Titlebook: Atlas of Neoplastic Pulmonary Disease; Pathology, Cytology, Armando E. Fraire,Philip T. Cagle,Megan K. Dishop Book 2010 Springer-Verlag US

configuration

Adenoid Cystic Carcinomaharacteristic predilection for the lateral and posterolateral walls at the junction of the cartilaginous tissue and the posterior connective tissue membrane. Growing into the lumen, the tumors may adopt a lobulated, polypoid, or fusiform appearance. The mucosal surfaces may be highly vascularized.

surmount

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Modicum

Chronic

Congenital Pulmonary Myofibroblastic Tumorrine fetal demise, hydrops fetalis, or severe respiratory distress at birth. Approximately 10 cases of CPMT have been described in the literature, including cases reported under names such as “bronchopulmonary leiomyosarcoma,” “bronchopulmonary fibrosarcoma,” and “congenital fibroleiomyosarcoma.” Th

expansive

Malfunction

Meager

Pleomorphic Adenomafrom seromucinous glands of the airway and are similar to those seen in major salivary glands. These tumors are more frequent in men by a factor of about 2:1 with a mean age of 50 years. Productive cough and intermittent dyspnea are manifestations of tracheal tumors. Other symptoms are wheezing, res

Guileless

BATE

Adenoid Cystic Carcinoma histopathologic patterns and a propensity for extension along perineural spaces. Asthma-like manifestations with wheezing as a prominent sign can be seen in proximally located lesions. Ulceration of the overlying mucosa may result in blood-tinged sputum or frank hemoptysis while atelectasis is more