Objectives: To describe a group of patients with thymoma who were submitted to surgica treatment associated or not with therapy, and evaluate their prognosis. Methods: Of the 104 patients with thymic tumors who were operated at Hospital das Clínicas - São Paulo University Medical School between 1965 and 1998, (66.3%) were males. Mean age at diagnosis, was 47.9% ± 16.3 years (ranging from 13 to 76 years). Results: Of the 104 patients, 89 (85.6%) underwent complete thymoma resection, 6 (5.8%) underwent partial resection and, in 9 (8.6%) of them, biopsy was performed. Anatomopathologic diagnosis (thymoma vs malignant thymoma) and the type of surgery (biopsy vs complete resection vs partial resection) were significant predictors of survival mean time (p < 0.02). Conclusions: Complete resection is the treatment of choice for thymomas. These tumors, when not invasive and completely resected, have good immediate and late prognosis.

Keywords: Thymoma.

Background: Pulmonary sequestration is a congenital anomaly involving the pulmonary parenchyma and its vascularization, and it presents as extralobar or intralobar. Aim: Describe the cases treated at the Institute of Heart (InCor) and Clinical Hospital of the Medical School of the University of São Paulo (FMUSP). Method: Retrospective analyses of the files of the patients treated over the 10-year period taking demographic, clinical and laboratorial data. Results: The patients were recurrent pulmonary infection and hemoptysis were frequent clinical findings in these patients. All cases were intralobar. The main localization was the left lower lobe (66%). Only one diagnosis was made intra-operatively. In the other eight cases, diagnosis was suggested on chest radiographs (100%) and confirmed by angiography (77%) and computed tomography (66%). Lobectomy (77%) was the most common surgical treatment, with low post-operative morbidity, and no mortality. Anatomic and histologic examination was performed in seven cases and confirmed the pathology. Conclusion: Pulmonary sequestration is an uncommon entity, in which the computed tomography and the angiography are the radiological investigations that provide the most information to a definitive and secure diagnosis. Resection of the involved tissue leads to excellent results.

Primitive neuroectodermal tumor is an invasive neoplasm with neuronal differentiation, which frequently results in metastasis in various organs. We report the case of a patient with primitive neuroectodermal tumor whose primary site was the axilla. The patient presented with metastases in the lung, pleura, bone, iliac muscle and bone marrow. We highlight the uncommon finding in the pleural fluid cytology.

Keywords: Neuroectodermal tumors, primitive; Neoplasm metastasis; Cytology; Pleural effusion.