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                                                                           Chapter 3: Respiratory oncology 137


                    no involvement of the heart, great vessels, trachea,  Clinical features

                    oesophagus or vertebrae.                    The tumour can present with obstruction, recurrent
                    no malignant pleural effusion.              haemoptysis or with metastatic disease. There may be

                    no contralateral node involvement.          weight loss.

                    no distant metastases (chest CT, serum alkaline phos-

                    phatase).
                                                                Macroscopy/microscopy
                    adequate lung function (FEV 1 > 1.5 L, gas transfer

                                                                They arise from lobar or segmental bronchi into which
                    >50% normal).
                                                                they protrude as a rounded mass usually covered by in-
                  Surgery (only usually possible in 25%) involves the re-
                                                                tact epithelium. Cells are cuboidal, arranged in a mosaic
                  moval of the anatomical unit containing the tumour
                                                                or trabecular pattern and have a dense core and neurose-
                  (segment,lobeorlung)togetherwiththeassociatedlym-
                                                                cretory granules.
                  phatic drainage. 35–40% 5-year survival rate but closer
                  to 90% with peripheral lesions.
                                                                Complications
                                                                1 Lung collapse and consolidation distal to the obstruc-
                  Prognosis                                      tion.
                    Non-small cell – 20% have successful resection, 10%  2 Local invasion, spread to lymph nodes and distant

                    survive for 5 years. Inoperable non-small cell carci-  metastasis.
                    noma – chemotherapy is effective in ∼20% and at best  3 Rarely, the carcinoid syndrome – recurrent episodes
                    givesasurvivalbenefitofafewmonths,andithastoxic  of a combination of
                    side-effects. Median survival ∼8months with combi-     flushing of the face and neck sometimes leading to
                    nation chemotherapy.                           telangectasia (due to kinins).
                    Small cell carcinoma limited to thorax: Median sur-  abdominal pain, nausea, vomiting and watery di-

                    vival 18–24 months with combination chemotherapy  arrhoea (5HT).
                    and radiotherapy and up to 20% survive 2 years, only     tricuspid regurgitation or pulmonary stenosis.
                    6–12 weeks without treatment. Small cell carcinoma
                    with metastases: Median survival ∼8months with
                                                                Investigations
                    combination chemotherapy, rarely survive to 2 years.     Chest X-ray may show a rounded lesion.
                    The rare alveolar carcinoma carries a poor prognosis     Bronchoscopy usually shows a pedunculated vascular

                    due to its multifocal nature.
                                                                 tumour protruding into the lumen.
                                                                 24-hour urinary excretion of the metabolite of 5HT.

                                                                 (5-hydroxyindoleacetic acid (5-HIAA)) on a low sero-
                  Bronchial carcinoid tumours                    tonindiet(excludingbananas,tomatoes,walnuts,etc.)
                  Definition
                  Arare neuroendocrine tumour of the lung.      Management
                                                                Local resection is indicated in all cases.

                  Pathophysiology
                  These are highly vascular, low-grade malignant tumours  Prognosis
                                                                80% 10-year survival.
                  which are locally invasive and can metastasise. They arise
                  from bronchial enterochromaffin (Kulchitsky) cells, and
                  can secrete various amines and peptides, including  Secondary lung tumours
                  serotonin (5-hydroxytryptamine (5HT)), histamine and
                  bradykinin. These rarely cause the carcinoid syndrome,  Definition
                  as to do so they have to metastasise to the liver first (the  Metastases to the lung are very common due to
                  peptides are metabolised in the liver).       haematogenous spread.
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