Purtscher-like retinopathy associated with dermatomyositis
© Yan and Shen; licensee BioMed Central Ltd. 2013
Received: 23 February 2013
Accepted: 12 July 2013
Published: 24 July 2013
To report a rare case of bilateral Purtscher-like retinopathy in a Chinese female patient with dermatomyositis.
An 18-year-old woman with lower extremity muscle weakness was admitted due to decreased vision of both eyes for two weeks. Ophthalmic examination revealed violaceous eruption on eyelids with swelling. Ocular fundus examination revealed multiple cotton wool spots and Purtscher flecken, and intra-retinal haemorrhages with pseudo-cherry red spot. The erythrocyte sedimentation rate, C-reactive protein, lactate dehydrogenase and creatine kinase was measured and found to be increased. A diagnosis of Purtscher-like retinopathy associated with dermatomyositis was made and the patient was treated with corticosteroids.
Although dermatomyositis is a rare cause of Purtscher-like retinopathy, it is important to keep in mind that systemic associations such as dermatomyositis should be ruled out in such patients.
Dermatomyositis is one of the idiopathic inflammatory myopathies. It is characterized clinically by progressive symmetrical proximal muscle weakness, a characteristic heliotropic rash on the eyelids and Gottron papules over bony prominences . Retinopathy associated with dermatomyositis is rare and was first described by Bruce in 1938 . Since then a few case reports have reported it in both adults and children . The most predominant ocular lesion is a heliotropic rash. The characteristic retinal lesions include retinal hemorrhages and cotton-wool spots. Purtscher-like retinopathy is seen in patients with several kinds of connective tissue disorders, particularly systemic lupus erythematosis . Acute fundus abnormalities in Purtscher-like retinopathy include Purtscher flecken, cotton-wool spots, retinal hemorrhage, and optic disc swelling . To our knowledge, few reports have described Purtscher-like retinopathy associated with dermatomyositis . Herein we report a rare case of bilateral Purtscher-like retinopathy in a Chinese female patient with dermatomyositis.
Purtscher's retinopathy was first described in 1910 by Otmar Purtscher, in a patient with severe head trauma . Since then, a similar retinal appearance has also been described in a variety of conditions including acute pancreatitis, crush injury, long bone fracture, orthopaedic surgery, childbirth, and connective tissue disorders . This case was characterized by the occurrence of Purtscher-like retinopathy as an early complication of dermatomyositis. The diagnosis of dermatomyositis was according to the criteria of Bohan and Peter .
The pathognomonic Purtscher flecken occur in only 50% of cases , and they were poorly recognized and documented in many patients . These polygonal areas of retinal whitening occur in the inner retina, between the affected retinal arterioles and venules and have a characteristic clear zone, which described as an average of 50 μm unaffected zone on either side of the retinal arteries and precapillary arterioles . Large emboli produce the confluent retinal whitening, which can be seen in branch retinal arterial obstruction, whereas distal retinal capillaries occlusion by small emboli forms the cotton-wool spots. Purtscher flecken results from occlusion of precapillary arterioles by intermediate-sized emboli.
Several kinds of emboli have been reported to participate in the pathogenesis of Purtscher’s retinopathy and Purtscher-like retinopathy, such as air, fat, leukocyte aggregates, fibrin, platelets and complement activation . Brigitte et al. have described Purtscher-like retinopathy in a 7-year-old boy with severe juvenile dermatomyositis, suggesting that retinal vascular involvement might result from thrombotic thrombocytopenic purpura (TTP) rather than as a complication of juvenile dermatomyositis . However, dermatomyositis seems to have been the cause of our patient’s retinopathy because she didn’t meet the criteria for TTP. Dermatomyositis is characterized pathologically by varying degrees of perifascicular atrophy, vasculopathy, and perivascular inflammation . Obviously some factors such as leukocytes and inflammation may play an important role in our patient. Leukocyte aggregates induced by complement activation, which occur in connective tissue disorders, are usually up to 50 μm in diameter and may occlude the 45 μm diameter precapillary arterioles in the human retina . Vasculitis due to the capillary endothelial damage by inflammatory factors may also contribute to the pathogenesis.
At present no treatment has been proven to be definitely effective . Isolated case reports suggest that treatment of Purtscher's retinopathy with high dose intravenous steroids may be beneficial . While in a prospective observational study, spontaneous visual recovery of at least 2 Snellen lines is seen in half of the cases . The poor outcome of visual acuity may be associated with the optic disc or macular involvement and the extent of retinal vascular occlusion .
In summary, Purtscher-like retinopathy rarely presents as an early manifestation of dermatomyositis. To avoid missing the diagnosis, attention should be paid to identify the characteristic Purtscher flecken. A patient with Purtscher-like retinopathy should be carefully examined and have lab work performed to rule out dermatomyositis. Treatment with systemic steroids may improve visual outcome in some patients, but the visual prognosis is also influenced by the amount of emboli as well as its location and stability.
Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
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