منابع مشابه
Cavernous pulmonary telangiectasis.
A cavernous pulmonary telangiectasis is a wide peripheral communication between a dilated, tortuous, thin-walled pulmonary artery and the corresponding pulmonary veins. It is part of a more or less generalized condition of telangiectasia in which small telangiectases are scattered in variable distribution and numbers in the lungs and elsewhere in the body. The striking appearance and obvious cl...
متن کاملA case of multiple pulmonary cavernous hemangioma
A 61-year-old male who originally visited a different hospital, underwent a health checkup in which multiple lung nodules were detected. Multiple well-defined small nodules were observed in both lungs, with lesions reaching the arteries. Metastatic lung cancer, with unknown origin, was suspected. A computed tomography-guided percutaneous lung biopsy was performed; however, a pathological diagno...
متن کاملFatal rupture of pulmonary arteriovenous malformation in hereditary haemorrhagic telangiectasis and severe PAH.
A 29-yr-old patient with hereditary haemorrhagic telangiectasia was referred to the present authors' centre with progressive exertional dyspnoea. Pulmonary arterial hypertension (PAH) was suspected on Doppler echocardiography and confirmed by right heart catheterisation demonstrating severe PAH. Genetic analysis found an activin receptor-like kinase-1 gene missense mutation. Chest radiography a...
متن کاملNeovascular membranes associated with idiopathic juxtafoveolar telangiectasis.
OBJECTIVE To report the visual outcome in patients with a neovascular membrane (NVM) associated with idiopathic juxtafoveolar telangiectasis (IJFT). METHODS We performed a retrospective, noncomparative analysis of 26 eyes of 16 patients with an NVM associated with bilateral IJFT (Gass classification group 2A). Eyes were divided into 2 groups: group WO (n = 11) included eyes with IJFT without ...
متن کاملRecurrent epistaxis secondary to hereditary haemorrhagic telangiectasis.
Familial epistaxis is often encountered by Otolaryngologists. Osier in 1901 described a triad of symptoms consisting of epistaxis, positive family history and multiple telangiectasia. Harrison (1957) regards this phenomena as 'rare' and Mc Caffrey et al. (1977) calls it unusual Multiple Telangiectasia, the cause of which is unknown, has a dominant familial trait. It may be very easily missed wh...
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ژورنال
عنوان ژورنال: Thorax
سال: 1949
ISSN: 0040-6376
DOI: 10.1136/thx.4.3.137