Repair of complex esophageal atresia with tracheobronchial remnant using special magnets [0.03%]
应用特殊磁铁修复带有支气管残迹的复杂食道闭锁
Charlotte Reich,Elena Weigl,Anne-Sophie Holler et al.
Charlotte Reich et al.
Esophageal atresia (EA) repair can be complicated by associated malformations such as a tracheobronchial remnant in the distal esophagus. We describe our experience with a patient found to have long-gap EA with a distal cartilaginous ring w...
Colonic Resection in an 8-Year-Old Girl with Intractable Functional Constipation and Diffuse Colonic Dysmotility and Failed Antegrade Flushes [0.03%]
一名8岁女孩出现难治性功能性便秘和弥漫性结肠运动障碍，并且逆行冲水失败后的结肠切除术
Gabriella Danziger,Thomas O Xu,Teresa Lynn Russell et al.
Gabriella Danziger et al.
Optimal surgical management of patients with intractable constipation and diffuse colonic motility is not well defined. We present a patient with such a history, who ultimately achieved successful surgical management of constipation through...
Unintentional Suture Fistula Between the Proximal and Distal Esophagus in a Preterm Neonate with Type C Esophageal Atresia [0.03%]
C型食管闭锁早产儿近端和远端食管之间非意图的缝合窦道
Julia E Menso,Maud A Reijntjes,Carlijn M Mussies et al.
Julia E Menso et al.
We present the case of a patient with gross type C esophageal atresia in a preterm neonate (gestational age of 31 weeks + 1 day) with a birth weight of 1,470 g. The fistula was released via a thoracotomy, but no primary anastomosis could be...
Neonatal Sacrococcygeal Fetiform Teratoma Containing Bowel: A Case Report [0.03%]
含有肠的新生儿骶尾部胎儿型畸胎瘤一例报告
Ashley Toms,Tarlia Rasa Govender,Giulia Brisighelli et al.
Ashley Toms et al.
A fetiform sacrococcygeal teratoma (homunculus) is a highly differentiated subgroup of mature cystic teratoma that resembles a malformed fetus. These tumors originate at the base of the coccyx and may vary in their intrapelvic and extrapelv...
Ureteroinguinal Herniation with Consecutive Ureteral Stricture in a 2-Month-Old Infant: Case Report [0.03%]
两个月大婴儿发生尿肠疝并继发尿道狭窄一例报告
Carlos Delgado-Miguel,Antonio Jesus Muñoz-Serrano,Pablo Aguado et al.
Carlos Delgado-Miguel et al.
Inguinal herniation of ureter is an uncommon finding among children, with scarce reported cases in the literature to date, that can potentially lead to obstructive uropathy. We report a case of ureteroinguinal herniation discovered during a...
Tobias Krause,Dietmar Cholewa,Benjamin Liniger et al.
Tobias Krause et al.
Accessory liver lobes are rare. We present the rare case of torsion of an accessory liver lobe in a neonate. A 13-day-old newborn presented with failure to thrive and hematemesis without fever. The initial workup with sonography, magnetic r...
Missed Proximal Tracheoesophageal Fistula (TEF) in a Neonate with Type D Esophageal Atresia [0.03%]
错失诊断的D型食管闭锁新生儿合并 proximal 气管食管瘘（TEF）
Julia E Menso,Maud A Reijntjes,Matthijs W Oomen et al.
Julia E Menso et al.
We present the case of a patient with the rare type D esophageal atresia (EA), diagnosed after correction of an EA initially diagnosed as type C. Routine postoperative contrast esophagogram showed a missed proximal tracheoesophageal fistula...
Massive Chylous Ascites in a 9-Year-Old Girl with Malrotation-A Case Report [0.03%]
一名患有畸形的九岁小女孩出现大量乳糜腹水 – 一个病例研究
Hans Winberg,Pär Gerwins,Kristine Hagelsteen
Hans Winberg
Malrotation leading to massive chylous ascites is rare. A 9-year-old girl was investigated for slowly increasing abdominal distension under a year. She had no vomiting, weight loss, or pain, but was bothered in social situations. Medical in...
Congenital Internal Jugular Phlebectasia: An Anomaly Still Poorly Recognized [0.03%]
先天性颈内静脉曲张：一种仍未被充分认识的异常现象
Alessandro Raffaele,Marta Gazzaneo,Piero Romano et al.
Alessandro Raffaele et al.
Congenital internal jugular phlebectasia (CIJP) is a rare condition characterized by congenital dilatation of the vein without tortuosity that becomes more evident during straining as a lateral neck mass. CIJP often remains undiagnosed from...
Combined Pre- and Postnatal Minimally Invasive Approach to a Complex Symptomatic Congenital Pulmonary Airway Malformation [0.03%]
复杂症状性先天性支气管肺隔离症的产前和产后微创治疗联合策略
Francesco Macchini,Stefano Mazzoleni,Giacomo Cavallaro et al.
Francesco Macchini et al.
Congenital pulmonary airway malformation (CPAM) is a rare congenital lung lesion that usually remains asymptomatic during the fetal and neonatal period. However, it can occasionally cause prenatal cardiocirculatory failure and fetal hydrops...