Annales d'oto-laryngologie et de chirurgie cervico faciale : bulletin de la Societe d'oto-laryngologie des hopitaux de Paris · 2008
[Angiomyolipoma of the parotid gland].
Клинический случайСтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Guevara N, Lassalle S, Castillo L, Butori C, Santini J
Аннотация
INTRODUCTION: Angiomyolipoma is a rare benign mesenchymal tumor. It often arises in the kidney and in association with tuberous sclerosis or lymphangioléiomyomatosis. Extrarenal locations have been described, especially in the liver. Only a few cases have been described in the head and neck region and these are usually not associated with tuberous sclerosis or lymphangioléiomyomatosis.
MATERIAL AND METHODS: We report a case of angiomyolipoma located in the parotid gland.
RESULTS: A 43-year-old man consulted for treatment with a slow-growing nodule located in his right parotid gland. Ultrasound examination and magnetic resonance imaging revealed a well-limited lesion. Fine needle aspiration cytology was not suspicious. Partial parotidectomy was performed and the tumor showed the characteristic appearance of angiomyolipoma, with an admixture of fat smooth cells and tortuous thick-walled blood vessels. Genetic analysis showed anomalies on chromosomes 7 and 18.
CONCLUSION: This article discusses the presentation and management associated with this exceptional tumor.
MATERIAL AND METHODS: We report a case of angiomyolipoma located in the parotid gland.
RESULTS: A 43-year-old man consulted for treatment with a slow-growing nodule located in his right parotid gland. Ultrasound examination and magnetic resonance imaging revealed a well-limited lesion. Fine needle aspiration cytology was not suspicious. Partial parotidectomy was performed and the tumor showed the characteristic appearance of angiomyolipoma, with an admixture of fat smooth cells and tortuous thick-walled blood vessels. Genetic analysis showed anomalies on chromosomes 7 and 18.
CONCLUSION: This article discusses the presentation and management associated with this exceptional tumor.