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1.
J Med Case Rep ; 4: 164, 2010 May 28.
Article in English | MEDLINE | ID: mdl-20509900

ABSTRACT

INTRODUCTION: Congenital cystic adenomatoid malformation of the lung is an uncommon cause of respiratory distress in neonates and babies. The disorder is usually diagnosed in the neonatal period and the first two years of life. This anomaly has been described in association with bronchopulmonary sequestration, extralobar intra-abdominal sequestration or bronchial atresia in live and stillborn babies. It is rarely encountered in adults, in whom the diagnosis is made incidentally from mass lesion features seen on chest radiographs. The oldest patients recorded with this malformation have been about 35 years old, and only 10% of primary diagnoses are made after the first year of life. Delayed diagnosis can be related to infection or serendipitous discovery. CASE PRESENTATION: We describe the radiological findings of a 34-year-old Caucasian woman with a clinical history of recurrent pneumonia, intermittent anterior pleuritic chest pain and haemoptysis. Congenital cystic adenomatoid malformation of the lung associated with bronchial atresia involving a different lobe was discovered. CONCLUSION: Although rare in adults, congenital cystic adenomatoid malformation should be suspected in adult patients who suffer from recurrent or persistent non-productive coughs. The discovery of an association of congenital cystic adenomatoid malformation with bronchial atresia in adulthood is rare but possible, even in different lobes.

2.
J Thorac Imaging ; 24(1): 41-4, 2009 Feb.
Article in English | MEDLINE | ID: mdl-19242303

ABSTRACT

We report the case of pulmonary benign metastasizing leiomyoma in an asymptomatic 64-year-old woman who underwent hysterectomy for a uterine leiomyoma 26 years earlier. Routine chest radiograph revealed bilateral diffuse nodular opacities within the pulmonary lobes. Thoracic computed tomography (CT) scan showed peripheral lung nodules that do not display contrast enhancement. Positron emission tomography (PET)-CT with 18F-fluorodeoxyglucose (18F-FDG PET-CT) demonstrated no significant metabolic activity of the nodules. The lesions were diagnosed as benign metastasizing leiomyoma by histopathologic examination. To our best knowledge, this is the first case studied combining CT and FDG PET-CT technique.


Subject(s)
Leiomyoma/diagnostic imaging , Lung Neoplasms/diagnostic imaging , Tomography, Emission-Computed/methods , Biopsy, Needle , Contrast Media , Female , Fluorodeoxyglucose F18 , Humans , Lung Neoplasms/secondary , Middle Aged , Radiopharmaceuticals , Tomography, X-Ray Computed , Uterine Neoplasms/pathology
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