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    Arterial spasm following perimesencephalic nonaneurysmal subarachnoid hemorrhage in a pediatric patient
    (ELSEVIER SCIENCE INC, 2005) Sert, A; Aydin, K; Pirgon, O; Emlik, D; Ustun, ME
    Perimesencephalic nonaneurysmal hemorrhage is a benign form of subarachnoid hemorrhages. This entity is well recognized as a distinct type of subarachnoid hemorrhage in adults. However, perimesencephalic nonaneurysmal subarachnoid hemorrhage in pediatric patients is not well recognized. Angiographic changes such as vasospasm are uncommon in patients, especially in pediatric patients suffering from this type of hemorrhage. This case study reports a 12-year-old male who suffered from perimesencephalic nonaneurysmal subarachnoid hemorrhage. Cerebral carotid angiography performed on the tenth day of the posthemorrhagic period revealed severe vasospasm affecting the basilar artery. The patient, treated symptomatically, was discharged after improvement. One year later, magnetic resonance angiography revealed completely normal features. (c) 2005 by Elsevier Inc. All rights reserved.
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    Oral alendronate therapy for severe vitamin D intoxication of the infant with nephrocalcinosis
    (FREUND PUBLISHING HOUSE LTD, 2006) Atabek, ME; Pirgon, O; Sert, A
    Vitamin D intoxication is a well-known cause of hypercalcemia in children. We report here the use of oral alendronate for the treatment of hypercalcemia due to vitamin D intoxication in a 7 month-old infant with nephrocalcinosis. The serum calcium levels were normalized without complications. Oral alendronate therapy may be safely used in hypercalcemia due to vitamin. D intoxication in pediatric patients with nephrocalcinosis resistant to hydration, diuretics or corticosteroids.
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    Zimmermann-Laband syndrome in an infant with an atypical histologic finding
    (SPRINGER, 2005) Atabek, ME; Pirgon, O; Sert, A; Toy, H
    Zimmermann-Laband syndrome is an inherited disorder that is characterized by abnormalities of the head, face, hands, and feet. Most children with this disorder have generalized hypertrichosis, large gingivae, and hypoplasia of the fingernails and toenails. We report a male infant who exhibited typical features of Zimmermann-Laband syndrome with an unusual histopathologic finding. Excised tissue from the infant's gingivae showed papillary projections that were composed of hyperplastic stratified squamous epithelium with different amounts of keratinization.