A case of cervical esophageal duplication cyst in a newborn infant
نویسندگان
چکیده
منابع مشابه
A case of cervical esophageal duplication cyst in a newborn infant
Esophageal duplication cyst is a rare congenital anomaly resulting from a foregut budding error during the fourth to sixth week of embryonic development. Cervical esophageal duplication cysts are very rare and may cause respiratory distress in infancy. A full-term newborn girl who was born by normal delivery was transferred to our hospital because of swelling of the right anterior neck since bi...
متن کاملA cervicothoracic esophageal duplication cyst in an infant and review of literature
Cervical esophageal duplication cysts are uncommon congenital malformations, and those with air-fluid level are rarely reported. We describe here a case of cervicothoracic esophageal duplication cyst manifesting air-fluid level on Computed Tomography (CT) in a 6-month-old girl. The preoperative diagnosis was suspected as esophageal duplication or abscess. The postoperative pathological diagnosi...
متن کاملCombined esophageal duplication cyst with bronchogenic cyst.
Ultrasonogram revealed cystic lesion in the right upper chest with internal echoes. Barium swallow showed a mass lesion causing smooth indentation of the esophageal outline (Fig. 1). At surgery, a cyst was identified in the posterior mediastinum, which was para-esophageal in location extending into the superior mediastinum. After excision, clinical improvement was rapid and child is well 8 mont...
متن کاملA Distal Urethral Cyst in a Female Newborn (A Rare Case)
Skene's glands are the largest external secretory glands in the distal part of the urethra. Although cystic changes caused by abnormal accumulation of significant amounts of secretions are rare, they can be seen even at birth. The presented case was a female full-term newborn with vaginal delivery. This was the second pregnancy of her mother after another living child. The mother was 26 years o...
متن کاملEsophageal duplication cyst with hemivertebrae
BACKGROUND Esophageal duplication cysts (EDCs) are rare congenital anomalies that can be associated with symptomatic spinal abnormalities, but presentations due to EDC symptoms are rarely found in the presence of spinal abnormalities. CASE SUMMARY A 6-month-old infant weighing approximately 5.0 kg presented with a 2-month pulmonary infection and more recent difficulty swallowing and nutrition...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Surgical Case Reports
سال: 2016
ISSN: 2198-7793
DOI: 10.1186/s40792-016-0157-2