scholarly journals Unilateral lung hypoplasia presenting in seventh decade of life: a rare case report

2018 ◽  
Vol 5 (6) ◽  
pp. 1532
Author(s):  
Baishakhi Chandra ◽  
Bhaskar K. ◽  
Paramjyothi G. K.

Pulmonary hypoplasia is a bronchopulmonary foregut anomaly in which gross morphology of the lung is preserved but there is decrease in the number or size of airways, vessels, and alveoli. Unilateral pulmonary hypoplasia is a rare clinical condition and most patients reported in the literature are newborns and infants, but patients may remain asymptomatic until late adolescent or till adulthood 65 years old male with parkinsonism was referred to our department with complaints of recent chest symptoms. Clinical examination revealed loss of lung volume in left hemithorax. CT scan thorax and bronchoscopy confirmed the diagnosis of left sided pulmonary hypoplasia. This case report highlights the possibility of pulmonary hypoplasia as one of the differential diagnoses in adult patients presenting with loss of lung volume and to the best of our knowledge he is the eldest patient so far reported.

2014 ◽  
Vol 24 (2) ◽  
pp. 86-88
Author(s):  
Mohammad Shahidul Islam ◽  
Humayara Tabassum ◽  
Sharah Jahan ◽  
Mohammad Shahin Masud ◽  
Muhammad Al Amin ◽  
...  

Heart failure may present with diverse manifestation. It is far most common cause of bilateral transudative pleural effusion. In very unusual case, it may present with only massive transudative pleural effusion without cardiomegaly and other features of heart failure such as leg odema, tender hepatomegaly or congested liver. We presented a case that present with massive transudative pleural effusion with mediastinal lymphadenopathy evidenced by CT scan of chest and treated successfully with diuretics. DOI: http://dx.doi.org/10.3329/bjmed.v24i2.20223 Bangladesh J Medicine 2013; 24 : 86-88


2013 ◽  
Vol 12 (2) ◽  
pp. 220-223
Author(s):  
Kaleem Ahmad ◽  
Sajid Ansari ◽  
Mukesh Kumar Gupta ◽  
RK Rauniyar ◽  
Mohammed Azfar Siddiqui

Isolated orbital hydatid cyst is a rare manifestation most commonly situated in superomedial and superolateral angles of orbit. We report a case of a 24 years old female with a large retrobulbar orbital hydatid cyst causing proptosis which was not associated with any cyst in other organs. USG and CT scan aids to diagnosis while surgical excision and histopathology confirms the diagnosis. Bangladesh Journal of Medical Science Vol. 12 No. 02 April’13 Page 220-223 DOI: http://dx.doi.org/10.3329/bjms.v12i2.14976


2015 ◽  
Vol 2 (20) ◽  
pp. 3092-3097
Author(s):  
Anita A M ◽  
Dimple Mehrotra ◽  
Pratima S ◽  
Sainath K. Andola ◽  
Megha Kamalapurkar

1970 ◽  
Vol 6 (1) ◽  
pp. 32-33
Author(s):  
MS Rahman ◽  
MA Hossain

This is an interesting and rare case report of right intraorbital cavernous haemangioma near optic nerve of a12 years boy who was hospitalized for right sided uniocular moderate axial proptosis and headache withoutany impairment of vision. Computed Tomographic (CT) scan showed fusiform enlargement of around rightoptic nerve just behind the eye ball. The mass was removed by right fronto-orbito-zygomatotomy incision anddiagnosed post-operatively as intraorbital cavernous haemangioma (CHM).Key words: Intraorbital cavernous haemangioma.DOI: 10.3329/jafmc.v6i1.5990Journal of Armed Forces Medical College, Bangladesh Vol.6(1) 2010 p.32-33


2017 ◽  
Vol 5 (1) ◽  
pp. 262
Author(s):  
Manish Verma ◽  
Shruti Sharma ◽  
Kiran Suthar ◽  
Beena Thada

Meckel gruber syndrome or dysencephalia splanchnocystica, is a rare autosomal recessive disorder caused by failure of mesodermal induction. Worldwide incidence of MGS is 1 per 13,500-140,000 live births. It is characterized by triad of occipital Meningoencephalocele, polycystic kidneys and post-axial polydactyly. Most fetuses affected with this syndrome die before birth due to oligohydramnios, renal failure or pulmonary hypoplasia. We report a rare case of MGS who delivered live at birth with classical features.


2014 ◽  
Author(s):  
Tadeusz Budlewski ◽  
Dorota Szydlarska ◽  
Norbert Szalus ◽  
Jolanta Kijek ◽  
Beata Ewa Chrapko

Author(s):  
Ivana Sagova ◽  
Dušan Pavai ◽  
Matej Stančik ◽  
Helena Urbankova ◽  
Juliana Gregova ◽  
...  

2011 ◽  
Vol 3 (6) ◽  
pp. 405-406
Author(s):  
Dr. Nale Swati S Dr. Nale Swati S ◽  
◽  
Dr.Ghadage Dnyaneshwari P ◽  
Bhore Arvind V

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