학술논문

Deoxyguanosine kinase deficiency and recurrent spontaneous pneumothorax: a case report
Document Type
article
Source
Journal of Medical Case Reports, Vol 17, Iss 1, Pp 1-4 (2023)
Subject
Deoxyguanosine kinase deficiency
Mitochondrial DNA depletion syndrome
Mitochondriopathy
Amyotrophy
Recurrent spontaneous pneumothorax
Case report
Medicine
Language
English
ISSN
1752-1947
Abstract
Abstract Background Deoxyguanosine kinase deficiency is mainly manifested by hepatic and neurological damage, hence it belongs to the hepatocerebral form of mitochondrial deoxyribonucleic acid depletion syndrome. The association between deoxyguanosine kinase deficiency and recurrent spontaneous pneumothorax has not currently been reported. Case presentation A 12-year-old Russian boy with deoxyguanosine kinase deficiency, a recipient of a liver transplant with amyotrophy secondary to his mitochondriopathy, presented with recurrent spontaneous bilateral pneumothorax refractory to drainage and surgery. Conclusion To our knowledge, this is the first documented case of deoxyguanosine kinase deficiency associated with recurrent spontaneous pneumothorax, which could be considered a late complication of deoxyguanosine kinase deficiency. At this point, this is only an association and further studies and research need to be performed to help confirm the pathogenesis of this association.