ea0049ep851 | Clinical case reports - Pituitary/Adrenal | ECE2017
Uygur Meliha Melin
, Arikan Izzet Hakki
, Deyneli Oguzhan
, Yavuz Dilek Gogas
Introduction: Pachydermoperiostosis (PDP) is a rare hereditary syndrome with familial and idiopathic forms that is characterized by subperiosteal new bone formation with pain, polyarthritis, cutis vertices grata, seborrhea, hyperhidrosis and digital clubbing. Periostosis and cutaneous thickening along with the absence of any signs of cardiovascular, pulmonary, hepatic, intestinal and mediastinal diseases causing secondary hypertrophic osteoarthropathy suggest PDP. The incidenc...