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1.
Diagn Cytopathol ; 44(8): 696-9, 2016 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-27177687

RESUMO

Pulmonary hydatid cyst with co-existing aspergillosis is rare. Till date, there are only two documented reports of this double pathology being diagnosed on cytology. The present case is of a young immunocompetent female who presented with respiratory complaints including intermittent hemoptysis. Chest X-ray and CT thorax revealed two well-defined lesions in the lower lobe of left lung that was suggestive of either infective or benign neoplastic etiology. But as hydatid cyst was not suspected either clinically or radiologically, FNA was performed. Based on the typical cytomorphological features a definitive diagnosis of hydatid cyst with aspergillosis was offered on cytology that was later confirmed on histopathology. To the best of our knowledge this is only the third report of pulmonary echinococcosis with aspergillus co-infection being diagnosed on cytology. The purpose of reporting this case is to draw attention to the rare possibility of co-existing aspergillus infection in pulmonary echinococcosis even in immunocompetent individuals, which can complicate the clinico-radiological picture. However, both pathologies can be effectively and accurately diagnosed on cytology, based on which proper treatment can be initiated. Diagn. Cytopathol. 2016;44:696-699. © 2016 Wiley Periodicals, Inc.


Assuntos
Equinococose Pulmonar/patologia , Aspergilose Pulmonar/patologia , Adulto , Biópsia por Agulha Fina , Equinococose Pulmonar/complicações , Equinococose Pulmonar/diagnóstico por imagem , Feminino , Humanos , Aspergilose Pulmonar/complicações , Aspergilose Pulmonar/diagnóstico por imagem , Tomografia Computadorizada por Raios X
2.
Heart Lung Circ ; 21(5): 287-8, 2012 May.
Artigo em Inglês | MEDLINE | ID: mdl-21890408

RESUMO

Detection of a rapidly growing mass in the right atrium during routine inter-echocardiogram follow-up period in two patients after corrective open-heart surgery raises concerns about nature of the mass and the probable cause. One turned out to be an atrial myxoma that grew rapidly over a eight month period and the other a well encapsulate thrombus in a fully anticoagulated patient. Preoperative transthoracic echocardiogram had reported both the cases to be a myxoma. This article highlights the importance of considering rare causes in the face of a seemingly obvious diagnosis and possible use of imaging modalities in the management of these cases.


Assuntos
Átrios do Coração/patologia , Neoplasias Cardíacas/cirurgia , Mixoma/cirurgia , Trombose/cirurgia , Adolescente , Adulto , Ecocardiografia , Neoplasias Cardíacas/diagnóstico , Neoplasias Cardíacas/etiologia , Humanos , Masculino , Mixoma/diagnóstico , Mixoma/diagnóstico por imagem , Complicações Pós-Operatórias , Período Pós-Operatório , Trombose/diagnóstico , Trombose/etiologia , Adulto Jovem
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