Experience with Surgical Excision in Childhood Pheochromocytoma
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چکیده
منابع مشابه
Experience with Surgical Excision in Childhood Pheochromocytoma
Pheochromocytoma is one of the potentially fatal causes of childhood hypertension. The study aims to analyze the results of our experiences in pheochromocytomas and the long-term results of its surgical treatment in children. The records of 15 children (11 boys, 4 girls) treated for pheochromocytoma in our unit during the period of 1984 and 2002 were reviewed retrospectively. The average age at...
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Background: Bowen’s disease is a form of intraepidermal squamous cell carcinoma (SCC) characterised by a persistent, non-elevated, red, scaly or crusted plaque with a small potentialfor invasive malignancy. Most cases of typical Bowen’s disease in the white population are found on the lower legs of the elderly women. H...
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Pheochromocytoma is a neoplasia of chromaffin cells that is very rare in children. Its signs and symptoms result from the release of catecholamines. We report the case of a child with pheochromocytoma of difficult clinical management, confirmed on the anatomicopathological study, and cured after surgical resection.
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BACKGROUND Keloids as unusual scars are injury remnants characterized by bizarre cosmetics and painful itching. This study assessed outcomes of surgical excision and brachytherapy in intractable keloids. METHODS Six patients with 10 keloid lesions were followed up. Surgical excision was done with 1-2 mm margin, and then radiotherapy was undertaken in 3 divided fractions on days 0, 1 and 2 ...
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Case Description- An eight-year-old, light brown and crossbred stallion in a horse-racing club had two gray skin masses on his left thigh and thoracic inlet with a slow growth since two years ago. The masses were 5×7 cm in size, irregular shaped with some convex parts. Surface bleeding had been reported occasionally. CBC and WBC were within normal values. General clinical examination of the...
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ژورنال
عنوان ژورنال: Journal of Korean Medical Science
سال: 2004
ISSN: 1011-8934
DOI: 10.3346/jkms.2004.19.3.401