Most of these injuries are preventable in infancy and childhood by ensuring proper vigilance, tender care by the parents and the caretakers. Safe driving techniques have to be followed by parents while traveling with children in their motor vehicles. Need to focus on grading the severity of TBI rather than on factors like age, mode of injury, and presence or absence of external injuries.
Background: With worldwide presence, Novel influenza virus (H1N1) carries great potential for causing a pandemic,there are limited studies about clinical profile of H1N1 in paediatric age group in India hence the present study was undertaken at Aditya Birla Memorial Hospital in Pune.
Pleuropulmonary blastoma (PPB) is a very rare, highly aggressive, and malignant tumor that originates from either lungs or pleura. It occurs mainly in children aged <5 or 6 years. It has poor prognosis with three different subtypes: cystic (type I), combined cystic and solid (type II), and solid (type III). PPB is treated with aggressive multimodal therapies including surgery and chemotherapy. We present a case of PPB in a 3-year-old girl who presented with tension pneumothorax.
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BSTRACT
Aneurysm in the extracranial segment of the internal carotid artery is extremely rare in children. Traumatic aneurysms of the internal carotid artery are generally “false aneurysms” (pseudoaneurysms) with at least part of the aneurysm wall composed only of the adventitial layer, or even just by the hematoma. There are few reports in the world medical literature about its etiology, presenting features, and catastrophic consequences. The natural history of the disease has not been well-defined yet. However, the potential risk of embolism originating from the aneurysm or even its rupture indicates a need for early diagnosis and intervention. We present a 12-year-old previously healthy child with recurrent oropharyngeal hemorrhage leading to massive hematemesis and hypovolemic shock due to right-sided internal carotid artery pseudoaneurysm with hemorrhage and right middle cerebral artery territory infarct. The child required urgent endovascular stenting with decompressive craniectomy for life-threatening intracranial bleeding with herniation with near-complete recovery.
Kearns-Sayre syndrome is a rare mitochondrial deletion syndrome characterized by triad of cardiac conduction defects, chronic progressive external ophthalmoplegia and pigmentary retinopathy. We present a 15 years old child who was diagnosed and treated as myasthenia gravis for several years and currently presented with complete heart block. He was finally diagnosed as having KSS on mitochondrial genome sequencing analysis. Thus, KSS and MG are mimics and a high suspicion of KSS should be kept in patients who are diagnosed as MS and additionally have cardiac problems.
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