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Pulmonary carcinoid is a rare type of lung cancer that originates in the neuroendocrine cells of the lung. It accounts for about 1-2% of all lung cancers. Types: 1. Typical carcinoid (TC): Low-grade, slow-growing 2. Atypical carcinoid (AC): Intermediate-grade, moderately aggressive 3. Large cell neuroendocrine carcinoma (LCNEC): High-grade, aggressive 4. Small cell lung cancer (SCLC): High-grade, aggressive Symptoms: 1. Coughing 2. Chest pain 3. Shortness of breath 4. Wheezing 5. Coughing up blood 6. Weight loss 7. Fatigue Diagnosis: 1. Imaging tests (CT, MRI, PET scans) 2. Biopsy (bronchoscopy, fine-needle aspiration) 3. Histopathological examination 4. Immunohistochemistry (IHC) staining Treatment: 1. Surgery (lobectomy, pneumonectomy) 2. Chemotherapy 3. Radiation therapy 4. Targeted therapy (somatostatin analogs) 5. Octreotide scanning Prognosis: 1. Typical carcinoid: 90-100% 5-year survival 2. Atypical carcinoid: 50-70% 5-year survival 3. Large cell neuroendocrine carcinoma: 20-40% 5-year survival 4. Small cell lung cancer: 5-10% 5-year survival Note: Pulmonary carcinoid is a complex condition, and treatment decisions should be made in consultation with a healthcare professional. #Pulmonarycarcinoid