Browsing by Author "Ribeiro, F"
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- Acute Kidney Injury in the Context of Inflammatory Bowel Disease - A Clinical CasePublication . Cristóvão Marques, J; Barata, R; Lemos Garcia, J; Navarro, D; Góis, M; Sousa, H; Cotovio, P; Ribeiro, F; Nolasco, FExtraintestinal manifestations of inflammatory bowel disease are common and extendable to all organs. Kidney and lower genitourinary system occurs in 4-23% of cases. This may be dependent on inflammatory bowel disease activity, secondary to metabolic disorders, drugs or others. We present a case of a 68-year-old man with ulcerative colitis for 22 years admitted in our department for acute nephritic syndrome. Urinary microscopy suggested glomerular injury. A kidney biopsy was performed and was compatible with acute interstitial nephritis and IgA nephropathy. Toxicity of mesalazine and glomerulonephritis secondary to ulcerative colitis were assumed. The patient suspended mesalazine and started prednisolone with clinical improvement. Our purpose is to sensitize the importance of having a prompt and thorough evaluation of acute kidney injury in patients with inflammatory bowel disease. We briefly review the broad spectrum of kidney manifestations in this population, focusing on mesalazine-induced nephrotoxicity.
- Acute-on-Chronic Liver Failure: A Portuguese Single-Center Reference ReviewPublication . Verdelho, M; Perdigoto, R; Machado, J; Mateus, É; Marcelino, P; Pereira, R; Fortuna, P; Bagulho, L; Bento, L; Ribeiro, F; Nolasco, F; Martins, A; Barroso, EAcute-on-chronic liver failure (ACLF) is a syndrome characterized by an acute deterioration of a patient with cirrhosis, frequently associated with multi-organ failure and a high short-term mortality rate. We present a retrospective study that aims to characterize the presentation, evolution, and outcome of patients diagnosed with ACLF at our center over the last 3 years, with a comparative analysis between the group of patients that had ACLF precipitated by infectious insults of bacterial origin and the group of those with ACLF triggered by a nonbacterial infectious insult; the incidence of acute kidney injury and its impact on the prognosis of ACLF was also analyzed. Twenty-nine patients were enrolled, the majority of them being male (89.6%), and the mean age was 53 years. Fourteen patients (48.3%) developed ACLF due to a bacterial infectious event, and 9 of them died (64.2%, overall mortality rate 31%); however, no statistical significance was found (p < 0.7). Of the remaining 15 patients (51.7%) with noninfectious triggers, 11 died (73.3%, overall mortality rate 37.9%); again there was no statistical significance (p < 0.7). Twenty-four patients (83%) developed acute kidney injury (overall mortality rate 65.5%; p < 0.022) at the 28-day and 90-day follow-up. Twelve patients had acute kidney injury requiring renal replacement therapy (41.37%; overall mortality rate 37.9%; p < 0.043). Hepatic transplant was performed in 3 patients, with a 100% survival at the 28-day and 90-day follow-up (p < 0.023). Higher grades of ACLF were associated with increased mortality (p < 0.02; overall mortality 69%). CONCLUSIONS: ACLF is a heterogeneous syndrome with a variety of precipitant factors and different grades of extrahepatic involvement. Most cases will have some degree of renal dysfunction, with an increased risk of mortality. Hepatic transplant is an efficient form of therapy for this syndrome.
- An Atypical Presentation of Thrombotic Microangiopathy After Lung Transplant: a Case ReportPublication . Menezes, MM; Aires, I; Semedo, L; Calado, J; Ribeiro, F; Nolasco, FThrombotic microangiopathy (TMA) is a pathologic condition characterized by microangiopathic hemolytic anemia, thrombocytopenia, and organ injury due to microvascular endothelial lesions and thrombosis. It occurs in a variety of diseases and, unless recognized and treated, leads to severe morbidity and mortality. We present the case of a 48-year-old woman who underwent lung transplantation, initially under tacrolimus, mycophenolate mofetil (MMF), and prednisolone. Several complications emerged in the following months, including abdominal aortic and left renal artery thrombosis and cutaneous infections, although her renal function remained normal. Six months after transplant, her renal function began to deteriorate, which was assumed to be due to elevated tacrolimus levels and doses were adjusted. Due to leukopenia, MMF was changed to everolimus. One year after, she was admitted with fatigue, anemia, and renal dysfunction. Complementary exams revealed only iron deficiency, leukopenia, normal platelets, and elevated lactate dehydrogenase; her renal ultrasound was normal. A renal biopsy was performed and thrombotic microangiopathy was subsequently identified as the main cause of the renal dysfunction. Tacrolimus was therefore discontinued and MMF restarted with slow improvement of renal function. Only when everolimus was stopped did the patient's renal function show incremental improvement. TMA may be a serious complication after lung transplantation and the risk is higher when a combination of tacrolimus and everolimus is used. Renal biopsy findings are essential to confirm the final diagnosis of TMA, allowing for a change in immunosuppression to prevent permanent and severe renal damage.
- Complicações Hipertensivas na Gravidez. 1 Mês na Maternidade Dr. Alfredo da CostaPublication . Lermann, R; Ribeiro, F; Dias, E; Campos, AA patologia hipertensiva ocorre em 6 a 8% das gravidezes e é a segunda causa de morte materna, contribuindo com 15% para essa taxa de mortalidade. É também causa significativa de morte fetal e morbi-mortalidade neonatal. O objectivo deste trabalho foi avaliar, através de uma análise retrospectiva, as complicações hipertensivas na população de grávidas que tiveram o parto na Maternidade Dr. Alfredo da Costa (MAC) em Novembro de 2005. Durante este período 41 mulheres (10,1%) tiveram complicações hipertensivas. Treze grávidas (31,7%) tinham hipertensão crónica, dezanove (46,3%) HIG, 5 (12,2%) PE moderada e 7 (17%) PE grave, com 3 casos de síndrome HELLP. Registou-se um caso de síndrome HELLP sem hipertensão arterial. Registaram-se 9 casos de parto prematuro (22,5%) e uma morte fetal. A idade gestacional média foi 37 semanas. Assinalaram-se 9,7% de RCIU e nenhum caso de asfixia neonatal.
- Hipertiroidismo na Gravidez – um Caso ClinicoPublication . Ribeiro, F; Cordeiro, A; Rocha, T; Borges, A; Campos, ACThyroid disease is common in pregnant women.We report a 10 weeks gestation pregnancy with hyperemesis gravidarum, hypertension crisis and hyperthyroidism
- Ingestão dos Alimentos Cozinhados na Alergia Alimentar ao Leite de Vaca e ao OvoPublication . Rosa, S; Ribeiro, F; Leiria-Pinto, PO leite de vaca e o ovo são responsáveis pela maioria dos casos de alergia alimentar na infância. O processamento térmico dos alimentos pode alterar a sua alergenicidade e estão publicados vários estudos que investigaram a tolerância ao leite de vaca e ao ovo cozinhados em doentes com alergia ou com sensibilização aos mesmos. Da avaliação destes estudos verificou‑se que os alimentos cozinhados são tolerados pela maioria da população incluída nos mesmos e que a sua ingestão é segura, podendo melhorar a qualidade de vida dos doentes. No entanto, a influência desta ingestão na história natural da alergia alimentar e na aquisição de tolerância ao alimento cru é discutível e necessita de mais estudos. Não foram encontrados marcadores clínicos ou imunológicos fiáveis que permitam a identificação dos doentes que toleram os alimentos cozinhados, pelo que a prova de provocação oral se mantém o único método fiável para avaliar essa tolerância.
- Molecular Profile of Sensitization to Dermatophagoides Pteronyssinus Dust Mite in PortugalPublication . Limão, R; Spínola Santos, A; Araújo, L; Cosme, J; Inácio, F; Tomaz, E; Ferrão, A; Santos, N; Sokolova, A; Môrete, A; Falcão, H; Cunha, L; Ferreira, A; Bras, A; Ribeiro, F; Lozoya, C; Leiria-Pinto, P; Prates, S; Plácido, J; Coimbra, A; Taborda-Barata, L; Pereira Santos, MC; Pereira Barbosa, M; Pineda, FBackground and objectives: To analyze component-resolved diagnosis of sensitization to Dermatophagoides pteronyssinus (Der p) in patients with respiratory allergy and the association between diagnostic findings and clinical severity in different geographical areas. Methods: The study population comprised 217 patients (mean age, 25.85 [12.7] years; 51.16% female) selected from 13 centers in Portugal (5 from the North, n=65). All had allergic rhinitis with or without asthma and positive skin prick test results to at least 1 dust mite. Specific IgE (sIgE) to Der p, Dermatophagoides farinae, Lepidoglyphus destructor, Der p 1, Der p 2, Der p 10, and Der p 23 was determined using ImmunoCAP. The Mann-Whitney test was applied for the following comparisons: rhinitis vs rhinitis and asthma; mild vs moderate-to-severe rhinitis; North vs South. Results: The prevalence of sensitization was 98.2% for Der p, and 72.4%, 89.4%, 9.7%, and 77% for Der p 1, Der p 2, Der p 10, and Der p 23, respectively. The corresponding median sIgE levels were 8.56, 17.7, 0.01, and 3.95 kUA/L. sIgE to all allergens was higher in patients with moderate-to-severe rhinitis and rhinitis with asthma (nonsignficant). Concentrations of sIgE to Der p 2 were significantly higher in the South than in the North (P=.0496). Conclusion: The most common sensitization in Portugal was to Der p. The highest prevalence and median sIgE level were observed for Der p 2. All sIgE values for molecular components were higher in more symptomatic patients (nonsignificant). Concentrations of sIgE to Der p 2 were higher in the South, probably because of the warmer temperature and/or the larger sample size.
- Nephrotic Syndrome in HIV/HCV Co-Infected PatientPublication . Viana, H; Mesquita, I; Azevedo, A; Ribeiro, F; Carvalho, F; Nolasco, F
- Oxalate Nephropathy Following Roux‑en‑Y Gastric Bypass Surgery – Mini‑ReviewPublication . Verdelho, M; Mendes, M; Ribeiro, F; Sousa Viana, H; Carvalho, F; Nolasco, FOxalate Nephropathy is characterised by the presence of tubular crystalline deposits of calcium oxalate, which can lead to both acute and chronic tubular injury and progressive renal failure. Enteric hyperoxaluria is the most common cause of moderate hyperoxaluria; it occurs in conditions associated with fat or bile acid malabsorption, which include jejunoileal bypass and other bariatric procedures such as Roux‑en‑Y gastric bypass surgery. We present the clinical case of a 69‑year‑old man who was hospitalised for non‑oliguric renal dysfunction, with a serum creatinine of 10 mg/dl and normocytic normochromic anaemia. There was no prior history of renal disease. Twenty months before admission the patient was diagnosed with a gastro‑oesophageal junction adenocarcinoma and was treated with pre‑operative chemotherapy, followed by total gastrectomy, with a Roux‑en‑Y gastric bypass reconstruction. On discharge from gastric surgery, renal function was normal. On the first day of hospital stay haemodialysis was initiated. Over the following days, the rapid unexplained renal impairment was investigated, and this workup [2] included a kidney biopsy. Histological examination of the biopsy specimen revealed a predominantly interstitial nephropathy with tubular atrophy and interstitial fibrosis, with bright intra‑tubular calcium oxalate crystals in over 50% of the tubules and so the histological diagnosis was of oxalate nephropathy. Subsequently, no recovery of renal function was observed, so the patient is currently undergoing regular haemodialysis. Oxalate nephropathy is a rare but severe complication of Roux‑en‑Y gastric bypass surgery that can lead to a rapid progression to kidney failure. Although the treatment of obesity is the main indication for this surgery, this is also the preferred approach for gastrointestinal reconstruction after total gastrectomy for treatment of gastric carcinoma. Considering the rapid progression of oxalate nephropathy to kidney failure, patients who undergo Roux‑en‑Y gastric bypass surgery should have regular follow‑up of renal function.
- Pré-Eclâmpsia Grave. Compromisso Materno e FetalPublication . Júlio, C; Ribeiro, F; Lermann, R; Reis, J; Bettencourt, B; Matos, C; Tomé, T; Dias, E; Campos, AIntrodução: A pré-eclâmpsia (PE) é uma síndrome específica da gravidez, associado a morbimortalidade materna e perinatal. Métodos: Estudo retrospectivo descritivo das 134 gestações com PE grave, seguidas na nossa instituição de 2003 a 2005, com o objectivo de avaliar as repercussões maternas e fetais desta patologia. Resultados: Na maioria dos casos houve repercussão sistémica, manifestada por sintomatogia (79%) e valores laboratoriais indicativos de gravidade clínica. Os dados ecográficos revelaram 22,7% de restrição de crescimento intra-uterino e 21,3% de fluxometria doppler patológica. Decidiu-se interromper electivamente a gravidez em 95,3% dos casos, 60,5% nas primeiras 48h, sendo a síndrome materno a principal indicação. Verificaram-se 4 abortos e 5 mortes fetais. O parto ocorreu antes das 34 semanas em 63,1% dos casos. Em 82,8% a via de parto foi cesariana. Salientam-se 4 casos de insuficiência renal aguda e 2 casos de acidente vascular cerebral hemorrágico com morte materna. 20% dos recém-nascidos eram leves para a idade gestacional e verificou-se asfixia neonatal em 7,7%. Conclusão: A pré-eclâmpsia grave continua a ser uma patologia com implicações importantes no desfecho obstétrico.