MedElevator Войти в исследования
← Поиск публикаций

DOI 10.5146/tjpath.2012.01106

Медицинская библиотека · Turk patoloji dergisi · 2012

Carcinosarcoma of the lung associated with neurofibromatosis type 1: a case report.

Cıtıl Rana, Ciralik Harun, Karsligıl Ahmet, Oltulu Pembe, Yenıbertız Derya, Sayar Hamide, Gürbüz Esma

Клинический случайСтатьяПеревод пока не подготовлен

Аннотация

Neurofibromatosis or von Recklinghausen's disease is the most common inherited syndrome predisposing to neoplasia. Carcinosarcoma is a rare malignant mixed tumor of the lung. Association of carcinosarcoma of lung with Neurofibromatosis-1 is not common. A 57-year-old man presented with history of fever, cough, hemoptysis, breathlessness, weight loss, chest pain. Multiple cutaneous neurofibromas and café au lait spots were revealed by physical examination. A homogeneous opacity was found in the right middle and right upper zone on posterior-anterior chest radiography. A 8x8x7 cm mass that had irregular borders in right upper posterior and apical segment was seen on contrast enhanced chest computed tomography. On bronchoscopy, the lumen of right upper apical segment was obstructed with vegetating tumoral lesion. The biopsy taken from this region was diagnosed as carcinosarcoma by histopathological and immunohistochemical examination.A rare case with carcinosarcoma of the lung and Neurofibromatosis-1 was reported.

Для цитирования: Cıtıl Rana, Ciralik Harun, Karsligıl Ahmet, Oltulu Pembe, Yenıbertız Derya, Sayar Hamide, Gürbüz Esma. Carcinosarcoma of the lung associated with neurofibromatosis type 1: a case report.. Turk patoloji dergisi. 2012. DOI: 10.5146/tjpath.2012.01106.

Предметные рубрики MeSH

Подготовка и перевод публикации
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

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.

Тип публикации указан по данным источника. Уровень доказательности автоматически не присваивается.