Pancreatic lipomatosis in cystic fibrosis: Rare manifestation of an uncommon disease

Intractable Rare Dis Res. 2017 May;6(2):150-151. doi: 10.5582/irdr.2017.01008.

Abstract

Cystic fibrosis is deemed to be uncommon in India. The presentation is usually in the childhood although more cases are now being recognized in adolescence and adulthood. We report a case of an adolescent male who had been treated for recurrent pulmonary infections and received anti-tubercular therapy for a possible diagnosis of sputum negative pulmonary tuberculosis and was evaluated for steatorrhea. The presence of pancreatic exocrine insufficiency along with pancreatic lipomatosis suggested the diagnosis of cystic fibrosis.

Keywords: Cystic fibrosis; bronchiectasis; endoscopic ultrasound; pancreatic exocrine insufficiency; steatorrhea.