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1.
Yonsei Medical Journal ; : 799-802, 2016.
Article in English | WPRIM | ID: wpr-205732

ABSTRACT

A 20-year-old female had undergone definitive surgical repair for pulmonary atresia with intact ventricular septum soon after birth. She was referred to our institution with the chief complaint of clubbing fingers. A thorough examination revealed platypnea-orthodeoxia syndrome due to an interatrial right-to-left shunt through a secundum atrial septal defect. Percutaneous closure with an Amplatzer Septal Occluder resulted in resolution of the syndrome.


Subject(s)
Female , Humans , Dyspnea/diagnosis , Heart Defects, Congenital/complications , Heart Septal Defects, Atrial/complications , Hypoxia , Pulmonary Atresia/complications , Septal Occluder Device , Syndrome , Treatment Outcome
2.
Chinese Journal of Rheumatology ; (12): 263-265,插2, 2008.
Article in Chinese | WPRIM | ID: wpr-592343

ABSTRACT

Objective To improve the understanding and diagnosis of primary hypertrophic os-teoathropathy(PHO).Methods A case of PHO was reported.The clinical data and the process of the diagno-sis and treatment was analyzed retrospectively,and the related literature were reviewed.Results The patient was a young man without family history of PHO.He had symptoms since age 16.He had clubbing fingers and toes,hypertrophic skin,joint swelling,hyperhidrosis and radiographic evidence of periostitis.Thus the disease was diagnosed as PHO.The patient was treated with NSAIDs and the symptoms relieved very quickly.Conclusion Radiographic examination should be taken in time when young males have the general characters of clubbing fingers and toes,hypertrophic skin changes.If the periostitis presents,the final diagnosis of PHO can be confirmed.

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