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encephalocele/œdème
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Fetus with asymmetric parietal encephalocele, and hydrops secondary to laryngeal atresia.
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We describe a fetus with an asymmetric, nonmidline, parietal encephalocele that appeared to result from "expulsion" through the center of the membranous bone; the fetus also had laryngeal atresia, which caused pulmonary overdistension (fetal Valsalva maneuver) with consequent hydrops fetalis. A
Mucormycosis Leading to Cerebral Edema and Cerebellar Tonsillar Herniation after Allogeneic Bone Marrow Transplant: A Case Report.
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Delayed Cerebral Edema Leading to Cerebral Hernia in a Patient With Heroin Overdose.
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Prenatal sonographic diagnosis of scalp edema/cephalohematoma mimicking an encephalocele.
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Prenatal skin edema mimicking a recurrence of meningo-encephalocele.
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Mediastinal teratoma as a rare cause of hydrops fetalis and death: report of 3 cases.
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BACKGROUND
Congenital mediastinal teratomas are rare and may present with nonimmune hydrops. The lesion may be misinterpreted on ultrasound.
METHODS
A 21-year-old woman, gravida 2, para 0111, was evaluated at 19 4/7 weeks of gestation for suspected fetal death. An ultrasonogram confirmed the death
Racking the brain: detection of cerebral edema on postmortem computed tomography compared with forensic autopsy.
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OBJECTIVE
The purpose of this study was to compare postmortem computed tomography with forensic autopsy regarding their diagnostic reliability of differentiating between pre-existing cerebral edema and physiological postmortem brain swelling.
METHODS
The study collective included a total of 109
Identification and Treatment of the Early Form of Neurogenic Pulmonary Edema in Emergency Room.
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To improve the management of the early neurogenic pulmonary edema(NPE)in patients with non-traumatic cerebral hemorrhage.
Totally 140 eligible patients with non-traumatic cerebral hemorrhage who were treated in the emergency department of our hospital from October 2008 to October 2014 were divided
Peculiar venous lesions in fatal hyponatremic brain edema.
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A 19-year-old woman with a 3-year history of schizophrenia suddenly began to vomit, and rapidly developed a coma an hour after the onset of vomiting. A brain CT scan showed diffuse brain edema with compression of the ventricles. Laboratory tests showed a low serum sodium concentration of 117 mmol/L.
Tonsillar Herniation After Lumbar Puncture in Idiopathic Intracranial Hypertension.
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A 30-year-old woman with coexisting renal tubular acidosis and idiopathic intracranial hypertension (IIH), treated with acetazolamide, experienced coning (cerebellar tonsillar herniation) after a lumbar puncture (LP). Brain magnetic resonance imaging at initial diagnosis of IIH showed minor
Cerebellar herniation after lumbar puncture in galactosemic newborn.
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Cerebral edema resulting in elevated intracranial pressure is a well-known complication of galactosemia. Lumbar puncture was performed for the diagnosis of clinically suspected bacterial meningitis. Herniation of cerebral tissue through the foramen magnum is not a common problem in neonatal
Unusual, Acute, and Delayed Traumatic Torcular Herophili Epidural Hematoma Causing Malignant Encephalocele During Surgery: A Case Report.
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BACKGROUND Traumatic torcular herophili epidural hematoma is a rare and specific type of traumatic brain injury that is technically difficult to treat and, more critically, can lead to malignant encephalocele during the operation. CASE REPORT A 40-year-old man presented to our hospital 2 h after a
Hypersomnia due to injury of the ventral ascending reticular activating system following cerebellar herniation: A case report.
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BACKGROUND
We report on a patient with hypersomnia who showed injury of the lower ascending reticular activating system (ARAS) following cerebellar herniation due to a cerebellar infarct, detected on diffusion tensor tractography (DTT).
UNASSIGNED
A 53-year-old male patient was diagnosed as a left
Cervicomedullary injury after pneumococcal meningitis with brain edema.
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OBJECTIVE
To demonstrate a rare but potential mechanism of quadriplegia in a patient with fulminant pneumococcal meningitis complicated by severe intracranial hypertension.
METHODS
Case report.
METHODS
Intensive care unit.
METHODS
A 21-year-old man who presented with 3 days of headache,
A case of achondrogenesis type IA with an occipital encephalocele.
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We report on a case of achondrogenesis type IA (Houston-Harris) with an occipital encephalocele. Prenatal sonograms revealed polyhydramnios, subgaleal edema, microcephaly, a narrow thorax, pericardial effusion, and a severe short-limbed dwarfism with unossified tubular bones and vertebral bodies.
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