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1.
Rev. chil. radiol ; 24(4): 151-154, dic. 2018. ilus
Article in Spanish | LILACS | ID: biblio-978171

ABSTRACT

El dolor torácico es un motivo frecuente de consulta en los servicios de urgencias, sin embargo, el hematoma esofágico es una causa muy poco frecuente. Se manifiesta más frecuentemente en mujeres de edad media y avanzada, con una triada de dolor torácico súbito, disfagia u odinofagia y hematemesis. Presentamos un caso de una mujer de 89 años con antecedentes de hipertensión arterial en tratamiento, usuaria de antihipertensivos y aspirina, con una historia de dos días de evolución de dolor retroesternal, sensación febril, disnea y tos productiva secundario a un hematoma esofágico.


Thoracic pain is a frequent reason for consultation in the emergency department, however, esophageal hematoma is a very rare cause. It manifests more commonly in women of middle and advanced age, with a triad of sudden chest pain, dysphagia or odynophagia and hematemesis. We present a case of a 89 years old female patient, with a history of arterial hypertension in treatment, user of antihypertensive drugs and aspirin with a two day history of retrosternal pain, febrile sensation, dyspnea and productive cough due to a esophageal hematoma.


Subject(s)
Humans , Female , Aged, 80 and over , Esophageal Diseases/diagnostic imaging , Hematoma/diagnostic imaging , Chest Pain/etiology , Radiography, Thoracic , Tomography, X-Ray Computed , Esophageal Diseases/etiology
2.
J. bras. nefrol ; 40(3): 266-272, July-Sept. 2018. tab
Article in English | LILACS | ID: biblio-975906

ABSTRACT

ABSTRACT Introduction: The incidence of gastrointestinal disorders among patients with chronic kidney disease (CKD) is high, despite the lack of a good correlation between endoscopic findings and symptoms. Many services thus perform upper gastrointestinal (UGI) endoscopy on kidney transplant candidates. Objectives: This study aims to describe the alterations seen on the upper endoscopies of 96 kidney-transplant candidates seen from 2014 to 2015. Methods: Ninety-six CKD patients underwent upper endoscopic examination as part of the preparation to receive kidney grafts. The data collected from the patients' medical records were charted on Microsoft Office Excel 2016 and presented descriptively. Mean values, medians, interquartile ranges and 95% confidence intervals of the clinic and epidemiological variables were calculated. Possible associations between endoscopic findings and infection by H. pylori were studied. Results: Males accounted for 54.17% of the 96 patients included in the study. Median age and time on dialysis were 50 years and 50 months, respectively. The most frequent upper endoscopy finding was enanthematous pangastritis (57.30%), followed by erosive esophagitis (30.20%). Gastric intestinal metaplasia and peptic ulcer were found in 8.33% and 7.30% of the patients, respectively. H. pylori tests were positive in 49 patients, and H. pylori infection was correlated only with non-erosive esophagitis (P = 0.046). Conclusion: Abnormal upper endoscopy findings were detected in all studied patients. This study suggested that upper endoscopy is a valid procedure for kidney transplant candidates. However, prospective studies are needed to shed more light on this matter.


RESUMO Introdução: A incidência de doenças gastrointestinais altas em pacientes com doença renal crônica é elevada, porém não há boa correlação entre achados endoscópicos e sintomas. Assim, muitos serviços preconizam a realização de Endoscopia Digestiva Alta (EDA) nos candidatos a transplante renal. Objetivos: Descrever alterações endoscópicas presentes em 96 candidatos a transplante renal no período de 2014 a 2015. Métodos: Noventa e seis pacientes renais crônicos submetidos à EDA como preparo para transplante renal. Prontuários médicos dos pacientes foram revisados, os dados tabulados no programa Microsoft Office Excel 2016 e apresentados de maneira descritiva. Calculou-se média, mediana, intervalo interquartílico e intervalo de confiança de 95% das variáveis utilizadas. Alterações endoscópicas foram apresentadas quanto ao número, intervalo de confiança e valor de P, e correlacionadas com a presença ou ausência de infecção por Helicobacter pylori. Resultados: Dos 96 pacientes, 54,17% eram homens e 45,83% mulheres. As medianas de idade e tempo em diálise foram 50 anos e 50 meses, respectivamente. O achado mais comum na EDA foi pangastrite enantematosa (57,30%), seguida de esofagite erosiva (30,20%). Metaplasia intestinal gástrica e úlcera péptica foram encontradas em 8,33% e 7,30% dos pacientes, respectivamente. Pesquisa para H. pylori foi positiva em 49 pacientes, e somente houve correlação entre infecção por H. pylori e esofagite não erosiva (P = 0,046). Conclusão: Afecções gastrointestinais foram detectadas em todos os pacientes estudados. Os achados deste estudo sugerem que a realização de EDA em candidatos a receber transplante renal é desejável. Entretanto, estudos prospectivos são necessários para responder a esta questão.


Subject(s)
Humans , Male , Female , Adult , Middle Aged , Stomach Diseases/etiology , Duodenal Diseases/etiology , Esophageal Diseases/etiology , Renal Insufficiency, Chronic/complications , Stomach Diseases/diagnosis , Cross-Sectional Studies , Endoscopy, Gastrointestinal , Kidney Transplantation , Duodenal Diseases/diagnosis , Esophageal Diseases/diagnosis , Renal Insufficiency, Chronic/surgery
3.
Arch. argent. pediatr ; 116(2): 315-318, abr. 2018. ilus
Article in English, Spanish | LILACS, BINACIS | ID: biblio-887477

ABSTRACT

La gastrostomía endoscópica percutánea (GEP) se utiliza como alternativa de la alimentación enteral/nasoenteral en situaciones en las que la alimentación por vía oral a largo plazo no es eficaz o no se tolera. Se prefiere principalmente en pacientes con afecciones neurológicas y, además, como apoyo de la nutrición en pacientes con enfermedades cardíacas congénitas, fibrosis quística, enfermedad intestinal inflamatoria y diversas enfermedades orofaríngeas. Si bien la colocación es sencilla en comparación con muchos procedimientos invasivos, presenta complicaciones, que incluyen desde la infección de la herida hasta la muerte. La GEP exige personal médico experimentado, antibióticos profilácticos adecuados e información exhaustiva para los pacientes o sus familias sobre el procedimiento y los cuidados posteriores. Presentamos una complicación rara, aunque importante, que surgió durante el reemplazo de la sonda de gastrostomía después del método de "corte y empuje". El tope, que debe llegar hasta el extremo distal del estómago, se desplazó hacia arriba, hasta el esófago proximal, y causó una úlcera profunda en la mucosa esofágica y una hemorragia masiva.


Percutaneous endoscopic gastrostomy (PEG) is used as an alternative to enteral/nasoenteral feeding in situations where long-term oral feeding is ineffective or not tolerated. It is mostly preferred in patients with neurological conditions and also to support nutrition in patients with congenital heart diseases, cystic fibrosis, inflammatory bowel disease, and various oropharyngeal diseases. Although it is easily applicable compared to many invasive procedures, it has complications ranging from wound infection to death. PEG requires experienced medical personnel, appropriate prophylactic antibiotics and exhaustive information to the patients or their families about the procedure and subsequent care. We present a rare but important complication during the replacement of the gastrostomy tube subsequent to the "cut and push" method. The bumper portions, which should move to the distal end of the stomach, moved upwards to the proximal esophagus, caused a deep ulcer in the esophageal mucosa and a massive hemorrhage.


Subject(s)
Humans , Male , Child, Preschool , Postoperative Complications/diagnosis , Gastrostomy/adverse effects , Esophageal Diseases/etiology , Gastrointestinal Hemorrhage/etiology , Gastrostomy/methods , Fatal Outcome , Endoscopy , Esophageal Diseases/diagnosis , Gastrointestinal Hemorrhage/diagnosis
4.
Rev. bras. reumatol ; 57(6): 521-525, Nov.-Dec. 2017. tab
Article in English | LILACS | ID: biblio-899467

ABSTRACT

Abstract Objective: To assess esophageal involvement (EI) in juvenile localized scleroderma (JLS) population and the possible association between this gastrointestinal manifestation and demographic data, clinical features, laboratory exams, treatments and outcomes. Methods: For a period of 30 years, 5881 patients with rheumatic diseases were followed in our Pediatric Rheumatology Division. EI was defined by the presence of symptoms (solid/liquid dysphagia, heartburn, esophageal regurgitation, nausea/vomiting and epigastralgia) and confirmed by at least one EI exam abnormality: barium contrast radiography, upper gastrointestinal endoscopy and 24-hour esophageal pH-monitoring. Results: JLS was observed in 56/5881 patients (0.9%), mainly linear morphea subtype. EI was observed in 23/56(41%) of JLS patients. Eight(35%) of 23 EI patients with JLS were symptomatic and presented heartburn(5/8), solid and liquid dysphagia(3/8), nausea and epigastralgia(1/8). The frequency of any cumulative extracutaneous manifestations (calcinosis, arthritis/arthralgia, central nervous system, interstitial pneumonitis, mesangial nephritis and/or arrhythmia) was significantly higher in JLS patients with EI compared to those without this complication (56% vs. 24%, p = 0.024). No differences were evidenced in demographic data, JLS subtypes and in each extracutaneous manifestation in both groups (p > 0.05). The frequency of methotrexate use was significantly higher in JLS patients with EI compared to those without (52% vs. 12%, p = 0.002). Autoantibody profile (antinuclear antibodies, anti-SCL-70, rheumatoid factor, anticentromere, anti-cardiolipin, anti-Ro/SSA and anti-La/SSB) was similar in both groups (p > 0.05). Conclusions: Our study demonstrated that EI was frequently observed in JLS patients, mainly in asymptomatic patients with linear subtype. EI occurred in JLS patients with other extracutaneous manifestations and required methotrexate therapy.


Resumo Objetivo: Avaliar o envolvimento do esôfago (EE) na população com esclerodermia localizada juvenil (ELJ) e a possível associação entre essa manifestação gastrointestinal e dados demográficos, características clínicas, exames laboratoriais, tratamentos e desfechos. Métodos: Durante 31 anos, 5.881 pacientes com doenças reumáticas foram acompanhados em nossa Divisão de Reumatologia Pediátrica. O EE foi definido pela presença de sintomas (disfagia para sólidos/líquidos, azia, regurgitação esofágica, náuseas/vômitos e epigastralgia) e confirmado com pelo menos um exame que revelou EE: radiografia contrastada com bário, endoscopia digestiva alta e pHmetria esofágica de 24 horas. Resultados: Observou-se ELJ em 56/5.881 pacientes (0,9%), principalmente do subtipo morfeia linear. O EE foi observado em 23/56 (41%) dos pacientes com ELJ. Oito (35%) dos 23 pacientes com ELJ com EE eram sintomáticos e apresentavam azia (5/8), disfagia para sólidos e líquidos (3/8), náuseas e epigastralgias (1/8). A frequência de quaisquer manifestações extracutâneas cumulativas (calcinose, artrite/artralgia, envolvimento do sistema nervoso central, pneumonite intersticial, nefrite mesangial e/ou arritmias) foi significativamente maior em pacientes com ELJ com EE em comparação com aqueles sem essa complicação (56% vs. 24%, p = 0,024). Não foi evidenciada diferença nos dados demográficos, subtipos de ELJ e quaisquer manifestações extracutâneas entre os grupos (p > 0,05). A frequência de uso de metotrexato foi significativamente maior em pacientes com ELJ com EE em comparação com aqueles sem EE (52% vs. 12%, p = 0,002). O perfil de autoanticorpos (anticorpos antinucleares, anti-SCL-70, fator reumatoide, anticentrômero, anticardiolipina, anti-Ro/SSA e anti-La/SSB) foi semelhante nos dois grupos (p > 0,05). Conclusões: Este estudo demonstrou que o EE foi frequentemente observado em pacientes com ELJ, principalmente naqueles assintomáticos com o subtipo linear da doença. O EE ocorreu em pacientes com ELJ com outras manifestações extracutâneas e exigiu tratamento com metotrexato.


Subject(s)
Humans , Male , Female , Child, Preschool , Child , Scleroderma, Localized/complications , Esophageal Diseases/etiology , Scleroderma, Localized/drug therapy , Methotrexate/therapeutic use , Retrospective Studies , Endoscopy, Gastrointestinal , Antirheumatic Agents/therapeutic use
5.
Int. braz. j. urol ; 42(3): 594-602, tab, graf
Article in English | LILACS | ID: lil-785722

ABSTRACT

ABSTRACT The co-occurrence of multiple pathologies in the pelvic viscera in the same patient, such as, irritable bowel syndrome and interstitial cystitis, indicates the complexity of viscero-visceral interactions and the necessity to study these interactions under multiple pathological conditions. In the present study, the effect of distal colon irritation (DCI) on the urinary bladder interaction with distal esophagus distention (DED), distal colon distention (DCD), and electrical stimulation of the abdominal branches of vagus nerve (abd-vagus) were investigated using cystometry parameters. The DCI significantly decreased the intercontraction time (ICT) by decreasing the storage time (ST); nonetheless, DED and Abd-vagus were still able to significantly decrease the ICT and ST following DCI. However, DCD had no effect on ICT following the DCI. The DCI, also, significantly decreased the Intravesical pressure amplitude (P-amplitude) by increasing the resting pressure (RP). Although DED has no effect on the P-amplitude, both in the intact and the irritated animals, the abd-vagus significantly increased the P-amplitude following DCI by increasing the maximum pressure (MP). In the contrary, 3mL DCD significantly increased the P-amplitude by increasing the MP and lost that effect following the DCI. Concerning the pressure threshold (PT), none of the stimuli had any significant changes in the intact animals. However, DCI significantly decreased the PT, also, the abd-vagus and 3mL DCD significantly decreased the PT. The results of this study indicate that chemical irritation of colon complicates the effects of mechanical irritation of esophagus and colon on urinary bladder function.


Subject(s)
Animals , Male , Female , Urinary Bladder/physiopathology , Colonic Diseases/physiopathology , Irritable Bowel Syndrome/physiopathology , Esophageal Diseases/physiopathology , Pressure , Reference Values , Time Factors , Vagus Nerve/physiopathology , Urinary Bladder Diseases/etiology , Urinary Bladder Diseases/physiopathology , Viscera/physiopathology , Viscera/innervation , Rats, Wistar , Colon/physiopathology , Colon/innervation , Colonic Diseases/etiology , Irritable Bowel Syndrome/complications , Electric Stimulation , Esophageal Diseases/etiology , Esophagus/physiopathology , Esophagus/innervation
6.
Rev. otorrinolaringol. cir. cabeza cuello ; 70(3): 237-244, dic. 2010. ilus
Article in Spanish | LILACS | ID: lil-577249

ABSTRACT

Se presenta el caso de un paciente de 67 años de sexo masculino, hipertenso, diabético y usuario de aspirina en dosis anticoagulante, que consulta en el servicio de urgencia por un cuadro de inicio súbito de dolor retroesternal asociado a disnea severa y estridor. La evaluación mediante nasofibroscopfa muestra una gran masa supraglótica que obstruye el 80 por ciento del lumen, compatible con una masa esofágica. La tomograffa computarizada de tórax muestra una imagen compatible con un hematoma disecante esofágico de gran extensión, desde laringe hasta la unión gastroesofágica. El paciente se maneja en forma conservadora mediante observación, analgesia y alimentación párenteral. Se evalúa en forma periódica con tomograffa computarizada y nasofibroscopfa. Evoluciona con reabsorción progresiva del hematoma y disminución del compromiso laríngeo por lo que es dado de alta a los 10 días. Este caso ejemplifica una rara patología que además tiene una forma atípica de presentación, con obstrucción laríngea.


We present a case of a 67 years old hipertense and diabetic male. The patient refered a sudden onset of chest pain associated with severe dysnea and audible stridor. Nasofibroscopy showed a supraglottic mass that obstructed an estimated 80 percent of normal lumen, suggestive of an esophageal mass. Thorax CT scan revealed an ¡mage of a dissecting esophageal haematoma that compromised most of the esophageal extension, beggining at the laryngeal plane. The patient was managed by conservative means, through observation, analgesia and parenteral nutrition. Close follow up, by CT Scan as well as nasofibroscopy. The patient evolved well, with haematoma reabsorption and decrease of laryngeal obstruction being discharged after 10 days of hospitalization. We report a rare entity that presented in an unusual way.


Subject(s)
Humans , Male , Aged , Esophageal Diseases/surgery , Esophageal Diseases , Hematoma/surgery , Hematoma , Diagnosis, Differential , Esophageal Diseases/etiology , Hematoma/etiology , Laryngoscopy/methods , Tomography, X-Ray Computed
7.
Arq. gastroenterol ; 46(4): 279-283, out.-dez. 2009. tab
Article in English | LILACS | ID: lil-539621

ABSTRACT

Context: Although endoscopic esophageal variceal sclerotherapy has been largely supplanted by variceal band ligation, it is still performed routinely in many institutions, especially in developing countries. Intramural esophageal hematoma has been described as a rare complication of sclerotherapy. Risk factors have not been completely established. Objective: To demonstrate the incidence of post-sclerotherapy intramural esophageal hematoma in our hospital and discuss the possible factors involved. Methods - This is a retrospective observational study made at the "Hospital Universitário Clementino Fraga Filho", Rio de Janeiro, RJ, Brazil, reviewing the medical records of all esophageal variceal sclerotherapy procedures performed from April 2000 to November 2005. The evaluation of the clinical, laboratorial and endoscopic features in our patients and those reported in the literature was also done. Review of literature was performed through MEDLINE search. Results: A total of 1,433 esophageal variceal sclerotherapy procedures were performed in 397 patients, with an intramural esophageal hematoma incidence of 4 cases (0.28 percent). Three of our patients developed additional complications, and one death was a direct consequence of a rupture of the hematoma. Nineteen well described cases were reported in the literature. Intramural esophageal hematoma occurred mostly after the forth esophageal variceal sclerotherapy session. Coagulation disturbances were present in the majority of cases. Conclusion: Intramural esophageal hematoma is a rare complication of esophageal variceal sclerotherapy and its incidence in our institution was similar to those observed in the literature. Our study suggests that this complication occurs as a result of a fragile esophageal mucosa after previous esophageal variceal sclerotherapy sessions. Impaired coagulation, although not essential, could contribute to hematoma formation and extension through esophageal submucosa.


Contexto: Apesar do fato de que a escleroterapia endoscópica de varizes esofágicas vem sendo largamente substituída pela técnica de ligadura elástica, a escleroterapia é ainda rotineiramente utilizada em muitas instituições, especialmente em países em desenvolvimento. O hematoma intramural esofágico é uma complicação rara da escleroterapia e os fatores de risco para seu desenvolvimento ainda não estão completamente estabelecidos. Objetivo - Demonstrar a incidência do hematoma intramural esofágico pós-escleroterapia no Hospital Universitário Clementino Fraga Filho, Rio de Janeiro, RJ, e discutir os possíveis fatores envolvidos. Métodos: Este é um estudo retrospectivo observacional realizado no Hospital Universitário Clementino Fraga Filho, através da revisão dos prontuários médicos de todos os pacientes submetidos a escleroterapia endoscópica de varizes esofágicas entre abril de 2000 e novembro de 2005. Uma avaliação das características clínicas, laboratoriais e endoscópicas desses pacientes e dos descritos na literatura foi realizada. A revisão da literatura foi feita através de pesquisa no MEDLINE. Resultados: Foram realizados 1.433 procedimentos de escleroterapia endoscópica de varizes esofágicas em 397 pacientes, com incidência de hematoma intramural esofágico de 4 casos (0,28 por cento). Três dos quatro pacientes desenvolveram complicações adicionais e um falecimento foi consequência direta do hematoma intramural esofágico. Dezenove casos bem documentados de hematoma intramural esofágico foram descritos na literatura. Na maioria dos casos o hematoma intramural esofágico ocorreu a partir da quarta sessão de escleroterapia endoscópica de varizes esofágicas e distúrbios de coagulação estavam presentes. Conclusão: O hematoma intramural esofágico é complicação rara da escleroterapia e a incidência no hospital onde foi realizada esta pesquisa foi similar à observada na literatura. Este estudo sugere que essa complicação resulta de mucosa...


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Esophageal Diseases/etiology , Esophageal and Gastric Varices/therapy , Hematoma/etiology , Sclerotherapy/adverse effects , Esophagoscopy , Incidence , Retrospective Studies , Sclerotherapy/methods
8.
Arq. bras. cardiol ; 91(6): e53-e55, dez. 2008. ilus
Article in English, Portuguese | LILACS | ID: lil-501802

ABSTRACT

Apresentamos o caso de uma paciente portadora de aneurisma de aorta descendente com ruptura para o esôfago que, após aortoplastia com interposição de tubo de dacron e rafia da laceração esofágica, evoluiu com fístula esôfago pleural no terceiro dia pós-operatório. A paciente necessitou de reintervenção e cuidados intensivos, reabilitando-se adequadamente. A propósito deste caso incomum e do aprendizado adquirido no seu manejo, revisamos a literatura a fim de discutir a melhor alternativa de correção desta rara e, freqüentemente, fatal forma de apresentação das doenças da aorta.


We present the case of a patient with a descending aorta aneurysm rupture into the esophagus, which, after aortoplasty with Dacron tube interposition and suture of esophageal laceration, developed a pleural-esophagus fistula on the 3rd postoperative day. She needed re-intervention and intensive care, followed by adequate recovery. Considering this unusual case and the knowledge acquired through its management, we reviewed the literature in order to discuss the best alternative for the correction of this rare and often fatal form of presentation of aortic diseases.


Subject(s)
Female , Humans , Middle Aged , Aortic Aneurysm, Thoracic/complications , Aortic Rupture/complications , Esophageal Diseases/etiology , Esophageal Fistula/etiology , Vascular Fistula/etiology , Aortic Aneurysm, Thoracic/surgery , Blood Vessel Prosthesis Implantation/adverse effects , Reoperation
9.
Rev. bras. otorrinolaringol ; 74(5): 657-661, set.-out. 2008. ilus, tab
Article in English, Portuguese | LILACS | ID: lil-499837

ABSTRACT

Epidermólise bolhosa (EB) é um conjunto de afecções bolhosas, de caráter hereditário, com diferentes quadros clínicos e diferentes modos de transmissão genética. Os indivíduos evoluem com bolhas na pele e mucosas, que surgem espontaneamente ou após mínimos traumatismos. OBJETIVO: Descrever as manifestações otorrinolaringológicas, as complicações esofágicas relacionadas à EB e a experiência na conduta de pacientes com estenose esofágica decorrente da EB. CASUÍSTICA E MÉTODO: Estudo descritivo de 60 pacientes com EB, atendidos de 1999 a 2006, no serviço de Otorrinolaringologia e Cirurgia de Cabeça e Pescoço do Hospital X, centro de referência para EB. RESULTADOS: Dos 60 pacientes com idade média de 14,5 anos, 28 (46,6 por cento) eram mulheres e 32 (53,4 por cento) homens. Oito (13,4 por cento) tinham o diagnóstico de EB simples, 51 (85 por cento) EB distrófica e um (1,6 por cento) caso de EB adquirida. Lábios, boca, língua e pavilhão auricular foram os locais mais acometidos (32 pacientes - 53,3 por cento). Disfagia foi encontrada em 28 pacientes (46,6 por cento). Após dilatação do esôfago todos apresentaram remissão do sintoma. CONCLUSÃO: EB é uma doença rara e os pacientes devem ser encaminhados para tratamento em centros de referência. Portanto, é fundamental que os médicos envolvidos com os cuidados de pacientes com EB conheçam as condutas necessárias para melhorar a qualidade do tratamento sem prejuízos adicionais.


Epidermolysis bullosa (EB) is a group of skin diseases with different clinical manifestations and varied inheritance patterns. Blisters may appear spontaneously or following minimal trauma to the skin or mucosa. AIM: this paper aims to describe the otorhinolaryngological manifestations and esophageal complications related to EB, and the experience in treating patients with esophageal stenosis secondary to this disease. MATERIALS AND METHOD: this descriptive study enrolled 60 patients with EB seen from June 1999 to December 2006 at the Head and Neck Surgery Service of X Hospital, a reference center for EB. RESULTS: the patients' mean age was 14.5 years. Twenty-eight (46.6 percent) were females and 32 (53.4 percent) were males. Eight (13.4 percent) were diagnosed with epidermolysis bullosa simplex, while 51 (85 percent) had epidermolysis bullosa dystrophica; one (1.6 percent) patient had one acquired EB. Lips, mouth, tongue and ears were the most frequently involved sites (32 patients - 53.3 percent). Dysphagia was found in 28 patients (46.6 percent). After esophageal dilatation the symptoms subsided. CONCLUSION: EB is a rare disease and patients must be sent for treatment at reference centers. Physicians treating patients for EB must be aware of the measures required to improve the quality of the treatment provided without putting the patients in harm's way.


Subject(s)
Adolescent , Child , Child, Preschool , Female , Humans , Infant , Infant, Newborn , Male , Young Adult , Epidermolysis Bullosa/complications , Esophageal Diseases/etiology , Otorhinolaryngologic Diseases/etiology , Case-Control Studies , Deglutition Disorders/etiology , Epidermolysis Bullosa Dystrophica/complications , Epidermolysis Bullosa Dystrophica/therapy , Epidermolysis Bullosa Simplex/complications , Epidermolysis Bullosa Simplex/therapy , Epidermolysis Bullosa/therapy , Esophageal Diseases/therapy , Young Adult
11.
J. bras. pneumol ; 33(4): 480-483, jul.-ago. 2007. ilus
Article in Portuguese | LILACS | ID: lil-466356

ABSTRACT

A ruptura pós-emética do esôfago, também chamada ruptura espontânea ou síndrome de Boerhaave, foi descrita pela primeira vez em 1724 por Herman Boerhaave. Trata-se de uma doença grave, de alta mortalidade e de difícil diagnóstico, tanto por ser rara como por ser freqüentemente confundida com quadros graves mais comuns, como o infarto agudo do miocárdio, a úlcera péptica perfurada e a pancreatite aguda. Descrevemos, a seguir, três casos de pacientes com esta síndrome. Dois foram submetidos ao reparo primário da lesão e um foi submetido à esofagectomia com posterior reconstrução. Houve um óbito por choque séptico no pós-operatório imediato. Os outros dois casos tiveram boa evolução a longo prazo.


Postemetic rupture of the esophagus, also known as spontaneous rupture or Boerhaave's syndrome, was first described by Herman Boerhaave in 1724. This is a severe disease that causes high mortality rates and is difficult to diagnose not only because it is rare but also because it is frequently confused with other severe clinical conditions, such as acute myocardial infarction, perforated peptic ulcer, and acute pancreatitis. Herein, we describe three cases of patients with this syndrome. Two underwent primary repair of the rupture, and one underwent esophagectomy followed by reconstruction. There was one death due to septic shock in the immediate postoperative period. The other two patients presented favorable long-term evolution.


Subject(s)
Adult , Aged , Humans , Male , Middle Aged , Esophageal Diseases/etiology , Vomiting/complications , Esophagectomy , Esophageal Diseases , Esophageal Diseases/surgery , Fatal Outcome , Hydrothorax/etiology , Hydrothorax , Pleural Effusion/etiology , Pleural Effusion , Reoperation , Rupture, Spontaneous/etiology , Rupture, Spontaneous , Rupture, Spontaneous/surgery , Syndrome
12.
Braz. j. infect. dis ; 11(2): 293-296, Apr. 2007. ilus
Article in English | LILACS | ID: lil-454732

ABSTRACT

The involvement of the esophagus in tuberculosis (TB) is extremely rare. This is a case report of an immunocompetent male patient, who presented ganglionary TB reactivation, with the development of extensive esophageal ulcers. The endoscopic approach made the diagnosis possible and there was a total resolution of the symptoms after the treatment.


Subject(s)
Adult , Humans , Male , Esophageal Diseases/etiology , Tuberculosis, Gastrointestinal/complications , Ulcer/etiology , Antitubercular Agents/therapeutic use , Deglutition Disorders/etiology , Esophageal Diseases/diagnosis , Tuberculosis, Gastrointestinal/diagnosis , Tuberculosis, Gastrointestinal/drug therapy , Ulcer/diagnosis
13.
Article in English | IMSEAR | ID: sea-65778

ABSTRACT

Perforation of stasis ulcers in achalasia cardia has not been reported in literature. We report a 45-year-old lady with achalasia and rheumatoid arthritis who developed perforation and esophago-mediastinal sinus at the site of stasis ulcers. She succumbed to respiratory infection after resection of the sinus tract, Heller's cardiomyotomy, cervical esophagostomy and feeding jejunostomy.


Subject(s)
Arthritis, Rheumatoid/complications , Esophageal Achalasia/complications , Esophageal Diseases/etiology , Esophageal Sphincter, Lower/injuries , Esophagostomy , Female , Humans , Jejunostomy , Middle Aged , Reoperation , Rupture, Spontaneous/diagnosis , Ulcer/complications
14.
Article in English | IMSEAR | ID: sea-64230

ABSTRACT

Devascularization surgery for portal hypertension, indicated in selected patients, is considered safe. A 15-year-old boy with cirrhosis underwent elective modified Sugiura's devascularization procedure for secondary prophylaxis of variceal bleeding. He developed esophago-gastric dissociation, which was successfully managed with emergency feeding jejunostomy and restoration of gut continuity three months later.


Subject(s)
Adolescent , Esophageal Diseases/etiology , Esophageal and Gastric Varices/prevention & control , Gastrointestinal Hemorrhage/prevention & control , Humans , Hypertension, Portal/surgery , Male , Postoperative Complications/etiology , Stomach Diseases/etiology , Sutures
15.
Article in English | IMSEAR | ID: sea-125055

ABSTRACT

An oesophageal mucosal bridge can occur due to acquired causes and also due to congenital anomalies. A patient with mucosal bridge of the distal oesophagus following sclerotherapy with absolute alcohol is reported.


Subject(s)
Aged , Esophageal Diseases/etiology , Esophageal and Gastric Varices/diagnosis , Esophagoscopy , Esophagus/abnormalities , Ethanol/administration & dosage , Follow-Up Studies , Gastrointestinal Hemorrhage/diagnosis , Humans , Male , Mucous Membrane/pathology , Risk Assessment , Sclerosing Solutions/adverse effects , Sclerotherapy/adverse effects
16.
Rev. Soc. Bras. Med. Trop ; 33(2): 191-6, mar.-abr. 2000. tab
Article in Portuguese | LILACS | ID: lil-274351

ABSTRACT

Doze pacientes com idades entre 7 a 12 anos, na forma indeterminada da doença de Chagas, com sorologia e xenodiagnóstico positivos, receberam tratamento específico. Dois pacientes tomaram 7mg/kg de nifurtimox durante 60 e 90 dias e 10 usaram 5-7mg/kg de benznidazol durante 60 dias. A evoluçäo clínica foi verificada através de exame clínico, eletrocardiograma, exame radiológico contrastado do esôfago. Após o tratamento somente uma (8,3 por cento) paciente apresentou todos os exames negativos. Oito deles foram avaliados após oito anos do tratamento e 4 acompanhados durante 20 anos. Sete (58,4 por cento) permaneceram na forma indeterminada e 4 (33,3 por cento) chagásicos progrediram clinicamente para cardiopatia grau II e/ou esofagopatia, apesar do tratamento precoce. Säo necessários estudos com maior número de crianças na fase indeterminada e acompanhamento a longo prazo para se estabelecer a influência do tratamento específico na evoluçäo da doença de Chagas


Subject(s)
Humans , Male , Female , Child , Chagas Disease/drug therapy , Trypanosoma cruzi/drug effects , Chronic Disease , Clinical Evolution , Chagas Disease/complications , Esophageal Diseases/etiology , Chagas Cardiomyopathy/etiology , Nifurtimox/pharmacology , Nifurtimox/therapeutic use , Nitroimidazoles/pharmacology , Nitroimidazoles/therapeutic use
17.
Rev. Fac. Cienc. Méd. (Córdoba) ; 56(2): 27-33, 1999. ilus, tab
Article in Spanish | LILACS | ID: lil-262071

ABSTRACT

Com el objeto de establecer el estado del esófago en relación a la noxa chagásica en la región central de Argentina, estudiándolo en pacientes com Chagas, de diferentes edades, se investigó el tiempo de vaciamiento esófago (T.V.E.) así como su calibre, mediante una prueba radiologica estardardizada. Metodología: Se trabajó sobre una muestra de 87 pacientes com pruebas serológicas positivas para Chagas a los que se practicó TVE, en Hospital Rawson. El estudio se realizó retrospectivamente sobre los registros originales. Se consideró TVE retardado cuando se vió bario retenido en esófago mas allá de 1 minuto desde la ingesta. Como controles se utilizó el estudio de TVE efectuado en Hospital Rawson, a 120 personas com serologías negativas para Chagas. Por outra parte, se estudiaron mustras de esófago obtenidos mediante autopsias de pacientes chagásicos que fallecieron por cardiopatía o por otras causas (cuatro casos) del Hospital San Roque, Córdoba, y se efectuaron estudios mediante técnicas histológicas clásicas e inmunohistoquimicas. El 63 por ciento de los pacientes mostraron TVE retardado, en porcentajes crecientes com la edad. En el grupo control no chagásico, sólo el 3 por ciento furon positivos para TVE retardado. El interrogatorio mostró síntomas de disfunción esofágica en el 35 por ciento de los casos chagásicos. El número de megaesófagos fue bajo (tres), correspondientes al grado II. Los resultados histopatológicos mostraron infiltración de linfocitos T PAS +, en torno a estructuras neurales del plexo de Auerbach, y disminución del número de las mismas, en los tres casos. El músculo se vio conservado, aunque hubo también algunas áreas com infiltración T linfocitaria. Surge de los presentes resultados una alta incidencia de trastornos de la función esofágica en eestos pacientes chagásicos de Argentina (87 casos) reflejada en el TVE retardado, creciente com la edad. No obstante, el número de megaesófagos fue bajo y la dilatación de los mismos de grado 2. En el aspecto histopatológico, los casos estudiados mostraron evidencias compatibles com proceso chagásico. Se interpreta que en la producción de grandes megaesófagos frecuentes en outras regiones chagásicas, es posible que intervengan otros factores, en relación com las patologías geográficas.


Subject(s)
Humans , Male , Female , Infant, Newborn , Infant , Child, Preschool , Child , Adolescent , Adult , Middle Aged , Chagas Disease/complications , Esophageal Diseases/etiology , Esophagus/physiopathology , Argentina , Esophageal Achalasia/etiology , Esophageal Achalasia/physiopathology , Esophagus/pathology , Retrospective Studies , Time Factors
18.
Annals of Saudi Medicine. 1998; 18 (2): 193-194
in English | IMEMR | ID: emr-116435
19.
Cir. & cir ; 65(5): 136-40, sept.-oct. 1997.
Article in Spanish | LILACS | ID: lil-217423

ABSTRACT

Se presenta la experiencia a largo plazo (5 años) con una variante de la transección esofágica en la operación de Sugiura-Futagawa. La variante coloca un surgete continuo en toda la circunferencia de el cilindro mucosos sin abrirlo, que oblitera los plexos varicosos. Fueron operados treinta pacientes, quince del sexo femenino, con edad promedio de 43 años. Veintiséis pacientes en Child-Pugh A y cuatro en B. Dieciocho con cirrosisi hepática, siete con hipertensión idiopática y una fibrosis portal congénita. La mortalidad operatoria fue de 6 por ciento y la recurrencia de hemorragia del 10 por ciento. En un caso se presentó fístula (3 por ciento) y un caso de dehiscencia (3 por ciento) con escape controlado. Un caso de estenosis postoperatoria que requirió dilatación. La frecuencia de fístula y estenosis con la transección propuesta es inferior a la reportada en la literatura de transecciones, con frecuencia equiparable de recurrencia de hemorragia


Subject(s)
Humans , Male , Female , Adult , Middle Aged , Liver Cirrhosis/physiopathology , Esophageal Diseases/etiology , Esophageal Diseases/surgery , Hemorrhage/surgery , Hypertension, Portal/surgery , Esophageal and Gastric Varices/surgery
20.
Arq. bras. cardiol ; 69(2): 125-7, ago. 1997. ilus
Article in Portuguese | LILACS | ID: lil-218493

ABSTRACT

Homem de 72 anos, portador de neoplasia de próstata estágio IV, submetido à osteossíntese da coluna cervical para descompressäo metastática da raiz nervosa, responsável por dor intensa no membro superior direito. Após três meses da internaçäo, apresentou trombose total da veia axilo-subclávia direita, complicaçäo da cateterizaçäo prolongada da veia subclávia direita para controle de septicemia secundária a pneumonia hospitalar. Foi submetido a terapia trombolítica com estreptoquinase por via venosa, no membro superior contra-lateral, na dose de 250.000UI em 15 min, seguida de 100.000UI/h durante cinco dias, com total recanalizaçäo do trombo e reduçäo do edema. Após 24h so término da trombólise, apresentou disfagia a líquidos e o esofagograma mostrou extensa compressäo extrínseca do esôfago, por provável hematoma retroesofágico. Necessitou de nutriçäo enterlal durante três meses, quando ocorreu normalizaçäo da deglutiçäo, reabsorçäo do hematoma retroesofágico e passagem adequada do contraste pelo esôfago. No seguimente evolutivo näo apresentou sequelas da trombose venosa profunda, näo tem disfagia e permaneceu em uso profilático de meias elásticas e heparina de baixo peso molecular.


Subject(s)
Male , Aged , Axillary Vein , Esophageal Diseases/etiology , Fibrinolytic Agents/adverse effects , Hematoma/etiology , Prostatic Neoplasms/surgery , Streptokinase/adverse effects , Subclavian Vein , Thrombosis/drug therapy , Deglutition Disorders/etiology , Postoperative Period , Time Factors
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