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Tracheobronchial neoplasia refers to benign or malignant tumors arising from the trachea and main bronchi. Primary tumors are rare (≈2% of all respiratory tract malignancies), but the tracheobronchial tree is frequently affected secondarily by direct extension or metastasis.

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Etiopathogenesis


Benign Neoplasms

Squamous papilloma / Papillomatosis HPV-related, multiple exophytic lesions, risk of malignant transformation
Hamartoma Composed of cartilage, fat, connective tissue; often incidental
Lipoma, leiomyoma, fibroma Rare mesenchymal tumors
Neurogenic tumors (schwannoma, paraganglioma) Arising from autonomic or paraganglionic tissue

Malignant neoplasms:

Squamous cell carcinoma (SCC) Most common tracheal malignancy. Associated with smoking. Tends to cause irregular, ulcerated intraluminal mass with early obstruction.
Adenoid cystic carcinoma (ACC) Second most common. Arises from submucosal glands, often in younger patients. Shows submucosal infiltration with smooth, long-segment concentric narrowing; tends to spread longitudinally along the airway.
Carcinoid tumors Neuroendocrine origin. Can be typical (low-grade, indolent) or atypical (more aggressive). Commonly endobronchial, causing recurrent pneumonia/atelectasis.
Mucoepidermoid carcinoma Arises from minor salivary glands in tracheobronchial tree; usually low-grade, lobulated enhancing mass.
Small cell carcinoma Rare in trachea, more common in bronchi; aggressive, associated with paraneoplastic syndromes.
Metastatic/secondary involvement From lung, thyroid, esophagus, larynx, or hematogenous spread (renal cell carcinoma, breast, colon)

Clinical Features


Radiology


Chest Radiography

CT (modality of choice)