Đang chuẩn bị liên kết để tải về tài liệu:
Báo cáo y học: "Mucoepidermoid carcinoma of the lung: a case report"

Đang chuẩn bị nút TẢI XUỐNG, xin hãy chờ

Tuyển tập các báo cáo nghiên cứu về y học được đăng trên tạp chí y học Wertheim cung cấp cho các bạn kiến thức về ngành y đề tài: Mucoepidermoid carcinoma of the lung: a case report. | Kitada et al. Journal of Cardiothoracic Surgery 2011 6 132 http www.cardiothoracicsurgery.Org content 6 1 132 JCTS JOURNAL OF CARDIOTHORACIC SURGERY CASE REPORT Open Access Mucoepidermoid carcinoma of the lung a case report 1 1 1 11 2 Masahiro Kitada Yoshinari Matsuda Kazuhiro Sato Satoshi Hayashi Kei Ishibashi Naoyuki Miyokawa and Tadahiro Sasajima1 Abstract Mucoepidermoid carcinoma of the lung MEC is a tumor of low malignant potential of bronchial gland origin. MEC and adenoid cystic carcinoma are both considered to be salivary gland-type neoplasms. MECs are comparatively rare with an incidence of all lung cancers. We recently encountered a case of this type of lung cancer. A 60-year-old man was found to have an abnormal shadow in the left lower lung field on a regular checkup for lung cancer at his company. Chest radiography and CT revealed a mass shadow measuring 30 mm in diameter in the left lower lung field. Bronchoscopy revealed a protuberant tumor in the S9 bronchus leading to a diagnosis of low-grade MEC by transbronchial lung biopsy. He underwent left lower lobe resection and mediastinal lymph node dissection using VATS. Tumor cells had a scattering of mucus-producing epithelial components in papillary growth of stratified squamous epithelia with anisokaryosis and minimal pleomorphism indicating a diagnosis of MEC. Because the postoperative course was good and the tumor was low-grade no adjuvant treatment was administered. The patient has had no signs of tumor recurrence for 9 months to date since resection of the tumor Introduction Mucoepidermoid carcinoma of the lung MEC is a tumor of low malignant potential of bronchial gland origin. MEC and adenoid cystic carcinoma are both considered to be salivary gland-type neoplasms. MECs are comparatively rare with an incidence of 0.1 -0.2 of all lung cancers occurring mostly in young persons. MECs proliferate in a polyp-like form in the central bronchial lumen up to the segmental bronchus level. We report a case

TÀI LIỆU LIÊN QUAN