ósseas , Tumor de Células Gigantes do Osso , Neoplasias Ósseas/patologia , Estudos Retrospectivos , Tumor de Células Gigantes do Osso/patologia
13.
An Otorrinolaringol Ibero Am ; 33(5): 521-7, 2006.
Artigo em Espanhol | MEDLINE | ID: mdl-17091866

RESUMO

Primary ciliary dyskinesia is a disorder characterized by the presence of recurrent infections of the superior and inferior respiratory tract. It is caused by a recessive autosomic genetic disorder. Its diagnosis is often given late, because other diagnostic possibilities are thought of first. It is common to find many previous visits to the ENT specialist in a medical record. The final diagnosis is given by electronic microscopy observing the ciliary defect, which is frequently due to the absence or anomalies of dineine in the arms and in the structures of the microtubule pairs responsible of movement. The mucus to study is usually obtained from the inferior nasal concha. In the rest of cases the mucus of the tracheobronchial apparatus is only studied if a fibrobronchoscopy is necesary in order to evaluate bronchial compromise or when the nasal sample is not sufficient. The ENT specialist must be alert in order to be able to think of this entity. The genetic advice is the best way to prevent it.


Assuntos
Transtornos da Motilidade Ciliar/diagnóstico , Transtornos da Motilidade Ciliar/genética , Transtornos da Motilidade Ciliar/terapia , Humanos
14.
An. otorrinolaringol. Ibero-Am ; 33(5): 521-527, sept.-oct. 2006.
Artigo em Es | IBECS | ID: ibc-049064

RESUMO

La DCP es un trastorno caracterizado por la presencia de infecciones recurrentes del tracto respiratorio superior e inferior. Obedece a un trastorno genético autosómico recesivo. Su diagnóstico en no pocas oportunidades se realiza tardíamente porque se piensa en otras posibilidades diagnósticas: Es habitual que en la historia clínica se recoja el antecedente de múltiples visitas al ORL. El diagnóstico definitivo se realiza por microscopía electrónica observando el defecto ciliar, que obedece frecuentemente a la ausencia o anomalías en los brazos de dineína y en las estructuras de los pares de microtúbulos responsables del movimiento. La mucosa para estudio se obtiene del comete inferior de manera habitual. Por lo demás la mucosa del aparato traqueobronquial se estudia solo si se precisara de fibrobroncoscopia para evaluar el compromiso bronquial o cuando no sea rentable la muestra nasal. El otorrinolaringólogo debe de estar alerta para ser capaz de pensar en esta entidad. El consejo genético es la mejor medida para prevenirla


Primary ciliary dyskinesia is a disorder characterized by the presence of recurrent infections ofthe superior and inferior respiratory tract. It is caused by a recessive autosomic genetic disorder. Its diagnosis is often given late, because other diagnostic possibilities are thought of first. It is common to find many previous visits to the ENT specialist in a medical record. The final diagnosis is given by electronic microscopy observing the ciliary defect, which is frequently due to the absence or anomalies of dineine in the arms and in the structures ofthe microtubule pairs responsible of movement. The mucus to study is usually obtained from the inferior nasal concha. In the Test of cases the mucus of the tracheobronchial apparatus is only studied if a fibrobronchoscopy is necesary in order to evaluate bronchial compromise or when the nasal sample is not sufficient. The ENT specialist must be alert in order to be able to think ofthis entity. The genetic advice is the best way to prevent it


Assuntos
Humanos , Transtornos da Motilidade Ciliar/diagnóstico , Transtornos da Motilidade Ciliar/genética , Transtornos da Motilidade Ciliar/terapia
15.
Scand J Rheumatol ; 35(2): 143-6, 2006.
Artigo em Inglês | MEDLINE | ID: mdl-16641050

RESUMO

We report the case of a 50-year-old man who presented with systemic vasculitis associated with Fasciola hepatica infection. The patient presented with severe skin, kidney, spleen, ophthalmic, and neurological compromise. An immunological examination for primary vasculitis was negative and other infections were discounted by microbiological and serological analyses. The patient was treated with steroids without clinical response. The Fasciola hepatica infection was confirmed by the presence of specific immunoglobulin G (IgG) serum antibodies detected by a quantitative enzyme-linked immunosorbent assay (ELISA) with an optical density (OD) of 0.483 OD units (normal value<0.170 OD units) and a high-titre complement fixation (1/80 dilution). The patient received treatment with triclabendazole and all symptoms and systemic manifestations resolved within weeks. Hence, this previously unreported vasculitis-associated infection, if identified opportunely, can be treated and cured.


Assuntos
Fasciola hepatica/isolamento & purificação , Fasciolíase/complicações , Vasculite/etiologia , Animais , Anti-Helmínticos/uso terapêutico , Anticorpos Anti-Helmínticos/análise , Benzimidazóis/uso terapêutico , Diagnóstico Diferencial , Ensaio de Imunoadsorção Enzimática , Fasciola hepatica/imunologia , Fasciolíase/tratamento farmacológico , Fasciolíase/parasitologia , Seguimentos , Humanos , Masculino , Pessoa de Meia-Idade , Triclabendazol , Vasculite/diagnóstico , Vasculite/tratamento farmacológico
16.
Scand J Rheumatol ; 35(6): 435-40, 2006.
Artigo em Inglês | MEDLINE | ID: mdl-17343250

RESUMO

OBJECTIVE: To investigate the influence of -308 tumour necrosis factor-alpha (TNFalpha) promoter polymorphism and circulating TNFalpha levels in the clinical response to adalimumab treatment in patients with rheumatoid arthritis (RA). METHODS: Eighty-one patients with active RA were genotyped for the -308 TNFalpha polymorphism by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analysis and subdivided into two groups for each polymorphism (G/A and G/G genotype). All received 40 mg of adalimumab subcutaneously every other week. We compared the groups' clinical responses to adalimumab at 8, 16, and 24 weeks using the Disease Activity Score in 28 joints (DAS28). RESULTS: Both groups showed a significant improvement from baseline. A significant difference between groups was found at week 24. We found that 88.2% of G/G versus 68.4% of G/A for the -308 polymorphism were DAS28 responders (p = 0.05). The score improvement at week 24 was 2.5 +/- 1.3 in the G/G group and 1.8 +/- 1.3 in the G/A group for the -308 polymorphism (p = 0.04). The median of serum TNFalpha levels of the G/A group were lower than those of the G/G group, and statistically different at weeks 8 and 24 (p < 0.039 and p < 0.043). When comparing baseline levels to those achieved at 8, 16, and 24 weeks for the whole group, only responder patients showed a statistically significant overall increase in TNFalpha over time (p < 0.000001). CONCLUSION: A relationship between DAS28 improvement, the -308 G/G polymorphism, and increased circulating TNFalpha levels was found in Chilean RA patients treated with adalimumab.


Assuntos
Anticorpos Monoclonais/uso terapêutico , Antirreumáticos/uso terapêutico , Artrite Reumatoide/tratamento farmacológico , Fator de Necrose Tumoral alfa/genética , Adalimumab , Adulto , Anticorpos Monoclonais/efeitos adversos , Anticorpos Monoclonais Humanizados , Antirreumáticos/efeitos adversos , Artrite Reumatoide/sangue , Chile , Genótipo , Humanos , Pessoa de Meia-Idade , Polimorfismo de Nucleotídeo Único , Regiões Promotoras Genéticas , Fatores de Tempo , Resultado do Tratamento , Fator de Necrose Tumoral alfa/antagonistas & inibidores , Fator de Necrose Tumoral alfa/sangue
18.
Rev. chil. radiol ; 11(1): 9-12, 2005. ilus
Artigo em Espanhol | LILACS | ID: lil-449896

RESUMO

El fenómeno de invaginación en el adulto es un evento poco frecuente, con una amplia variedad de presentación, que va desde síntomas agudos de obstrucción intestinal, hasta síntomas abdominales crónicos inespecíficos. Puede ocurrir tanto en intestino delgado como colon, siendo frecuente encontrar lesiones orgánicas subyacentes, en su mayoría procesos neoplásicos, tanto benignos como malignos. Estos últimos son la etiología principal de invaginaciones en intestino grueso. El diagnóstico se puede realizar de forma confiable con el uso de tomografía computada al identificarse características imagenológicas particulares a esta patología. Reportamos dos casos en pacientes que se presentan con síntomas de obstrucción intestinal, con lesiones subyacentes en ambos casos, un lipoma y una neoplasia maligna.


Assuntos
Masculino , Humanos , Feminino , Pessoa de Meia-Idade , Intussuscepção , Lipoma/complicações , Neoplasias do Colo/complicações , Colonoscopia , Colo , Intussuscepção/etiologia , Lipoma/diagnóstico , Obstrução Intestinal/etiologia , Radiografia Abdominal
19.
Rev. chil. radiol ; 11(4): 166-169, 2005. ilus
Artigo em Espanhol | LILACS | ID: lil-436620

RESUMO

Traumatic injuries of the diaphragm are a known consequence of severe trauma, usually of the blunt type. Its incidence is increasing due to the rise in number and severity of accidents, especially car accidents. Diagnosing a traumatic diaphragmatic rupture is still a challenge for both radiologists and surgeons, with a delayed diagnosis in more than half of cases, with the consequent development of latent hernia. This hernia may manifest with symptoms varying from unspecific to bowel strangulation. We present the case of a patient with colonic obstruction secondary to a traumatic diaphragmatic hernia, with previous history of a penetrating thoracoabdominal trauma seven years before. Radiologic methods and signs for the diagnosis of this pathology are reviewed.


Resumen: Las lesiones traumáticas del diafragma son consecuencia conocida de un trauma grave, gene-ralmente de tipo contuso. Su incidencia ha aumentado debido al crecimiento en número y severidad de los accidentes, en especial del tránsito. Su diagnóstico continúa siendo un desafío para cirujanos y radiólogos, diagnosticándose tardíamente hasta en más de la mitad de los casos, dejando una hernia diafragmática latente, que puede manifestarse con síntomas que varían desde inespecíficos hasta la estrangulación de un asa intestinal. Se presenta el caso de un paciente con obstrucción intestinal de colon secundaria a una hernia diafragmática traumática atascada, con historia de un traumatismo penetrante toracoabdominal ocurrido siete años antes. Se revisan los métodos y signos radiológicos de mayor utilidad para el diagnóstico de esta patología.


Assuntos
Masculino , Humanos , Idoso , Hérnia Diafragmática Traumática/complicações , Hérnia Diafragmática Traumática , Doenças do Íleo , Obstrução Intestinal/etiologia , Obstrução Intestinal , Ferimentos Penetrantes/complicações , Resultado do Tratamento
20.
Genet. mol. res. (Online) ; 4(3): 543-552, 2005. ilus, graf, tab
Artigo em Inglês | LILACS | ID: lil-444957

RESUMO

Reconfigurable systolic arrays can be adapted to efficiently resolve a wide spectrum of computational problems; parallelism is naturally explored in systolic arrays and reconfigurability allows for redefinition of the interconnections and operations even during run time (dynamically). We present a reconfigurable systolic architecture that can be applied for the efficient treatment of several dynamic programming methods for resolving well-known problems, such as global and local sequence alignment, approximate string matching and longest common subsequence. The dynamicity of the reconfigurability was found to be useful for practical applications in the construction of sequence alignments. A VHDL (VHSIC hardware description language) version of this new architecture was implemented on an APEX FPGA (Field programmable gate array). It would be several magnitudes faster than the software algorithm alternatives.


Assuntos
Humanos , Algoritmos , Alinhamento de Sequência/métodos , Biologia Computacional/métodos , Software , Fatores de Tempo , Modelos Genéticos , Simulação por Computador
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