Issam Saliba,Nazir El Khatib,Antoine Nehme et al.
Issam Saliba et al.
Myoepithelial carcinoma is a rare malignancy of the parotid gland that is usually seen in adults. We report the first case in children of myoepithelial carcinoma of the parotid gland with massive invasion of the facial nerve and metastasis ...
Internet impact on the insertion of genitourinary tract foreign bodies in childhood [0.03%]
互联网对儿童泌尿生殖道异物插入的影响
Xenophon Sinopidis,Vasileios Alexopoulos,Antonios Panagidis et al.
Xenophon Sinopidis et al.
Foreign body self-insertion into the urethra is an uncommon paraphilia. Variety in object form, motivation, clinical presentation, complications, and treatment options is a rule. In childhood it is very rare, and it is attributed to curiosi...
Matteo Chiappedi,Anna Fresca,Ilaria Maria Carlotta Baschenis
Matteo Chiappedi
Corpus callosum agenesis is a relatively common brain malformation. It can be isolated or included in a complex alteration of brain (or sometimes even whole body) morphology. Etiology and pathogenetic mechanisms have been better understood ...
Infantile myofibroma eroding into the frontal bone: a case report and review of its histopathologic differential diagnosis [0.03%]
婴幼儿肌纤维瘤侵入额骨：1例报告和病理鉴别诊断文献复习
Aatish Thennavan,Venkadasalapathi Narayanaswamy,Thanvir Mohammed Niazi et al.
Aatish Thennavan et al.
Infantile myofibroma is a rare and benign tumour of children presenting in the head and neck region. Rendering a final diagnosis of infantile myofibroma can be challenging in the light of nonspecific clinical, radiological findings and its ...
Endolymphatic sac enlargement in a girl with a novel mutation for distal renal tubular acidosis and severe deafness [0.03%]
一例远端肾小管性酸中毒和重度耳聋新型突变患者的内淋巴囊扩大症报告
Rink Nikki,Bitzan Martin,O&#x;Gorman Gus et al.
Rink Nikki et al.
Hereditary distal renal tubular acidosis (dRTA) is caused by mutations of genes encoding subunits of the H(+)-ATPase (ATP6V0A4 and ATP6V1B1) expressed in α-intercalated cells of the distal renal tubule and in the cochlea. We report on a 2-...
ECMO for Cardiac Rescue after Accidental Intravenous Mepivacaine Application [0.03%]
误静脉注射卡因丁后使用叶克膜急救成功个案报告
Michael Froehle,Nikolaus A Haas,Guenther Kirchner et al.
Michael Froehle et al.
Mepivacaine is a potent local anaesthetic and used for infiltration and regional anaesthesia in adults and pediatric patients. Intoxications with mepivacaine affect mainly the CNS and the cardiovascular system. We present a case of accident...
Severe gastrooesophageal reflux disease associated with foetal alcohol syndrome [0.03%]
与胎儿酒精综合症相关的严重胃食管反流病
N K Sujay,Matthew Jones,Emma Whittle et al.
N K Sujay et al.
Prenatal alcohol exposure may have adverse effects on the developing foetus resulting in significant growth restriction, characteristic craniofacial features, and central nervous system dysfunction. The toxic effects of alcohol on the devel...
Jolly Chandran,Rimi Manners,Indira Agarwal et al.
Jolly Chandran et al.
Hair dye ingestion with suicidal intention has increased among rural Indian population and is associated with significant mortality. We report a teenager who presented with cervicofacial edema, respiratory distress, rhabdomyolysis, and myoc...
Pulmonary alveolar proteinosis in association with congenital dyserythropoietic anemia: a case report [0.03%]
与先天性红细胞生成异常性贫血相关的肺泡蛋白沉积症1例报告
Marcus A Carden,Ashish Barman,Gita Massey
Marcus A Carden
A two-year-old girl with congenital dyserythropoietic anemia (CDA) acutely developed fever, tachypnea, and increased oxygen requirement. Chest X-ray revealed bilateral interstitial infiltrates and mild cardiomegaly. Blood cultures grew no i...
Case Reports
Case reports in pediatrics. 2012:2012:624740. DOI:10.1155/2012/624740 2012
Mild form of treacher collins syndrome imitating juvenile otosclerosis [0.03%]
轻型Treacher Collins综合征误诊为青少年otosclerosis
Karol Zeleník,Pavel Komínek
Karol Zeleník
Treacher Collins syndrome (TCS) is an inherited developmental disorder. More than 40% of individuals with TCS have conductive hearing loss attributed to external and middle ear anomalies. Mild cases of TCS often pass undiagnosed at birth or...