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1.
Colorectal Dis ; 20(7): 597-605, 2018 07.
Artículo en Inglés | MEDLINE | ID: mdl-29383826

RESUMEN

AIM: Increasing scrutiny on both individual and unit outcomes after surgical procedures is now expected. In the field of inflammatory bowel disease, this is particularly pertinent for outcomes after ileoanal pouch surgery. METHOD: The Surgical Workload and Outcomes Research Database (SWORD) relies on administrative data derived from Hospital Episode Statistics collected in England. The platform was interrogated for pouch procedures undertaken in England between April 2009 and December 2016 to assess national caseload and, between April 2012 and December 2016, to assess variation in caseload and outcomes after pouch surgery. RESULTS: In England there is a suggestion that numbers of pouch procedures may be decreasing. Over 80% of Trusts offering pouch surgery do so at very low volume with less than five procedures per year. There is also a clear phenomenon of the occasional pouch surgeon with 126 surgeons undertaking just one pouch operation during the study period of almost 5 years. Laparoscopic practice varies but 60% of pouches overall were done via an open approach. Mean length of stay was 10.1 days and average 30-day readmission rates were 27.4%. Outside London there appears to be an increasing trend for higher volume units to do more adult pouch procedures and lower volume units to do fewer. CONCLUSION: Low volume units and occasional pouch surgeons present a strong argument for centralization of pouch surgery. Data from England outside London suggest that this may already be happening.


Asunto(s)
Reservorios Cólicos/estadística & datos numéricos , Cirugía Colorrectal/organización & administración , Enfermedades Inflamatorias del Intestino/cirugía , Evaluación de Resultado en la Atención de Salud/estadística & datos numéricos , Carga de Trabajo/estadística & datos numéricos , Adulto , Servicios Centralizados de Hospital/organización & administración , Inglaterra , Femenino , Humanos , Masculino
2.
Colorectal Dis ; 20(10): 913-922, 2018 10.
Artículo en Inglés | MEDLINE | ID: mdl-29927537

RESUMEN

AIM: The second Association of Coloproctology of Great Britain and Ireland (ACPGBI) Ileoanal Pouch Registry (IPR) report was released in July 2017 following a first report in 2012. This article provides a summary of data derived from the most recent IPR report (2017 Ileoanal Pouch Report. https://www.acpgbi.org.uk/content/uploads/2016/07/Ileoanal-Pouch-Report-2017-FINAL.compressed.pdf). METHOD: The IPR is an electronic database of voluntarily submitted data including patient demographics, disease, intra-operative and postoperative factors submitted by consultant surgeons or delegates. Data up to 31 March 2017 have been analysed for this report. RESULTS: A total of 5352 pouch operations were carried out at 76 UK and four European centres by 154 surgeons over four decades. Recorded procedures have increased over time but data submission is voluntary and underestimates actual volume. Significant variation exists in institutional volume; 73 centres entered data on patients undergoing pouch surgery during the past 5 years. Of these, 44 centres have submitted ≤ 10 cases, with 10 centres submitting one patient and nine centres two cases. Since 2013, minimal access surgery has been employed in 54% of cases. Rectal dissection was undertaken in the total mesorectal excision plane in 69%. J-pouch configuration was used in 99% of cases and 90% of pouch-anal anastomoses were performed using a stapled technique. Including all years, the IPR rate of pelvic sepsis was 9.4% and the rate of pouch failure was 4.7%. CONCLUSION: The IPR holds the largest voluntary repository of data on ileoanal pouch surgery. The second report from the IPR records marked refinements in surgical technique over time but also highlights wide variation in institutional caseload and outcome across the UK.


Asunto(s)
Reservorios Cólicos/estadística & datos numéricos , Cirugía Colorrectal/estadística & datos numéricos , Pautas de la Práctica en Medicina/estadística & datos numéricos , Adulto , Femenino , Humanos , Masculino , Persona de Mediana Edad , Sistema de Registros , Reino Unido , Adulto Joven
3.
Colorectal Dis ; 20(8): O181-O189, 2018 08.
Artículo en Inglés | MEDLINE | ID: mdl-29768701

RESUMEN

AIM: It is well established that ileo-anal pouch-related septic complications (PRSC) increase the risk of pouch failure. There are a number of publications that describe the management of early PRSC in ulcerative colitis (UC) in small series. This article aims to systematically review and summarize the relevant current data on this subject and provide an algorithm for the management of early PRSC. METHOD: A systematic review was undertaken in accordance with PRISMA guidelines. Studies published between 2000 and 2017 describing the clinical management of PRSC in patients with UC within 30 days of primary ileo-anal pouch surgery were included. A qualitative analysis was undertaken due to the heterogeneity and quality of studies included. RESULTS: A total of 1157 abstracts and 266 full text articles were screened. Twelve studies were included for analysis involving a total of 207 patients. The studies described a range of techniques including image-guided, endoscopic, surgical and endocavitational vacuum methods. Based on the evidence from these studies, an algorithm was created to guide the management of early PRSC. CONCLUSION: The results of this review suggest that although successful salvage of early PRSC is improving there is little information available relating to methods of salvage and outcomes. Novel techniques may offer an increased chance of salvage but comparative studies with longer follow-up are required.


Asunto(s)
Absceso/terapia , Algoritmos , Fuga Anastomótica/terapia , Colitis Ulcerosa/cirugía , Pelvis , Proctocolectomía Restauradora/efectos adversos , Sepsis/terapia , Absceso/etiología , Fuga Anastomótica/etiología , Drenaje/métodos , Humanos , Ileostomía , Reoperación , Sepsis/etiología , Factores de Tiempo , Vacio
4.
Colorectal Dis ; 20(9): 804-812, 2018 09.
Artículo en Inglés | MEDLINE | ID: mdl-29603863

RESUMEN

AIM: A longstanding disparity exists between the approaches to restorative surgery after colectomy for patients with ulcerative colitis (UC) in England and Sweden. This study aims to compare rates of colectomy and restorative surgery in comparable national cohorts. METHOD: The English Hospital Episode Statistics (HES) and Swedish National Patient Register (NPR) were interrogated between 2002 and April 2012. Patients with two diagnostic episodes for UC (age ≥ 15 years) were included. Patients were excluded if they had an episode of inflammatory bowel disease or colectomy before 2002. The cumulative incidences of colectomy and restorative surgery were calculated using the Kaplan-Meier method. RESULTS: A total of 98 691 patients were included in the study, 76 129 in England and 22 562 in Sweden. The 5-year cumulative incidence of all restorative surgery after colectomy in England was 33% vs 46% in Sweden (P-value < 0.001). Of the patients undergoing restorative surgery, 92.3% of English patients had a pouch vs 38.8% in Sweden and 7.7% vs 59.1% respectively had an ileorectal anastomosis (IRA). The 5-year cumulative incidence of colectomy in this study cohort was 13% in England and 6% in Sweden (P-value < 0.001). CONCLUSION: Following colectomy for UC only one-third of English patients and half of Swedish patients underwent restorative surgery. In England nearly all these patients underwent pouches, in Sweden a less significant majority underwent IRAs. It is surprising to demonstrate this discrepancy in a comparable cohort of patients from similar healthcare systems. The causes and consequences of this international variation in management are not fully understood and require further investigation.


Asunto(s)
Colectomía/estadística & datos numéricos , Colitis Ulcerosa/cirugía , Disparidades en Atención de Salud/estadística & datos numéricos , Proctocolectomía Restauradora/estadística & datos numéricos , Sistema de Registros , Adolescente , Adulto , Estudios de Cohortes , Colectomía/métodos , Colitis Ulcerosa/diagnóstico , Inglaterra , Femenino , Humanos , Internacionalidad , Estimación de Kaplan-Meier , Masculino , Persona de Mediana Edad , Evaluación de Necesidades , Proctocolectomía Restauradora/métodos , Pronóstico , Estudios Retrospectivos , Suecia , Resultado del Tratamiento , Adulto Joven
8.
Front Mol Biosci ; 10: 1286890, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-38028550

RESUMEN

Introduction: microRNAs (miRNAs) are small non-coding RNAs that work at the posttranscriptional level to repress gene expression. Several miRNAs are preferentially expressed in skeletal muscle and participate in myogenesis. This research was conducted to alter endogenous miRNA expression in skeletal muscle to promote muscle hypertrophy. Methods: Two experiments were conducted using mimic/agomiR or antagomir technologies to alter miRNA expression and examine changes in myoblast proliferation in vitro (experiment 1) and muscle hypertrophy in vivo (experiment 2). In vitro experiments found that antagomiR-22-3p and mimic-127 increased myoblast proliferation compared to other miRNA treatments or controls. These miRNA treatments, antagomiR-22-3p (ANT22) and agomiR-127 (AGO127), were then used for intramuscular injections in longissimus muscle. Results and discussion: The use of antagomiR or mimic/agomiR treatments down-regulated or up-regulated, respectively, miRNA expression for that miRNA of interest. Expression of predicted target KIF3B mRNA for miR-127 was up-regulated and ACVR2a mRNA was up-regulated for miR-22-3p. ANT22 injection also up-regulated the major regulator of protein synthesis (mTOR). Proteomic analyses identified 11 proteins for AGO127 and 9 proteins for ANT22 that were differentially expressed. Muscle fiber type and cross-sectional area were altered for ANT22 treatments to transition fibers to a more oxidative state. The use of agomiR and antagomir technologies allows us to alter miRNA expression in vitro and in vivo to enhance myoblast proliferation and alter muscle fiber hypertrophy in IUGR lambs during early postnatal growth.

9.
Hernia ; 25(4): 977-984, 2021 08.
Artículo en Inglés | MEDLINE | ID: mdl-33712933

RESUMEN

PURPOSE: The Ventral Hernia Working Group (VHWG) classification of ventral/incisional hernia (IH) was developed by expert consensus in 2010. Subsequently, Kanters et al. have demonstrated the validity of a modified version of the system for predicting short-term outcomes. This study aims to evaluate the modified system for predicting hernia recurrence. METHODS: Patients undergoing IH surgery (defined by OPCS codes) in the England Hospital Episode Statistics (HES) database, from 1997 to 2012, were identified. Baseline demographics at index hernia operation and episodes of further hernia surgery (FHS) were recorded. Risk factors for FHS were identified using cox regression and evaluated against the modified-VHWG grade using receiver-operating characteristics (ROC). RESULTS: The final analysis included 214,082 index IH operations. Of these, 52.6% were female and mean age was 56.59 (SD15.9). An admission for FHS was found in 8.3% cases (17,714 patients). Multi-variate cox regression revealed contaminated hernia (p < 0.0001), pre-existing IBD (p < 0.0001) and hernia comorbidity (p = 0.05) to be significantly related to long-term FHS. Classifying patients using these factors, according to the modified-VHWG classification, revealed that compared to Grade 1, the hazard ratio (HR) of FHS increased in Grade 2 (HR 1.19; p < 0.0001) and further increased in Grade 3 (HR 1.79; p < 0.0001). ROC analysis revealed the area under the curve to be 0.73 (95% CI 0.73-0.74). CONCLUSION: This analysis demonstrates the broad validity of the modified-VHWG classification in discriminating risk for FHS. Inclusion of pre-existing IBD as a factor defining Grade 2 patients would be recommended. This analysis is limited by the absence of certain factors within the HES database, such as BMI.


Asunto(s)
Hernia Ventral , Hernia Incisional , Femenino , Hernia Ventral/epidemiología , Hernia Ventral/cirugía , Herniorrafia/efectos adversos , Hospitales , Humanos , Persona de Mediana Edad , Recurrencia , Estudios Retrospectivos , Factores de Riesgo , Mallas Quirúrgicas
10.
Aliment Pharmacol Ther ; 45(5): 581-592, 2017 03.
Artículo en Inglés | MEDLINE | ID: mdl-28008631

RESUMEN

BACKGROUND: Restorative proctocolectomy with ileal pouch anal anastomosis (IPAA) is considered the procedure of choice in patients with ulcerative colitis (UC) refractory to medical therapy. The incidence of pouchitis is 40% at 5 years. Ten to 15% of patients with pouchitis experience chronic pouchitis. AIM: To determine the efficacy of medical therapies for the treatment of chronic refractory pouchitis in patients undergoing IPAA for UC. METHODS: A systematic computer-assisted search of the on-line bibliographic database MEDLINE and EMBASE was performed between 1966 and February 2016. All original studies reporting remission rates following medical treatment for chronic pouchitis were included. All study designs were considered. Remission was defined according to the individual study. Remission endpoints ranged from 15 days to 10 weeks. Chronic pouchitis was defined by each study. RESULTS: Twenty-one papers were considered eligible. Results from all studies combined suggested that overall remission was obtained in 59% of patients (95% CI: 44-73%). Antibiotics significantly induced remission in patients with chronic pouchitis with 74% remission rate (95% CI:56-93%), (P < 0.001). Biologics significantly induced remission in patients with chronic pouchitis with 53% remission rate (95% CI:30-76%), (P < 0.001). Steroids, bismuth, elemental diet and tacrolimus all can induce remission but failed to achieve significance. Faecal microbiota transplantation in a single study was not found to achieve remission. CONCLUSIONS: Treatment of chronic refractory pouchitis remains difficult and is largely empirical. Larger randomised controlled trials will help aid the management of chronic pouchitis.


Asunto(s)
Colitis Ulcerosa/cirugía , Reservoritis/terapia , Proctocolectomía Restauradora/efectos adversos , Algoritmos , Canal Anal/cirugía , Reservorios Cólicos , Humanos , Reservoritis/etiología , Inducción de Remisión , Tacrolimus/administración & dosificación
11.
J Med Genet ; 42(12): 940-6, 2005 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-15831595

RESUMEN

Neural tube defects (NTDs) are the second most common birth defects (1 in 1000 live births) in the world. Periconceptional maternal folate supplementation reduces NTD risk by 50-70%; however, studies of folate related and other developmental genes in humans have failed to definitively identify a major causal gene for NTD. The aetiology of NTDs remains unknown and both genetic and environmental factors are implicated. We present findings from a microsatellite based screen of 44 multiplex pedigrees ascertained through the NTD Collaborative Group. For the linkage analysis, we defined our phenotype narrowly by considering individuals with a lumbosacral level myelomeningocele as affected, then we expanded the phenotype to include all types of NTDs. Two point parametric analyses were performed using VITESSE and HOMOG. Multipoint parametric and nonparametric analyses were performed using ALLEGRO. Initial results identified chromosomes 7 and 10, both with maximum parametric multipoint lod scores (Mlod) >2.0. Chromosome 7 produced the highest score in the 24 cM interval between D7S3056 and D7S3051 (parametric Mlod 2.45; nonparametric Mlod 1.89). Further investigation demonstrated that results on chromosome 7 were being primarily driven by a single large pedigree (parametric Mlod 2.40). When this family was removed from analysis, chromosome 10 was the most interesting region, with a peak Mlod of 2.25 at D10S1731. Based on mouse human synteny, two candidate genes (Meox2, Twist1) were identified on chromosome 7. A review of public databases revealed three biologically plausible candidates (FGFR2, GFRA1, Pax2) on chromosome 10. The results from this screen provide valuable positional data for prioritisation of candidate gene assessment in future studies of NTDs.


Asunto(s)
Cromosomas Humanos Par 10 , Cromosomas Humanos Par 7 , Ligamiento Genético , Genoma Humano , Cresta Neural/patología , Defectos del Tubo Neural/genética , Salud de la Familia , Femenino , Marcadores Genéticos , Genotipo , Humanos , Masculino , Modelos Genéticos , Linaje , Mapeo Físico de Cromosoma
12.
Pediatrics ; 76(1): 15-21, 1985 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-4040236

RESUMEN

Immunocytochemical study of human brain showed creatine kinase brain isoenzyme (CKBB) present in both neurons and astrocytes. Because creatine kinase brain isoenzyme is an intracellular enzyme that might be released with brain injury, its concentration in the CSF of newborns was measured using a radioimmunoassay. Infants who suffered a documented neurologic insult (a cerebroventricular hemorrhage or a CNS infection) were found to have a greater mean CSF creatine kinase brain isoenzyme concentration than those without a history of neurologic insult. Infants with a high concentration had a poor short-term outcome (death or neurologic abnormality when discharged) more frequently than did those with a lower concentration. Infants with a grade 3 or 4 cerebroventricular hemorrhage had a higher mean concentration than did those with a grade 1 or 2 hemorrhage. These data are consistent with the hypothesis that CSF creatine kinase brain isoenzyme is a metabolic indicator of brain damage in newborns.


Asunto(s)
Encefalopatías/enzimología , Encéfalo/enzimología , Creatina Quinasa/líquido cefalorraquídeo , Enfermedades del Prematuro/enzimología , Astrocitos/enzimología , Hemorragia Cerebral/enzimología , Creatina Quinasa/análisis , Humanos , Lactante , Recién Nacido , Infecciones/enzimología , Isoenzimas , Neuronas/enzimología , Pronóstico , Radioinmunoensayo
13.
Urology ; 39(3): 248-50, 1992 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-1546418

RESUMEN

The records of 181 patients with myelodysplasia were reviewed. The prevalence of associated genitourinary anomalies as well as cardiac, facial, anal, and tethered cord were determined. The prevalence of congenital malformations associated with myelodysplasia were less in this series than in previous reports.


Asunto(s)
Anomalías Múltiples/epidemiología , Defectos del Tubo Neural/complicaciones , Femenino , Humanos , Masculino , Prevalencia
14.
J Pediatr Surg ; 36(9): 1381-6, 2001 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-11528610

RESUMEN

BACKGROUND/PURPOSE: Diagnosis and management of the acute abdomen in patients with spina bifida (SB) can be problematic. There are at least 4 clinical factors that can predispose to the development of acute abdominal symptoms and signs, and patients with a thoracic level lesion can have a partially insensate abdomen. The authors analyzed their accumulated experience to determine the annual incidence of acute abdominal signs and symptoms in children and young adults with spina bifida, the differential diagnosis, the operative management, and the outcome. The pertinent literature was reviewed. METHODS: Cases were ascertained during a 10-year period at 1 institution and reviewed retrospectively. RESULTS: Twenty-two episodes of acute abdominal symptoms and signs in 19 children and young adults with SB were ascertained over 10 years at 1 institution, for an annual incidence of 0.74%. More patients had a thoracic level lesion (n = 12; 60%) than in the clinic population as a whole (27%; P =.04), but the gender distribution was similar (58% girls), as was the prevalence of ventriculoperitoneal shunts (VPS; 95%). The median age was 13 years (range, 1 year to 26 years). Hospitalization was necessary for 19 (86%) of the 22 episodes. The duration of symptoms before diagnosis was a median of 3 days (range, 1 to 14 days). Most patients (82%) presented with abdominal pain. Fever was present in 27%, shock in 23%, and peritoneal signs in 23%. There were 14 different final diagnoses, 10 (71%) of which were associated with a predisposing factor. Of the 22 episodes, 18 (82%) could be attributed to an underlying factor: (1) neurogenic bladder (9; 41%); (2) neurogenic bowel (3; 14%); (3) VPS (4; 18%); (4) complications from previous surgery (2; 9%). Thirteen patients (59%) underwent a total of 20 surgical procedures of 12 different kinds. Despite awareness of the complexities involved, 3 patients (14%) died: 1 from complications resulting from bladder perforation; 1 from urosepsis and shock; and 1 from peritonitis caused by VPS infection. CONCLUSION: The differential diagnosis of the acute abdomen in patients with SB is broad, conditions requiring surgery are frequently diagnosed, and the mortality rate is substantial, despite aggressive management.


Asunto(s)
Abdomen Agudo/diagnóstico , Abdomen Agudo/epidemiología , Disrafia Espinal/epidemiología , Adolescente , Adulto , Distribución por Edad , Niño , Preescolar , Comorbilidad , Femenino , Humanos , Incidencia , Masculino , Pronóstico , Medición de Riesgo , Factores de Riesgo , Distribución por Sexo , Disrafia Espinal/diagnóstico , Disrafia Espinal/cirugía
15.
Int J Pediatr Otorhinolaryngol ; 51(2): 109-13, 1999 Dec 05.
Artículo en Inglés | MEDLINE | ID: mdl-10619624

RESUMEN

Effective adjuvant treatment for recurrent respiratory papillomatosis (RRP) is at present limited to alpha-interferon, which may have significant side effects including rebound growth of papillomata following its withdrawal, is given by injection and is expensive. High dose cimetidine is known to have immunomodulatory side effects and has been reported as a useful treatment for cutaneous warts. We report a case of very advanced RRP with tracheo-bronchial-pulmonary involvement treated with adjuvant cimetidine at a dose of 40 mg/kg for 4 months. The patient enjoyed a remarkable improvement in her clinical condition following treatment. The literature regarding cimetidine treatment for cutaneous warts is reviewed.


Asunto(s)
Adyuvantes Inmunológicos/uso terapéutico , Neoplasias de los Bronquios/tratamiento farmacológico , Cimetidina/uso terapéutico , Neoplasias Pulmonares/tratamiento farmacológico , Recurrencia Local de Neoplasia/tratamiento farmacológico , Papiloma/tratamiento farmacológico , Neoplasias de la Tráquea/tratamiento farmacológico , Adyuvantes Inmunológicos/administración & dosificación , Niño , Femenino , Estudios de Seguimiento , Humanos , Interferón-alfa/efectos adversos , Interferón-alfa/uso terapéutico , Inducción de Remisión
16.
Clin Pediatr (Phila) ; 37(6): 347-52, 1998 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-9637898

RESUMEN

Hypophosphatemia in malnourished children during nutritional recovery (refeeding hypophosphatemia) is recognized as a cause of morbidity and mortality in adolescents with anorexia nervosa but has been only rarely reported to occur in younger children with other diagnoses. Over a 6-year period, we encountered three cases of refeeding hypophosphatemia in malnourished children admitted to a pediatric rehabilitation hospital. Two children had neurologic dysphagia and one had been starved by an abusive parent. The one patient who was symptomatic had obtundation, hemolytic anemia, rhabdomyolysis, and hepatocellular injury that began during refeeding and resolved with treatment. The signs and symptoms, pathophysiology, and treatment of refeeding hypophosphatemia are reviewed.


Asunto(s)
Nutrición Enteral/métodos , Hipofosfatemia/etiología , Desnutrición Proteico-Calórica/sangre , Niño , Preescolar , Métodos de Alimentación , Femenino , Gastrostomía , Humanos , Hipofosfatemia/terapia , Masculino , Fósforo/sangre , Desnutrición Proteico-Calórica/terapia
17.
Clin Pediatr (Phila) ; 40(5): 249-52, 2001 May.
Artículo en Inglés | MEDLINE | ID: mdl-11388673

RESUMEN

Ninety-three individuals with Down syndrome (DS) were screened to investigate the prevalence of celiac disease (CD) in the United States. Five of the 93 individuals were antiendomysial antibody (EMA) positive. Of the 5 who tested positive for EMA, 4 were biopsied, 1 refused biopsy. Three of the 4 individuals biopsied manifested changes of CD on small bowel biopsy. This gives a frequency of 3.2% of confirmed CD in our DS individuals and suggests the need for periodic screening for celiac disease in this population.


Asunto(s)
Algoritmos , Enfermedad Celíaca/epidemiología , Tamizaje Masivo/métodos , Adolescente , Adulto , Autoanticuerpos/sangre , Biopsia , Enfermedad Celíaca/diagnóstico , Enfermedad Celíaca/etiología , Niño , Preescolar , Síndrome de Down/complicaciones , Síndrome de Down/inmunología , Femenino , Gliadina/inmunología , Humanos , Inmunoglobulina A/sangre , Inmunoglobulina G/sangre , Lactante , Masculino , Fibras Musculares Esqueléticas/inmunología , Prevalencia , Estudios Prospectivos , Estados Unidos/epidemiología
18.
Rhinology ; 39(3): 125-7, 2001 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-11721500

RESUMEN

An effective system for scoring pathological changes on CT scans of the paranasal sinuses has been developed by Lund & Mackay. We have performed an audit using 100 outpatients with nasal symptoms and found that adherence to guidelines prior to ordering CT scans of the paranasal sinuses correlates with an increased average Lund & Mackay score. Using these guidelines has also reduced the number of inappropriate CT scan requests.


Asunto(s)
Enfermedades de los Senos Paranasales/diagnóstico por imagen , Guías de Práctica Clínica como Asunto , Tomografía Computarizada por Rayos X , Humanos , Enfermedades de los Senos Paranasales/clasificación , Tomografía Computarizada por Rayos X/estadística & datos numéricos
19.
J Laryngol Otol ; 112(9): 870-1, 1998 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-9876380

RESUMEN

Pyoderma gangrenosum affecting the nose is rare and this may lead to diagnostic confusion because of the large differential diagnosis. As diagnosis is made, largely, on the basis of exclusion the treatment of pyoderma gangrenosum may be unduly delayed. The condition is often disfiguring, particularly following inappropriate surgical intervention, and early diagnosis is therefore important. We present a case of pyoderma gangrenosum managed initially in the community with minor surgery and resulting in the rare complication of saddle nose deformity.


Asunto(s)
Colitis Ulcerosa/complicaciones , Deformidades Adquiridas Nasales/etiología , Piodermia Gangrenosa/complicaciones , Anciano , Colitis Ulcerosa/patología , Femenino , Humanos , Nariz/patología , Deformidades Adquiridas Nasales/patología , Piodermia Gangrenosa/patología , Pulgar/patología
20.
J Laryngol Otol ; 113(9): 841-3, 1999 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-10664690

RESUMEN

Branchio-oto-renal syndrome is a rare autosomal dominant condition characterized by hearing loss, branchial arch abnormalities and renal tract malformations. We present the first reported case of branchio-oto-renal syndrome associated with bilateral congenital cholesteatoma and ossicular chain abnormalities. The pathogenesis of this syndrome is described and the literature is reviewed.


Asunto(s)
Síndrome Branquio Oto Renal/complicaciones , Colesteatoma del Oído Medio/congénito , Colesteatoma del Oído Medio/complicaciones , Osículos del Oído/anomalías , Pérdida Auditiva Bilateral/etiología , Síndrome Branquio Oto Renal/diagnóstico por imagen , Colesteatoma del Oído Medio/diagnóstico por imagen , Femenino , Pérdida Auditiva Bilateral/diagnóstico por imagen , Humanos , Lactante , Tomografía Computarizada por Rayos X
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