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1.
J Cardiothorac Surg ; 18(1): 238, 2023 Jul 26.
Article in English | MEDLINE | ID: mdl-37496023

ABSTRACT

BACKGROUND: Esophageal duplication cysts are rare congenital tumors usually diagnosed and treated during childhood. Most of them are located in the mediastinum and appear as a mass besides the esophagus. Unfortunately, symptoms are non-specific and depend on the size and location of the mass; therefore, they can easily be missed. If symptoms appear, surgical resection is necessary to prevent troublesome complications. CASE PRESENTATION: We present the case of a 60-year-old woman who presented with severe progressive dysphagia and epigastric pain. After further evaluation, a paraesophageal cystic mass was found, and surgery was required. Non-communicating esophageal duplication cyst was the final diagnosis. CONCLUSION: Esophageal duplication cysts are a rare pathology in adults; their symptoms will vary depending on their size and location. Preoperative diagnosis is difficult as symptoms are non-specific and can be missed. If severe dysphagia, pain, or any other complication appears, surgery should not be delayed.


Subject(s)
Deglutition Disorders , Esophageal Cyst , Adult , Female , Humans , Middle Aged , Deglutition Disorders/etiology , Esophageal Cyst/complications , Esophageal Cyst/diagnosis , Esophageal Cyst/surgery , Esophagoscopy , Pain
4.
Medicine (Baltimore) ; 98(28): e16364, 2019 Jul.
Article in English | MEDLINE | ID: mdl-31305433

ABSTRACT

RATIONALE: Esophageal duplication cyst (EDC) is a rare developmental aberration originated from the embryonic foregut. It may remain asymptomatic but produce local mass effect on surrounding organs if rapid enlarges. EDC may sometimes accompany with other congenital malformations. Congenital pulmonary airway malformation (CPAM) is a congenital lung malformation with an unknown chance of developing symptoms. Here we report a rare case of esophageal duplication cyst with type 2 congenital pulmonary airway malformation (CPAM). PATIENT CONCERNS: A 16-month old boy with a prenatal diagnosis of type 2 CPAM presented progressive stridor and respiratory distress and was admitted to our hospital under the diagnosis of pneumonia. The patient responded poorly to antibiotics. A chest Xray (CXR) showed consolidation over the left upper lobe with trachea deviated to right side. A chest computed tomography (CT) revealed a cystic lesion sized 3.3 × 3.3 cm in the superior mediastinum. DIAGNOSES: Post-operative pathological report confirmed the diagnosis of esophageal duplication cyst. INTERVENTIONS: We pre-medicated the patient with steroids and inhaled bronchodilators for airway maintenance. Then the patient received tumor resection via median sternotomy. OUTCOMES: The patient recovered without complication and discharged smoothly 4 days after the surgery. LESSONS: EDC is a rare but potentially life-threatening disease owning to compression of large airways. Chest CT scan could detect the lesion non-invasively and should be considered in patients with persistent stridor, as well as CXR findings of the trachea deviated by a mass lesion in mediastinum, especially for those with CPAM.


Subject(s)
Congenital Abnormalities , Esophageal Cyst/complications , Esophagus/abnormalities , Larynx/abnormalities , Lung/abnormalities , Respiratory Sounds , Congenital Abnormalities/diagnosis , Congenital Abnormalities/therapy , Diagnosis, Differential , Esophageal Cyst/diagnosis , Esophageal Cyst/therapy , Esophagus/diagnostic imaging , Esophagus/surgery , Humans , Infant , Lung/diagnostic imaging , Male , Respiratory Sounds/diagnosis
8.
Medicine (Baltimore) ; 94(49): e2270, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26656375

ABSTRACT

Esophageal duplication cysts (EDCs) are rare developmental anomalies. They may occur anywhere along the esophagus with the predominant location in the thoracic segment. Presently, most are diagnosed prenatally or in early childhood. The prevalence of EDCs is estimated at 1 in 8200 live births. Usually, cysts are asymptomatic in the neonatal period, but they may cause respiratory distress or feeding difficulties depending on the size and location of the lesion.This report presents a female neonate with a cyst located in the right pleural cavity recognized prenatally. Computed tomography confirmed the diagnosis and revealed a round cystic mass in proximity to the left lung base. Thoracoscopic cyst excision was undertaken on day 15 after delivery. The postoperative period was uneventful. Histological cyst examination confirmed the diagnosis of foregut duplication.This case underlines the importance of early diagnosis and treatment of EDC, before symptoms and complications arise, and confirms that surgery in the neonatal period is safe and effective.


Subject(s)
Esophageal Cyst/diagnosis , Esophageal Cyst/surgery , Thoracoscopy/methods , Ultrasonography, Prenatal/methods , Female , Gestational Age , Humans , Infant, Newborn
9.
Ann Ital Chir ; 86(ePub)2015 Jun 15.
Article in English | MEDLINE | ID: mdl-26098121

ABSTRACT

AIM: Bronchogenic cysts are congenital lesions deriving from the primitive foregut, and are usually located in close relation to tracheobronchial tree or oesophagus. We report a case of an oesophageal bronchogenic cyst appearing at preoperative examinations as a benign fibromuscular tumour (leiomyoma). CASE REPORT: A 62 years old male patient in good general conditions, was admitted to our Institution because of moderate dysphagia and upper post-prandial abdominal pain. Conventional imaging, endoscopy and echo endoscopy detected a parietal oesophageal wall mass looking like a solid formation, determining extrinsic compression and narrowing of the lumen. RESULTS: The mass has been radically removed with thoracoscopic approach. Postoperative stay was uneventful and the patient was discharged three days after the operation. At histological examination the mass appeared as a cystic formation with fibromuscular wall and ciliated epithelium (so-called disembriogenetic bronchogenic cyst). CONCLUSION: The case we have reported describes a very unusual case of a voluminous symptomatic intramural oesophageal disembriogenetic cyst whose characteristics had not been defined at preoperative examinations. Surgical removal of the mass has been achieved with a minimally invasive approach.


Subject(s)
Bronchogenic Cyst/surgery , Esophageal Cyst/surgery , Thoracoscopy/methods , Abdominal Pain/etiology , Bronchogenic Cyst/diagnosis , Bronchogenic Cyst/embryology , Bronchogenic Cyst/pathology , Deglutition Disorders/etiology , Diagnosis, Differential , Esophageal Cyst/diagnosis , Esophageal Cyst/embryology , Esophageal Cyst/pathology , Humans , Leiomyoma/diagnosis , Male , Middle Aged , Minimally Invasive Surgical Procedures
10.
Pediatr Surg Int ; 31(7): 683-7, 2015 Jul.
Article in English | MEDLINE | ID: mdl-26002606

ABSTRACT

Bronchogenic cysts are congenital cystic lesions of foregut origin, usually intrapulmonary or mediastinal, while esophageal cysts generally originate within the esophagus. To the best of our knowledge, this is the first report of a case of a completely intramural bronchogenic cyst of the cervical esophagus in a neonate.


Subject(s)
Bronchogenic Cyst/surgery , Esophageal Cyst/surgery , Bronchogenic Cyst/diagnosis , Esophageal Cyst/diagnosis , Esophagus/pathology , Esophagus/surgery , Humans , Infant, Newborn , Magnetic Resonance Imaging , Male
11.
Eur Arch Otorhinolaryngol ; 272(6): 1543-6, 2015 Jun.
Article in English | MEDLINE | ID: mdl-25543306

ABSTRACT

Oesophageal duplication cysts are a rare congenital anomaly of the foregut which usually present in infancy with respiratory symptoms, recurrent pneumonia and feeding difficulty. Other presenting symptoms depend on the location of the cyst and can include dysphagia, chest pain, arrhythmias and features of mediastinal compression. Treatment is usually surgical resection, recommended for complete resolution of symptoms, histological diagnosis and exclusion of malignancy. Here, we present a case of infected oesophageal duplication cyst which presents as a neck lump in a 43-year-old female with a background of Goltz syndrome, azygos fissure and congenital aortic stenosis. Surgical resection was decided against owing to the patient's high risk secondary to co-morbidities and instead ultrasound guided drainage was carried out successfully. The patient was symptom free and well at 1-year follow-up. Oesophageal duplication is an unusual presentation of a neck lump in an adult and whilst the usual treatment is surgical resection, we present here a case treated in an entirely different manner.


Subject(s)
Abnormalities, Multiple , Aortic Valve Stenosis/congenital , Azygos Vein/abnormalities , Drainage/methods , Esophageal Cyst , Focal Dermal Hypoplasia/diagnosis , Neck Dissection/methods , Adult , Anti-Bacterial Agents/administration & dosage , Diagnosis, Differential , Esophageal Cyst/complications , Esophageal Cyst/congenital , Esophageal Cyst/diagnosis , Esophageal Cyst/physiopathology , Esophageal Cyst/surgery , Female , Humans , Tomography, X-Ray Computed , Treatment Outcome , Ultrasonography, Interventional/methods
12.
Asian Cardiovasc Thorac Ann ; 23(3): 332-4, 2015 Mar.
Article in English | MEDLINE | ID: mdl-24757179

ABSTRACT

Esophageal duplication cyst is a rare congenital mediastinal cyst. Most of these cysts become symptomatic in childhood and only rare cases remain asymptomatic until adolescence. They may produce symptoms due to esophageal and respiratory system compression, rupture, and infection. A 25-year-old man presented with pulmonary infection and bronchiectasis that did not improve with medical treatment. A diagnosis of esophageal duplication cyst was made intraoperatively.


Subject(s)
Bronchiectasis/etiology , Esophageal Cyst/diagnosis , Esophagus/abnormalities , Pulmonary Infarction/etiology , Rare Diseases/diagnosis , Thoracotomy , Adult , Anti-Infective Agents/therapeutic use , Bronchiectasis/drug therapy , Diagnosis, Differential , Esophageal Cyst/complications , Esophageal Cyst/surgery , Esophagus/surgery , Humans , Male , Pulmonary Infarction/drug therapy , Rare Diseases/complications , Rare Diseases/surgery , Treatment Failure
15.
Pediatr Emerg Care ; 30(11): 812-3, 2014 Nov.
Article in English | MEDLINE | ID: mdl-25373566

ABSTRACT

Chest pain in children is commonly caused by benign etiologies but may be caused by conditions that carry significant morbidity if not treated. Emergency medicine physicians must identify the patients that require further evaluation and treatment. We describe a case of a 13-year-old boy with 10 months of progressive chest pain that had been attributed to anxiety and was ultimately diagnosed as an esophageal duplication cyst requiring surgical repair.


Subject(s)
Esophageal Cyst/diagnosis , Esophagus/abnormalities , Adolescent , Anxiety/etiology , Chest Pain/etiology , Esophageal Cyst/complications , Humans , Male
18.
J Cardiothorac Surg ; 8: 221, 2013 Dec 01.
Article in English | MEDLINE | ID: mdl-24289795

ABSTRACT

Esophageal duplication cyst (EDC) is a congenital malformation of the posterior primitive foregut, which mainly occurs in the thoracic esophagus. Here, we describe a 3-year-old Han Chinese boy afflicted with intermittent fever of acute onset and dry cough. Thoracic computed tomography revealed an 10 cm × 5.4 cm × 5.8 cm oval-shaped, cyst-like tumor located in the extrapleural space, extending along the right paravertebral gutter and compressing the trachea forward. An additional small-sized, oval-shaped cyst was identified in the posterior mediastinum, between the esophagus and the spinal column, at the T1 level. During open thoracotomy, under general anesthesia, an opaque, thick-walled, esophageal cyst was revealed not to be in communication with the esophageal lumen or the trachea. This cyst was subsequently resected in an en bloc manner. The small (1-cm) esophageal cyst was left untreated based on a "wait-and-see" policy. Histological analysis showed that the resected cyst was walled by hyperplastic, fibrous tissues and locally lined with gastric mucosa inherent glands. This finding was consistent with a diagnosis of EDC, with ectopic gastric mucosa. The respiratory tract symptoms resolved immediately after the operation. Computed tomography obtained at the 6-month follow-up showed that no disease, residual or recurrence, was present after the resection of the large-sized cyst, and the small-sized cyst remained unchanged in size.


Subject(s)
Esophageal Cyst/diagnosis , Gastric Mucosa/pathology , Mediastinal Cyst/diagnosis , Child, Preschool , Esophageal Cyst/congenital , Esophageal Cyst/pathology , Esophageal Cyst/surgery , Humans , Male , Mediastinal Cyst/congenital , Mediastinal Cyst/pathology , Mediastinal Cyst/surgery , Thoracotomy , Tomography, X-Ray Computed
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