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1.
Rev. méd. Chile ; 147(9): 1206-1209, set. 2019. graf
Article in Spanish | LILACS | ID: biblio-1058665

ABSTRACT

Adventitial cystic disease of the popliteal artery is a rare condition of uncertain etiology, which presents as intermittent claudication of the lower extremity in middle-age patients. We report a 44-year-old man presenting with intermittent claudication of his left leg. MR angiography showed cystic parietal lesions that caused compression with partial occlusion of the left popliteal artery. Surgical resection of the affected segment was performed, with venous graft interposition. The histopathological analysis of the surgical specimen was consistent with cystic adventitial disease.


Subject(s)
Humans , Male , Adult , Middle Aged , Cysts/complications , Cysts/diagnostic imaging , Intermittent Claudication/etiology , Popliteal Artery/diagnostic imaging , Angiography , Leg
2.
Rev. méd. Chile ; 147(5): 663-667, mayo 2019. tab, graf
Article in Spanish | LILACS | ID: biblio-1014276

ABSTRACT

We report a 64 years old female admitted with fever, cough, dyspnea and lung opacities in the chest X ray. A chest tomography scan (CTS) showed multiple-bilateral ring-shaped opacities and the reversed halo sign (RHS). The patient did not improve with antimicrobial therapy (AT). Infection and rheumatologic causes were excluded, therefore Cryptogenic organizing pneumonia (COP) was suspected with compatible percutaneous biopsy. Systemic steroids were started with a good clinical response. The patient was discharged four weeks after admission in good general conditions and practically no lungs opacities.


Subject(s)
Humans , Female , Middle Aged , Cryptogenic Organizing Pneumonia/pathology , Cryptogenic Organizing Pneumonia/diagnostic imaging , Biopsy , Prednisone/therapeutic use , Radiography, Thoracic , Tomography, X-Ray Computed , Cryptogenic Organizing Pneumonia/drug therapy , Glucocorticoids/therapeutic use , Lung/pathology , Lung/diagnostic imaging
3.
Rev. méd. Chile ; 146(10): 1102-1111, dic. 2018. tab, graf
Article in Spanish | LILACS | ID: biblio-978745

ABSTRACT

Background:: Pulmonary cystic nodules are a relatively frequent finding in chest computed tomography (CT). There is a possible association between this finding and lung cancer. Aim: To report eight patients with malignant lung cystic lesions. Material and Methods: Retrospective analysis of images in a CT database from 2007 to 2015, looking for cystic lesions of the lung with wall thickening, whose pathological diagnosis was lung cancer. Results: We identified eight patients with cystic nodules aged 44 to 77 years, of which five were women. Six were active and two former smokers. The pathological diagnosis was adenocarcinoma in seven cases and squamous cell in one. The mean diameter of the cystic lesions was 11.5 mm. The mean diagnostic delay time was 871 days (range 0-1592). The main finding was a gradual thickening of the nodule walls. Conclusions: The presentation of lung cancer as cystic nodules is uncommon. In this series, the change in morphology due to a thickening of the walls with or without a diameter increase, was the clue for the diagnosis.


Subject(s)
Humans , Male , Female , Adult , Middle Aged , Aged , Carcinoma, Squamous Cell/pathology , Adenocarcinoma/pathology , Cysts/pathology , Lung Neoplasms/pathology , Biopsy , Carcinoma, Squamous Cell/diagnostic imaging , Adenocarcinoma/diagnostic imaging , Smoking/adverse effects , Retrospective Studies , Cysts/diagnostic imaging , Tumor Burden , Positron Emission Tomography Computed Tomography , Lung Neoplasms/diagnostic imaging
4.
Rev. chil. infectol ; 30(6): 669-672, dic. 2013. ilus
Article in Spanish | LILACS | ID: lil-701717

ABSTRACT

Treatment failure in community-acquired pneumonia is defined as a clinical condition with inadequate response to antimicrobial therapy. Resistant and unusual microorganisms and noninfectious causes are responsible for treatment failure. Coccidioides immitis is a fungus that causes pneumonia in the northern hemisphere, especially in the United States and northern Mexico. We report a case of pulmonary coccidioidomycosis imported from Mexico to Chile. After a comprehensive study, histopathology was able to establish Coccidiodes immitis as the causative agent, achieving clinical and radiological improvement with antifungal therapy.


La neumonía de evolución tórpida son aquellas en que no se logra una respuesta clínica adecuada con el uso de terapia antimicrobiana. Existen múltiples causas a esta falta de respuesta: resistencia antimicrobiana, microorganismos no cubiertos o infecciones por microorganismos atípicos. Coccidioides immitis es un hongo causante de neumonía en el hemisferio norte, especialmente en E.U.A y norte de México. No existen reportes de casos pulmonares importados en Chile. Presentamos el caso de una mujer adulta con una neumonía que no respondió al tratamiento antimicrobiano habitual. Una vez realizado un estudio exhaustivo, se logró establecer mediante el estudio histopatológico la existencia de una coccidiodomicosis como entidad causal, logrando una respuesta clínica y radiológica favorable al tratamiento antifúngico.


Subject(s)
Female , Humans , Middle Aged , Coccidioidomycosis , Lung Diseases, Fungal , Antifungal Agents/therapeutic use , Chile , Coccidioidomycosis/diagnosis , Coccidioidomycosis/drug therapy , Community-Acquired Infections/diagnosis , Community-Acquired Infections/drug therapy , Community-Acquired Infections/microbiology , Diagnosis, Differential , Lung Diseases, Fungal/diagnosis , Lung Diseases, Fungal/drug therapy , Lung Diseases, Fungal/microbiology , Mexico , Pneumonia/diagnosis , Travel , Treatment Failure
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