scholarly journals An Unusual Case of Pericardial Effusion in a Diabetic Patient

2010 ◽  
Vol 55 (6) ◽  
pp. e11 ◽  
Author(s):  
Ian Webb ◽  
Imad Nadra ◽  
Mohamad Faris ◽  
James Roxburgh ◽  
Simon Redwood
2021 ◽  
pp. 004947552110343
Author(s):  
Sapna Sandal ◽  
Gopal Krishnan ◽  
Ashish Sharma ◽  
Javed Ismail ◽  
Jaivinder Yadav

Parasitic infections are the leading cause of hypereosinophilia in the paediatric population in tropical countries. We report an unusual case of Toxocara infection in an eight-year-old boy who presented with intermittent fever, hypereosinophilia complicated by massive pericardial effusion and a mycotic aneurysm. This child received treatment with four weeks of albendazole and steroids.


2009 ◽  
Vol 42 (3) ◽  
pp. 569-573 ◽  
Author(s):  
Abul Ala Syed Rifat Mannan ◽  
Mirza Kahvic ◽  
Naorem Gopendro Singh ◽  
Yahya Abu Sara ◽  
Chandramouli Bharati

Author(s):  
Abhilash Chandra ◽  
Namrata Rao ◽  
Anupam Das ◽  
Manodeep Sen

Background and Purpose: Fungal renal abscesses are rare entities associated with significant morbidity and mortality. Affected kidneys can have microabscess, pyelonephritis, pyonephrosis, or papillary necrosis.Case report: Herein, we reported an unusual case of a large renal abscess cause by Candida tropicalis in a diabetic patient. The entity presented as a lump in the abdomen and later was diagnosed to be an abscess on computed tomography scan. Candida tropicalis was confirmed on the culture of the aspirate. The abscess was successfully treated by percutaneous drainage and administration of amphotericin B deoxycholate.Conclusion: Candida tropicalis is now a global concern because of its rising prevalence and high virulence. The growing resistance of this Candida species to azoles, as in our case, calls for a more judicious usage of antifungal agents. Empirical therapy with either amphotericin or echinocandins is an option in case of high azole resistance. This case highlights the importance of timely diagnosis and implementation of aggressive management in cases suffering from fungal abscesses.


2020 ◽  
Vol 30 (4) ◽  
pp. 571-573
Author(s):  
Jue Seong Lee ◽  
Mi Kyoung Song ◽  
Saebeom Hur

AbstractA 29-month-old girl had idiopathic massive pericardial effusion for over 6 months. Lymphangiography was performed for chronic and recurrent pericardial effusion and pulmonary lymphangiectasia, suspected based on CT findings. Magnetic resonance lymphangiography revealed chylolymphatic reflux from a tortuously dilated thoracic duct in the mediastinum to the pericardial space, suggesting primary chylopericardium with lymphangiectasia. Pericardial effusion resolved immediately after thoracic duct embolisation at the lower thoracic level. However, pericardial effusion recurred after 5 months, which resolved after additional embolisation of the abnormal lymphatic collateral vessels from the remnant upper thoracic duct. Here, we report an unusual case with chylous massive pericardial effusion diagnosed by magnetic resonance lymphangiography and treated with percutaneous embolisation.


2009 ◽  
Vol 18 (5) ◽  
pp. 418-421 ◽  
Author(s):  
Abul Ala Syed Rifat Mannan ◽  
Mirza Kahvic ◽  
Yahya Abu Sara ◽  
Chandramouli Bharati

2017 ◽  
Vol 4 (2) ◽  
pp. 581
Author(s):  
Pavankumar Pyarsabadi ◽  
Manoj Saluja ◽  
Saurabh Chittora ◽  
Yogesh Swami ◽  
Hemanth Richariya ◽  
...  

Pericardial effusion is not so uncommon in hypothyroidism, but pericardial tamponade is very rare entity. Hypothyroidism complicated by pericardial tamponade is very rarely referenced in the medical literature. Here we report a rare case of a 70 year old female, who presented with breathlessness and was found to have hypothyroidism with large pericardial effusion complicating into pericardial tamponade. Management included urgent pericardiocentesis followed by l-thyroxine supplementation.


2017 ◽  
Vol 38 (suppl_1) ◽  
Author(s):  
S. Palacio Restrepo ◽  
M. Imazio ◽  
P. Ferrazzi ◽  
I. Binaco ◽  
M.L. Fibbi ◽  
...  

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