scholarly journals INOPERABLE DISSEMINATED PULMONARY AND PLEURAL CYSTIC HYDATIDOSIS PRESENTING WITH AN OPAQUE HEMITHORAX IN A 14-YEAR-OLD CHILD

2017 ◽  
Vol 2 (4) ◽  
pp. 219-222
Author(s):  
Firas Alakhras Aljanadi
Author(s):  
Arshed Hussain Parry ◽  
Mujahed Abdulsattar Ibrahim Raheem ◽  
Hussam Hassan Ismail ◽  
Osama Sharaf

Abstract Background Pulmonary agenesis is a rare congenital anomaly with a reported prevalence of about 1 in 100,000 births. It may be bilateral or unilateral. Among the unilateral form, left lung agenesis is more common (70%); however, it is the right lung agenesis which carries a dismal prognosis due to the frequent association with a gamut of other congenital anomalies and greater degree of mediastinal shift leading to tracheo-bronchial and vascular distortion. The patients of unilateral pulmonary agenesis usually present in infancy or early childhood. Presentation in late adulthood as seen in our patient is rare. We present a case of left pulmonary agenesis that was diagnosed in 4th decade of life. Case presentation A 36-year-old male presented with gradually progressive exertional dyspnea of 1 month duration. Clinical examination revealed tachycardia and tachypnea. Chest radiograph showed opaque left hemithorax with ipsilateral mediastinal shift. Computed tomography clinched the diagnosis by demonstrating absence of left main bronchus, lung and left pulmonary artery with shift of heart, and great mediastinal vessels into left hemithorax. The patient was managed conservatively and discharged with attachment to out-patient department for regular follow-up. Conclusion Presentation of unilateral lung agenesis in late adulthood, as seen in the present case is extremely rare. This case report highlights that, a rare condition like unilateral pulmonary agenesis, should be considered in the list of differentials in an adult presenting with opaque hemithorax with ipsilateral mediastinal shift on radiography.


2019 ◽  
Vol 7 (5) ◽  
pp. 505-512
Author(s):  
Muslimah, N. ALsulami ◽  
◽  
Nafisa Mohammd Batarfi ◽  

2012 ◽  
Vol 66 (7) ◽  
pp. 192 ◽  
Author(s):  
Soumya Bhattacharjee ◽  
Jaydip Deb ◽  
Arunabha Dattachaudhuri ◽  
Aparup Dhua ◽  
Priyanka Ghosh ◽  
...  

1989 ◽  
Vol 62 (742) ◽  
pp. 951-952 ◽  
Author(s):  
M. F. Creagh ◽  
L. M. MacDonald ◽  
D. C. Garvie
Keyword(s):  

2008 ◽  
Vol 75 (10) ◽  
pp. 1003-1007 ◽  
Author(s):  
D. Tatar ◽  
G. Senol ◽  
E. Gunes ◽  
S. Unsal ◽  
G. Perim

2002 ◽  
Vol 30 (2) ◽  
pp. 206-209 ◽  
Author(s):  
İ Çapoğlu ◽  
N Ünüvar ◽  
F Erdogan ◽  
O Yilmaz ◽  
M Çaydere

Echinococcosis, although eradicated in many countries, is still widespread in communities in which agriculture is dominant, and cystic hydatidosis is a significant public health problem in regions where echinococcosis is endemic. Hydatid cysts may be found in almost any part of the body, but most often in the liver and lungs. Other organs affected occasionally include the brain, muscle, kidney, bone, heart and pancreas. This report documents a rare case with a cystic nodule in the thyroid detected by ultrasonography. The patient was a 40-year-old woman with an euthyroid multinodular goitre. Ultrasonography revealed a cystic nodule, and the ultrasonic appearance of the cyst liquid showed multiple echoes, suggesting that the nodule could be a hydatid cyst. Bilateral subtotal thyroidectomy was performed. Postoperative examination of the nodule showed it to be a solitary primary thyroid hydatid cyst.


1985 ◽  
Vol 78 (7) ◽  
pp. 805-809 ◽  
Author(s):  
LINDA J. WELLNER ◽  
DONALD R. KIRKS ◽  
DAVID F. MERTEN ◽  
BRENDA E. ARMSTRONG
Keyword(s):  

Respiration ◽  
2010 ◽  
Vol 79 (2) ◽  
pp. 157-159 ◽  
Author(s):  
Ankur Girdhar ◽  
Robert Zaiden

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