%0 Journal Article
%T Fanconi anaemia with bilateral diffuse pulmonary arterio venous fistulae: a case report
%A Lasitha Samarakoon
%A Nuwan Ranawaka
%A Chaturaka Rodrigo
%A Godwin R Constantine
%A Lalindra Goonarathne
%J BMC Blood Disorders
%D 2012
%I BioMed Central
%R 10.1186/1471-2326-12-1
%X A 16 year old Sri Lankan boy, with a cytogenetically confirmed Fanconi anaemia was admitted to University Medical Unit, National Hospital of Sri Lanka for further assessment and treatment. Both central and peripheral cyanosis plus clubbing were noted on examination. The peripheral saturation was persistently low on room air and did not improve with supplementary Oxygen. Contrast echocardiography failed to demonstrate an intra cardiac shunt but showed early crossover of contrast, suggesting the possibility of pulmonary arterio-venous fistulae. Computed tomography pulmonary angiogram was inconclusive. Subsequent right heart catheterisation revealed bilateral diffuse arterio-venous fistulae not amenable for device closure or surgical intervention.To our knowledge, this is the second reported patient with diffuse pulmonary arterio-venous fistulae associated with Fanconi anaemia. We report this case to create awareness among clinicians regarding this elusive association. We recommend screening patients with Fanconi anaemia using contrast echocardiography at the time of assessment with transthoracic echocardiogram. Though universal screening may be impossible given the cost constraints, such screening should at least be performed in patients with clinical evidence of desaturation or when a therapeutic option such as haematopoietic stem cell transplantation is considered. Treatment of pulmonary arteriovenous fistulae would improve patient outcome as desaturation by shunting worsens the anaemic symptoms by reducing the oxygen carrying capacity of blood.Fanconi anaemia (FA) is commonly inherited as an autosomal recessive trait but rarely can be an X-linked recessive disorder [1]. It is well known that FA patients display progressive bone marrow failure and an increased predisposition to malignancy [2]. They may also have one or more somatic abnormalities including dermatological (e.g. cafe'au lait spots), skeletal (e.g. hypoplastic thumbs, scoliosis), genitourinary (e.g. hor
%K Fanconi anaemia
%K Associations
%K Pulmonary arterio venous fistulae
%K Transthoracic echocardiogram
%K Contrast echocardiography
%K Right heart catheterisation
%U http://www.biomedcentral.com/1471-2326/12/1