Journal of Medical Society

CASE REPORT
Year
: 2014  |  Volume : 28  |  Issue : 3  |  Page : 190--192

Congenital cystic malformation masquerading as a lung abscess in an adult: A report of a rare case


Sandhya V Poflee, Asha Zutshi, Pradnya S Bhadarge, Alok C Shrivastava 
 Department of Pathology, Indira Gandhi Government Medical College, Nagpur, Maharashtra, India

Correspondence Address:
Sandhya V Poflee
Department of Pathology, Indira Gandhi Government Medical college, Nagpur, Maharashtra
India

A 19 year-old male was getting admitted repeatedly, for complaints of cough with expectoration and fever since last 10 years. On the basis of clinical examination and radiological investigations lung abscess of right lower lobe was suspected. Non-functioning right lung lobe of the patient was removed surgically and sent for histopathological examination. Histopathology showed it to be cystic adenomatoid malformation of lung type I, with no evidence of any other specific disease. Congenital cystic adenomatoid malformation (CCAM) is an anomaly of lung development characterized by proliferation of abnormal bronchiolar structures of varying sizes and distribution. It is usually diagnosed in infancy. It is rare in adults. Awareness about this entity help clinicians while making differential diagnosis of recurrent pulmonary infection limited to one lobe. Morphological identification of CCAM is important as Type I CCAM; the most frequent subtype is associated with an increased incidence of malignant transformation.


How to cite this article:
Poflee SV, Zutshi A, Bhadarge PS, Shrivastava AC. Congenital cystic malformation masquerading as a lung abscess in an adult: A report of a rare case.J Med Soc 2014;28:190-192


How to cite this URL:
Poflee SV, Zutshi A, Bhadarge PS, Shrivastava AC. Congenital cystic malformation masquerading as a lung abscess in an adult: A report of a rare case. J Med Soc [serial online] 2014 [cited 2020 Dec 4 ];28:190-192
Available from: https://www.jmedsoc.org/article.asp?issn=0972-4958;year=2014;volume=28;issue=3;spage=190;epage=192;aulast=Poflee;type=0