Bronchial Adenoma Clinical Presentation
- Author: Charles W Van Way III, MD; Chief Editor: Zab Mosenifar, MD more...
History
Up to 60% of patients have no symptoms. This is more likely if the adenoma is located peripherally as opposed to proximally. When present, symptoms are related to the presence and degree of endobronchial occlusion and the vascularity of the tumor. Hemoptysis occurs in 18%, recurrent infection or cough in 17%, dyspnea or wheezing in 2%, and carcinoid syndrome in 1%.
Endobronchial symptoms
- Classic triad of cough, hemoptysis, and recurrent infection
- Dyspnea
- Wheezing and stridor
- Sputum production
- Pneumonia
Mediastinal involvement
- Hoarseness due to recurrent laryngeal nerve involvement
- Chylothorax due to thoracic duct involvement
- Chest pain
Systemic
- Endocrinopathies
- Unexplained weight loss
- Low-grade temperature elevation
Classic triad of symptoms
- Cough
- Hemoptysis
- Recurrent infection
Physical
Physical examination generally is unrevealing, but subtle findings may provide clues. In addition, the physical examination may help in finding other confounding disease processes.
Upper airway obstruction - Stridor/wheezing
- Lower airway obstruction
- Asymmetric breath sounds
- Postobstructive processes
Respiratory insufficiency
- Dyspnea
- Increased work of breathing
- Retractions
- Orthopnea
- Cyanosis
Extrapulmonary manifestations
These are rare, but may include mechanical compressive and obstructive syndromes such as those seen in other thoracic malignancies.
- Pancoast tumor - Superior sulcus tumor causing pain (eg, shoulder, forearm, arm, scapula), Horner syndrome, and atrophy of upper extremity musculature
- Acute spinal cord compression – Paraplegia, sensory deficits, urinary retention/incontinence, and vertebral pain
- Superior vena cava syndrome – Head congestion/fullness; headache; nasal congestion; dyspnea; cough; orthopnea; dilated veins in the upper extremity, neck, and face; upper extremity and facial edema; papilledema; facial cyanosis; and mental status changes
Causes
Bronchial carcinoids are thought to arise from Kulchitsky cells. These neuroendocrine cells, formerly classified as amine precursor uptake and decarboxylation cells, produce and store biogenic amines and peptides. Typical carcinoids originate as clusters of monotonous polyhedral cells in a fibrovascular stroma. Ultrastructurally and immunoreactively, carcinoids share characteristics with small cell neuroendocrine carcinoma of the lung.
Adenoid cystic carcinoma originates from salivary gland tissue. Occasionally, some tumor cells in this variant are of myoepithelial origin. These tumors have several other names, including cylindromas, adenoid cystic basal cell carcinomas, adenomyoepitheliomas, and pseudoadenomatous basal cell carcinomas.
Mucoepidermoid carcinomas originate from tracheal and proximal bronchi. These tumors are of squamous and intermediate elements, with intercellular bridges. They have the same microscopic appearance as mucoepidermoid carcinoma of the salivary glands, arise in glandular submucosa, and manifest as submucosal lesions.
Mucous gland adenomas (ie, bronchial cysts, papillary cystadenomas) are rare submucosal tumors arising from mucous glands and truly are benign tumors.
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