Boerhaave Syndrome: An Uncommon Cause of Hydropneumothorax

We report the case of a 52-year-old patient with type 2 diabetes mellitus diagnosed with adenocarcinoma rectum, presenting with the complaint of breathlessness to the emergency department. Chest radiograph done showed a left-sided hydropneumothorax with mediastinal shift to the right side. Tube thoracostomy was done. Pleural fluid was exudative; there was no evidence of malignancy. The patient developed a right-sided pleural effusion; anaerobic bacteria were grown on pleural fluid culture. Computed tomography (CT) of the chest was done in view of the new onset empyema on the right side. The CT showed pneumomediastinum and periesophageal air pockets. Orally administered methylene blue had appeared in the pleural drain confirming the diagnosis. The patient was taken up for feeding jejunostomy and repair of tear was planned for a later date. He succumbed to sepsis due to empyema.

Síndrome de Boerhaave: manejo diagnóstico y terapéutico en el Hospital Regional de Talca / Boerhaave Syndrome: diagnostic and therapeutic management at the Hospital Regional de Talca

Introduction: Boerhaave syndrome is a spontaneous rupture of the esophageal wall caused by a sudden increase in intraesophageal pressure. It represents an incidence of approximately 15% of all esophageal perforations, which do not exceed 3.1 per 1 million inhabitants per year. Objectives: To communicate the clinical presentation and management of patients with this syndrome, as well as to reveal the different options available in our service for its treatment. Methods: Search in the statistical data of the regional Hospital of Talca for patients with a diagnosis of Boerhaave syndrome. Five patients were found. Information was obtained from their clinical records and is presented as a clinical case report with a descriptive analysis of their management. Results: Of the 5 clinical cases presented, a classic clinical presentation can be observed, most of the patients presented with vomiting that later evolved with thoracic and/or epigastric pain, associated with imaging studies suggesting esophageal perforation. Management was surgical in 100% of the cases, applying different techniques described in the literature. Discussion and Conclusion: Boerhaave syndrome is a medical-surgical emergency that requires timely management. In spite of the variety of management and the consequences of each one of them, all the patients had an evolution that allowed them to preserve their lives until nowadays. Keeping a high index of suspicion and choosing the best management will have an impact on morbidity and mortality.

Barogenic perforation of the esophagus: An unusual manifestation / Perforación barogénica del esófago: una presentación inusual

Abstract Introduction: Typically, when esophageal perforation secondary to barotrauma is mentioned as the causal pathophysiological mechanism of perforation, the literature refers to spontaneous esophageal perforation or Boerhaave syndrome as an entity. It involves the longitudinal and transmural rupture of the esophagus (previously healthy) secondary to an abrupt increase in intraluminal esophageal pressure, frequently triggered during vomiting. However, in the medical literature, some reports list mechanisms of barotrauma other than this entity. Case report: A 64-year-old female patient with a history of surgically managed gastric adenocarcinoma (total gastrectomy and esophagoenteral anastomosis) presented with stenosis of the esophagojejunal anastomosis, which required an endoscopic dilatation protocol with a CRETM balloon. The third session of endoscopic dilation was held; in removing the endoscope, we identified a deep esophageal laceration with a 4 cm long perforation at the level of the middle esophagus (8 cm proximal to the dilated anastomosis), suspecting the mechanism of barotrauma as the causal agent. She required urgent transfer to the operating room, where we performed thoracoscopic esophagectomy, broad-spectrum empiric antimicrobial coverage, and enteral nutrition by advanced tube during in-hospital surveillance. The control esophagram at seven days showed a small leak over the anastomotic area, which was managed conservatively. Imaging control at 14 days showed a decrease in the size of the leak, with good evolution and tolerance to the oral route. The patient was later discharged.

Resumen Introducción: típicamente, cuando se menciona la perforación esofágica secundaria a barotrauma como el mecanismo fisiopatológico causal de la perforación, la literatura se refiere a la perforación esofágica espontánea o síndrome de Boerhaave como entidad, la cual hace referencia a la ruptura longitudinal y transmural del esófago (previamente sano) secundaria a un aumento abrupto de la presión intraluminal esofágica, que se desencadena frecuentemente durante el vómito. Sin embargo, en la literatura médica existen algunos reportes que mencionan otros mecanismos de barotrauma diferentes a esta entidad. Reporte de caso: se presenta el caso de una paciente de 64 años con antecedente de adenocarcinoma gástrico manejado quirúrgicamente (gastrectomía total y anastomosis esofagoenteral), quien presentaba estenosis de anastomosis esofagoyeyunal, que requirió un protocolo de dilatación endoscópica con balón CRETM. Se llevó a una tercera sesión de dilatación endoscópica, en la que durante la extracción del endoscopio se identificó una laceración esofágica profunda con perforación de 4 cm de longitud a nivel del esófago medio (8 cm proximal a anastomosis dilatada), y se sospechó del mecanismo de barotrauma como agente causal. Requirió traslado urgente a sala de cirugía, en la que se realizó esofagorrafia por toracoscopia, cubrimiento antimicrobiano empírico de amplio espectro y nutrición enteral por sonda avanzada durante la vigilancia intrahospitalaria. El esofagograma de control a los 7 días mostró una pequeña fuga sobre el área anastomótica, la cual se manejó de manera conservadora. El control imagenológico a los 14 días evidenció una disminución del tamaño de la fuga, con una evolución satisfactoria y tolerancia a la vía oral, y posteriormente se dio el egreso.

Perforación esofágica espontánea

Resumen La perforación esofágica espontánea es una forma rara de ruptura del grosor de la pared del esófago sano, de manera no traumática. Es característico verla en pacientes de mediana edad, con obesidad y alcohólicos, que tienen episodios violentos de náuseas y vómitos. El tratamiento de la perforación esofágica espontánea depende de varios factores, como la etiología, sitio de la perforación, tiempo transcurrido desde la perforación hasta el diagnóstico, el grado de la contaminación del peritoneo o mediastino, comorbilidades, y estado general del paciente. En este artículo se presenta el caso de un paciente con enfisema subcutáneo en la parte superior del tórax, cuello y cara; con taquicardia de 115 latidos por minuto, hemograma con 18 mil leucocitos con predominio de neutrófilos. Se le realizaron radiografías de tórax y senos paranasales, donde se observa aire entre partes blandas y hueso. Se le realiza tratamiento quirúrgico con cierre de la perforación por toracotomía izquierda, se deja alimentación por sonda nasogástrica y antibióticos por 7 días.

Abstract Spontaneous esophageal perforation is a rare form of non-traumatic rupture of the thickness of the wall of the healthy esophagu. It is observed in middle-aged, obese, and alcoholic patients who have violent episodes of nausea and vomiting. Treatment of spontaneous esophageal perforation depends on several factors, such as the etiology, site of the perforation, time from perforation to diagnosis, degree of contamination of the peritoneum or mediastinum, comorbidities, and general condition of the patient. This article presents the case of a patient with subcutaneous emphysema in the upper part of the chest, neck and face; with a heart rate of 115 beats per minute, with a blood count of 18,000 leukocytes with a predominance of neutrophils. X-rays of the chest and paranasal sinuses were performed, where air is observed between soft tissue and bone. Surgical treatment is performed with closure of the perforation by left thoracotomy, feeding by nasogastric tube and antibiotics is left for 7 days.

Perforación esofágica espontánea: síndrome de Boerhaave. Caso clínico y revisión de la literatura / Boerhaave síndrome: spontaneous esophageal perforation. A clinical case and review of literature / Perfuração esofágica espontânea: síndrome de Boerhaave. Relato de caso e revisão bibliográfica

Resumen: La perforación esofágica espontánea o síndrome de Boerhaave es una entidad poco frecuente. Se define como la rotura del esófago no relacionada con traumatismos, exploraciones invasivas, patología esofágica previa o cuerpos extraños. Las roturas esofágicas se consideran como la perforación más grave del tracto digestivo, con una alta tasa de morbimortalidad relacionada principalmente con el desarrollo de mediastinitis posterior. Presentamos un paciente de sexo masculino de 63 años, que postingesta copiosa presenta esfuerzo de vómito inefectivo y posteriormente intenso dolor epigástrico, acompañado de enfisema subcutáneo. Se realiza tomografía de tórax que evidencia colección de contraste paraesofágica. Con planteo de síndrome de Boerhaave se decide cirugía de urgencia. Destacamos que el principal elemento pronóstico es el tiempo de resolución quirúrgica, por lo que debemos considerar esta patología como diagnóstico diferencial en pacientes con dolor torácico de inicio agudo.

Summary: Spontaneous esophageal perforation or Boerhaave syndrome is rather an unusual condition. It may be defined as the rupture of the esophagus that is not associated to trauma, invasive explorations, previous esophagus pathology or foreign bodies. Esophageal ruptures are considered as the most severe perforations of the digestive tract, with high morbimortality rates which are mainly associated to the development of subsequent mediastinitis. The study presents a 63-year-old patient who, after copious food intake, evidences unsuccessful effort to vomit effort and subsequent intense epigastric pain, accompanied by subcutaneous emphysema. Abdominal contrast scan reveals paraesophageal collection and a decision is made to perform an emergency surgery upon the suspicion of Boerhaave syndrome. It is worth pointing out that time for surgical resolution is the main prognostic element, and thus, this condition is to be considered as differential diagnosis in patients with acute thoracic pain.

Resumo: A perfuração esofágica espontânea ou síndrome de Boerhaave é uma entidade rara. É definida como ruptura do esôfago não relacionada a trauma, exames invasivos, patologia esofágica prévia ou corpos estranhos. As rupturas esofágicas são consideradas as perfurações mais graves do trato digestivo, com alto índice de morbimortalidade principalmente relacionado ao desenvolvimento de mediastinite posterior. Apresentamos um paciente do sexo masculino, 63 anos, que após ingestão abundante apresentou esforço ineficaz de vômito e, posteriormente, dor epigástrica intensa, acompanhada de enfisema subcutâneo. Foi realizada tomografia de tórax que evidenciou coleção de contraste paraesofágico. Com diagnóstico de síndrome de Boerhaave, a cirurgia de emergência foi decidida. Ressaltamos que o principal elemento prognóstico é o tempo de resolução cirúrgica, portanto, devemos considerar essa patologia como um diagnóstico diferencial em pacientes com dor torácica de início agudo.

Enfoque terapéutico en el Síndrome de Boerhaave / Therapeutic Approach of Boerhaave's Syndrome

RESUMEN Introducción: La perforación del esófago constituye una de las urgencias más graves y difíciles que ha de afrontar un cirujano por las características y ubicación del órgano. El pronóstico depende sobre todo de la rapidez del diagnóstico y de la elección del tratamiento instaurado en principio. Objetivo: Presentar un caso portador del Síndrome de Boerhaave. Caso clínico: Paciente masculino en la 5ta década de vida que acudió por dolor torácico posterior a cuadro emético. Luego de estudio radiográfico se diagnosticó ruptura espontánea de esófago o síndrome de Boerhaave. Conclusiones: El enfoque terapéutico adecuado asociado al diagnóstico oportuno y precoz del síndrome garantiza mejores índices de sobrevida(AU)

ABSTRACT Introduction: Esophageal perforation is one of the most serious and difficult emergencies that a surgeon has to face due to the characteristics and location of the organ. Such prognosis depends mainly on the speed of the diagnosis and the choice of treatment established initially. Objectives: To present a case with such syndrome and to review the literature to update the therapeutic approach of this entity given its high mortality. Clinical case: Male patient in the fifth decade of life who presented for chest pain after an emetic condition. After a radiographic study, a spontaneous rupture of the esophagus or Boerhaave syndrome was diagnosed. Conclusions: The appropriate therapeutic approach associated with the early and timely diagnosis of the syndrome guarantees better survival rates(AU)

Laparoscopic surgery by spontaneous rupture of the esophagus, a case report of treatment Boerhaave syndrome

Spontaneous rupture of the esophagus, Boerhaave syndrome, is a rare pathology and emergency condition for the patient. Patient, 63-year-old, on the 6th day of the disease falls into the clinic, where a Boerhaave syndrome was diagnosed. Laparoscopic surgery was performed. Sanitation and drainage of the mediastinum, suturing of the perforation hole were performed. After the operation, а positive response to treatment was observed. A group of authors believes that a minimally invasive approach to the treatment of spontaneous esophageal rupture is the alternative method for patients with severe somatic status and a small perforated opening of the esophagus.

Spontaneous Oesophageal Perforation: A Case Report

@#A 49-year-old gentleman presented with epigastric pain for one day associated with one episode of vomiting and dyspnoea. Respiratory examination showed reduced breath sound over his left lower zone. He was treated as left spontaneous pneumothorax and left lung empyema requiring left chest tube insertion and intravenous antibiotics. His left pleural fluid biochemistry result was exudative while its centrifuge showed empyema. In ward, we noticed food material draining from his left chest tube during feeding. An urgent contrast enhanced computed tomography (CECT) thorax showed a left oesophageal-pleural fistula with possible broncho-oesophageal fistula. During oesophagogastroduodenoscopy (OGDS), air bubbles were seen in his left under-water chest drainage during air-insufflation of the oesophagus. The revised diagnosis was Boerhaave syndrome. He was treated with an esophageal stent to cover the perforation and a left lung decortication via video assisted thoracoscopic surgery (VATS) for his left empyema. He improved and was discharged well.

Neumomediastino espontáneo: caso clínico y revisión de la literatura / Spontaneous pneumomediastinum: clinical case and review of the literature

El neumomediastino espontáneo es una entidad poco frecuente, caracterizada por la presencia de aire en el mediastino sin mediar antecedente traumático o iatrogénico. Fue descrito por primera vez en 1939 por Hamman, quien lo caracteriza como un síndrome que presenta dolor torácico y disnea, y cuya principal manifestación al examen físico es el enfisema subcutáneo. A continuación se presenta el caso clínico de un varón de 22 años con antecedentes de asma, tabaquismo activo y abuso de drogas, quien luego de consumir cocaína presenta un cuadro de 2 días de evolución de dolor cervical, al que posteriormente se le agrega disnea y sensación de opresión torácica, con enfisema subcutáneo al examen físico como único hallazgo. Se confirma el diagnóstico de neumomediastino espontáneo mediante radiografía de tórax posteroanterior (PA), y es hospitalizado por sospecha de mediastinitis la que posteriormente es descartada, evolucionando el paciente de forma favorable al cabo de 8 días de observación y tratamiento antibiótico preventivo. Se presenta el caso para revisar la incidencia de la patología, los factores de riesgo asociados, y principales diagnósticos diferenciales con el fin de mejorar la pesquisa en servicios de urgencia.

Spontaneous pneumomediastinum is an uncommon entity characterized by the presence of air in the mediastinum and not associated with trauma or iatrogenesis. It was first described by Hamman in 1939, who characterized it as a syndrome presenting with thoracic pain and dyspnea with subcutaneous emphysema on physical examination. We present the clinical case of a 22 year old asthmatic male who was an active smoker and drug abuser who, after using cocaine, suffered two days of neck pain then, in addition, dyspnea and thoracic oppression; subcutaneous emphysema being the only physical finding. Diagnosis was confirmed by an antero-posterior chest film, the patient was hospitalized with suspected mediastinitis, diagnosis which was subsequently discarded, and the patient responded favorably to 8 days observation and preventive antibiotics. We are presenting the case in order to review the incidence of this pathology, its risk factors and principal differential diagnoses in order to improve its detection rate in emergency services.

Successful Management of Delayed Esophageal Rupture with T-Tube Drainage Using Video-Assisted Thoracoscopic Surgery

Spontaneous perforation of the esophagus after forceful vomiting is known as Boerhaave syndrome, a rare and life-threatening condition associated with a high rate of mortality. The management of Boerhaave syndrome is challenging, especially when diagnosed late. Herein, we report the successful management of late-diagnosed Boerhaave syndrome with T-tube drainage in a 55-year-old man. The patient was transferred to our institution 8 days after the onset of symptoms, successfully managed by placing a T-tube, and was discharged on postoperative day 46 without complications.

Development of bilateral tension pneumothorax under anesthesia in a Boerhaave's syndrome patient: a case report / 대한마취과학회지

A 33-year-old male visited the emergency room with abdominal pain which developed after a vomiting episode. Based on the pneumomediastinum findings from a chest radiograph and a contrast-enhanced chest and abdominal computed tomography scan, the patient was diagnosed with Boerhaave's syndrome. Preoperative radiologic findings showed no pneumothorax or pleural effusion. Once anesthesia was administered, the patient developed near complete cardiopulmonary collapse due to a bilateral tension pneumothorax, which was treated by bilateral thoracentesis, followed by chest tube insertion. Despite a left side rupture, the damaged right lung was unable to overcome single right ventilation, so the surgery was completed via right thoracotomy. The ruptured site was treated, and the patient was transferred to the intensive care unit. We discuss the anesthetic implications of this disease and how to prevent fatal complications.

Clinical Analysis and Management of Esophageal Perforation / 대한이비인후과학회지

BACKGROUND AND OBJECTIVES: Esophageal perforation is relatively uncommon and requires careful diagnostic evaluation and expert management. It has a high mortality due to significant mediastinal and pleural contamination leading to sepsis and multiple organ failure. We reviewed our experience of esophageal perforation to determine how to better recognize such a lesion and facilitate its correct management. SUBJECTS AND METHOD: A retrospective chart review was performed on all patients treated for esophageal perforation from January 2000 to March 2016. These patients have been studied with respect to gender and age distribution, causes, sites, clinical manifestation, complications, management and postoperative complications. RESULTS: Patients ranged in age from 21 to 87 years, with an average age of 57.6±12.4 years. Fifty of the patients were men and 21 were women. The causes of the perforations were as follows: foreign body retention (18 patients), trauma (17 patients), Boerhaave's syndrome (22 patients), and iatrogenic (14 patients). The sites of esophageal perforation were: the cervical esophagus (25 patients), thoracic esophagus (44 patients) and abdominal esophagus (2 patients). Primary repair only was performed in seven (9.9%) patients, whereas 32 (45%) patients were treated with primary repair & patch, seven (9.9%) patients with T-tube drainage. Exclusion & division were performed in three (4.2%) patients and esophagectomy was performed in two (2.8%) patients. Twenty (28.2%) patients were treated conservatively. CONCLUSION: Early recognition and appropriate management of esophageal perforation are essential for reduction of morbidity and mortality.

Prótesis esofágica autoexpansible para tratamiento de síndrome de Boerhaave: a propósito de un caso / Self-expanding esophageal stent for treatment of Boerhaave syndrome: report of a case

La perforación esofágica espontánea (PEE) o síndrome de Boerhaave es una entidad poco frecuente, consiste en la ruptura del esófago no relacionada con traumatismos, exploraciones invasivas, patología esofágica previa o cuerpos extraños. Independientemente de su mecanismo de producción, la perforación esofágica se considera como la más grave del tracto digestivo. Si su diagnóstico y reparación quirúrgica se retrasan, el pronóstico se ensombrece de forma notable. Presentamos un caso de paciente masculino de 37 años, sin antecedentes de interés que consulta a emergencia por cuadro brusco de dolor epigástrico irradiado a región retroesternal, posterior a vómito de contenido alimentario. El paciente presenta progresivamente deterioro de sus condiciones ventilatorias, que ameritan traslado a UCI y 72 horas posterior a ingreso a UCI se realizó esofagograma con bario evidenciándose extravasación de medio de contraste en tercio distal esofágico, aproximadamente 3 cm por encima de hemidiafragma izquierdo, por lo que de inmediato se decide colocación de stent metálico parcialmente cubierto Wilson-Cook (Evolution) bajo visión endoscópica y fluoroscópica, con resolución completa de la sintomatología

Spontaneous esophageal perforation (SEP) or Boerhaave syndrome is a rare entity that consists in the rupture of the esophagus unrelated to trauma, invasive examinations, previous esophageal disease or the presence of foreign bodies. Regardless of its mechanism, esophageal perforation is considered the most serious of the digestive tract. If diagnosis and surgical repair are delayed the outlook worsens considerably. We present the case of a 37-year-old male patient in good health, who attends the emergency room because of sudden onset of epigastric pain radiating to the retrosternal region after vomiting. The patient´s ventilatory condition deteriorated progressively meriting transfer to the intensive care unit; 72 hours after admission, a barium esophagram showed dye extravasation in the distal esophagus, approx 3 cm above the left diaphragm. We immediately decided to place a Wilson-Cook partially covered metal stent (Evolution) through endoscopic and fluoroscopic guidance with complete resolution of symptoms

Boerhaave's syndrome: a differential diagnosis of acute chest pain following a vomiting illness / Síndrome de Boerhaave: un diagnóstico diferencial de dolor torácico, agudo tras enfermedad acompañada de vómitos

Spontaneous oesophageal rupture (Boerhaave's syndrome) is extremely rare in children. Presentation is usually in middle aged men as a result of vomiting following heavy food or alcohol consumption. We describe an unusual case of a 12-year old boy without significant past medical history presenting with acute chest pain following gastroenteritis.

La ruptura esofágica espontánea (síndrome de Boerhaave) es extremadamente rara en niños. Por lo general se presenta en hombres de mediana edad como resultado vómitos tras la ingestión de alcohol o alimentos pesados. Describimos un caso inusual de un niño de 12 años de edad sin antecedentes clínicos significativos, que acudió con dolor torácico agudo tras una gastroenteritis.

Boerhaave Syndrome Presenting as Abrupt Onset of Massive Hydropneumothorax

Boerhaave syndrome is a rare and life-threatening disease that often presents a diagnostic challenge. It is usually confused with critical but more prevalent diseases such as acute myocardial infarction, perforated peptic ulcer, and acute pancreatitis. Boerhaave syndrome is caused by forceful vomiting resulting in a full-thickness tear of the middle or lower esophagus, typically an area of natural narrowing and at the esophagogastric junction and the left atrium. Because of these anatomic sites, hydropneumothorax, hemopneumothorax and pneumopericardium can occur. We report a case of a 48-year-old chronic alcoholic man presenting with abrupt onset of massive bilateral hydropneumothorax. In this case, it was hard to take a medical history from the patient due to sudden respiratory arrest when he arrived at the emergency room. Despite ongoing chest tube drainage, hydropneumothorax didn't improve. Pleural fluid amylase level was increased. Because of the possibility of esophageal rupture, esophagography was performed. As a result of the esophagography, he was diagnosed as Boerhaave syndrome with penumopericardium. If massive hydropneumothorax of unknown cause presents abruptly, boerhaave syndrome should be suspected as one of its causes. We recommend that pleural fluid amylase levels to be checked and if it is elevated, esophagography should be performed immediately.

Two Cases of Boerhaave's Syndrome Treated by Endoscopic Hemoclipping / 대한소화기내시경학회지

Boerhaave's syndrome is a spontaneous esophageal perforation due to severe nausea and vomiting after hyperphagia or drinking, and it is not due to trauma, medical instrumentation or a foreign body. Untreated esophageal perforation is associated with high mortality, and the traditional treatment has been surgical drainage and primary repair of the perforation. However, non-surgical primary repair with an endoscopic procedure has recently been attempted in some selected patients with a small sized perforation, limited contamination of the mediastinum and no evidence of sepsis. We report here on 2 patients with Boerhaave's syndrome and who were successfully treated via primary repair with endoscopic hemoclips, and we review the other cases of the Boerhaave's syndrome that were treated with a endoscopic procedure.

Síndrome de Boerhaave: Reporte de un caso y revisión de la literatura

El síndrome de Boerhaave o perforación esofágica espontánea es una enfermedad grave que pone en riesgo la vida y amerita un diagnóstico oportuno. Sin tratamiento médico o quirúrgico es prácticamente letal. El cuadro clásico es el del paciente que presenta vómito y posteriormente dolor epigástrico o retroesternal. Caso Clínico: se rata de peciente femenina de 23 años de edad quien consulto por presentar Posterior a ingesta de alimentos sensación de deglución incompleta, vómitos de contenido Hematico y dolor retroesternal. Se realiza Gastroscopia evidenciándose en esófago a 25 cm. laceración lineal profunda que se extiende hasta los 33cm TAC de tórax reporto: Neumonediastino, Signos sugestivos de perforación esofágica; Se realizo Toracotomia Posterolateral derecha, encantándose 50cc de liquido libre en cavidad, hematoma mediastinal de 4 x 4 cm y enfisema mediastinal. La paciente permaneció hospitalizada por varios días recibiendo tratamiento medico evolucionando satisfactoriamente sin complicaciones. Conclusiones: el diagnóstico y tratamiento precoces del SB es muy importantes ya que permiten reducir las altas tasas de morbilidad y mortalidad asociadas a este cuadro. Sin embargo, el diagnóstico de esta entidad muestra en general retraso en prácticamente todas las series (en la mitad de los casos el diagnóstico se realiza con más de 24 horas de evolución), ya que en muchas ocasiones los síntomas son inespecíficos y no típicos, además los hallazgos clínicos y radiológicos pueden no ser aparentes en las primeras horas tras la perforación. Estudios de Endoscopia, esofagograma, TAC proporcionan el diagnóstico.

Boerhaave syndrome or spontaneous esophageal perforation is a serious condition that endangers the patient´s life and deserves an opportune diagnosis. Without medical or surgical treatment is practically lethal. The classic presentation is the patient who presents with vomits and immediately after with epigastric or retrosternal pain. Clinical case: a 23 years old female patient consulted presenting, after food ingestion, a subsequent sensation of incomplete swallowing, vomits with hematic content and retrosternal pain. A gastroscopy was performed demonstrating deep linear esophagial laceration at 25 cm extending at 33cm CT scan reported pneumonediastin, with suggestive signs of esophageal perforation; She went through a right posterolateral toracotomy, 50cc of free liquid was found in cavity, a 4 x 4 cms mediastinal hematoma and emphysema. The patient remained hospitalized for several days receiving medical treatment without complications. Conclusions: early diagnosis and treatment of BS is important becuase it reduces the high morbidity and mortality rates associated with this syndrome. Nevertheless, the diagnosis is usually delayed in practically all series (in half of the cases the diagnosis is done after more than 24 hours), since in many occasions the symptoms are inespecífic and non-typical. in addition the clinical and radiological findings are not apparent in the first hours after perforation. Studies as endoscopy, esophagogram, CT scan provide the diagnosis.

Non-surgical Treatment with Endoscopic Clipping in a Patient with Boerhaave's Syndrome / 대한소화기내시경학회지

Boerhaave's syndrome is difficult to diagnosis because of the esophageal rupture, which is caused by nausea and vomiting, and Boerhaave's syndrome is known to have a high mortality rate. The mortality increases with a delayed diagnosis; therefore, an early diagnosis and surgical treatment are critical for a good prognosis. Yet some recent cases have shown that non-surgical treatments are successful in some classified patient groups. These groups should be considered according to their symptoms and their laboratory and radiological findings. Sepsis and multi-organ failure should be continuously checked for to see if they occurred and/or progressed. We report here on a 51 year old woman who had Boerhaave's syndrome, and this was caused by heavy drinking, nausea and vomiting, and she improved with just non-surgical treatment such as fasting, antibiotics and endoscopic clipping.

Spontaneous Pharyngeal Perforation After Forceful Vomiting: The Difference from Classic Boerhaave's Syndrome

Boerhaave's syndrome is spontaneous transmural perforation of the esophagus, which occurs most often after forceful vomiting or retching. This commonly occurs in the lower third of the esophagus but spontaneous perforation of the pharynx or cervical esophagus is extremely rare. This case presented a 20-yr-old healthy man with spontaneous pharyngeal perforation after forceful vomiting who had no history of instrumentation, cervical trauma, or having eaten anything sharp. Cervical pain and crepitus were the early symptom and sign of pharyngeal perforation and the rupture was detected on gastrografin swallow and CT examinations. The rupture site was higher than the upper esophageal sphincter, differing from Boerhaave's syndrome. The patient was conservatively managed without significant morbidity and mortality. Although this may resolve without surgical intervention, the pharyngeal rupture should receive early detection and clinical attention for preventing potential morbidity by late diagnosis.

A Case of Nonsurgical Treatment in Boerhaave's Syndorme during Diagnostic Endoscopy / 대한소화기내시경학회지

Boerhaave's syndrome is a rare spontaneous rupture of the esophagus that requires an immediate diagnosis and surgical repair. It might result from a severe and uncoordinated contraction of the esophagus and stomach. The rate of mortality and morbidity can increase with increasing time between the onset and treatment. In recent years, there have been some reports of non-surgical treatment in cases with perforation but with minimal symptoms and clinical evidence of the systemic effects such as sepsis. We experienced a case of Boerhaave's syndrome occurring during an endoscopic examination that was treated successfully using non-surgical measures.