Multifocal Pigment Epithelial Detachments by Reticulum Cell Sarcoma

Gass, J. Donald M.; Sever, Raymond J.; Grizzard, W. Sanderson; Clarkson, John G.; Blumenkranz, Mark S.; Wind, C A; Shugarman, R

doi:10.1097/00006982-198400430-00001

Cited by 92 publications

(36 citation statements)

References 0 publications

Supporting

Mentioning

Contrasting

Unclassified

Order By: Relevance

“…2,6,22,27,42,88,110 They can give rise to a characteristic "leopard skin" pigmentation overlying the mass. 88 There may be isolated subretinal lesions, 134 sometimes with associated exudative retinal detachment. 27 Spontaneous resolution may lead to RPE atrophy with subretinal fibrosis.…”

Section: Ocular Featuresmentioning

confidence: 99%

Primary Intraocular Lymphoma

Seshadri¹,

Jena²,

Tripathy³

2017

Ophthalmology: Current and Future Developments

View full text Add to dashboard Cite

Section: Ocular Featuresmentioning

confidence: 99%

Primary Intraocular Lymphoma

Seshadri¹,

Jena²,

Tripathy³

2017

Ophthalmology: Current and Future Developments

View full text Add to dashboard Cite

“…They may even appear as multiple punctate lesions (Fig 2). [4][5][6][7][8]13,14 Lesions may be infiltrative and involve all layers of the retina, thereby making it difficult to identify precisely which layers of the tissue are involved. The presence of subretinal pigment epithelial masses is felt by some to be pathognomonic of PCNSLO.…”

Section: Posterior Segmentmentioning

confidence: 99%

“…The presence of subretinal pigment epithelial masses is felt by some to be pathognomonic of PCNSLO. 14,15 Retinal hemorrhage is only rarely prominent, and a distinct tumor intrinsic vasculature, as seen in primary choroidal tumors, is typically absent from the lesions. The deep location of the infiltrates can give rise to a nonrhegmatogenous retinal detachment.…”

Section: Posterior Segmentmentioning

confidence: 99%

Intraocular Lymphoma

Bardenstein

1998

Cancer Control

View full text Add to dashboard Cite

Background Primary ocular lymphoma is a distinct subtype of intraocular lymphoma. Its clinical presentation can mimic benign conditions. Diagnosis is often based on obtaining an intraocular biopsy. Optimal management is not yet realized. Methods This report combines the experience of the author with a review of the current literature pertaining to intraocular lymphoma. Results Primary ocular lymphoma, a subtype of primary central nervous system (CNS) lymphoma, has a variable clinical course and frequently mimics benign inflammatory disease. Even when suspected, diagnosis can be elusive. Chemoradiation is the most effective treatment, but significant ocular and cerebral morbidity is associated with its use. Novel treatment regimens may reduce or eliminate side effects while preserving life, vision, and CNS function. Conclusions Primary CNS lymphoma with ocular involvement should be considered in patients with refractory uveitis, yellow-white choroidal masses, and CNS lymphoma. Aggressiveness in making the diagnosis should be tempered by the potential complications of the diagnostic process and advanced by the life-threatening nature of the disease. Treatment should attempt to maximize efficacy while incorporating considerations such as extent of disease and the patient's age, health, and mental state.

show abstract

“…In addition to the differential diagnosis when managing these patients, there are inflammatory choroiditis as sarcoidosis, Vogt-Koyanagi-Harada disease and infectious choroiditis. Various systemic disorders were reported to be associated with PED like malignant 29 http://jors.journals.ekb.eg/ hypertension, leukemia, lymphoma and some renal diseases [9][10][11][12][13] . Whether or not the pathogenesis of PED in all these disorders have a common background is in doubt.…”

Section: Introductionmentioning

confidence: 99%

Retinal Pigment Epithelial Detachment: Three Case Reports

Shouman¹,

Rabie²,

Elhussiny³

2017

Journal of Ophthalmology and Related Sciences

View full text Add to dashboard Cite

Pigment epithelial detachment (PED) is a common entity in age-related macular degeneration and central serous chorioretinopathy. Nevertheless, it can manifest rarely without an obvious causative factor. The authors report 3 cases of PED that were atypical in terms of pattern and age presentation. The second case is associated with sickle cell disease, which has not been reported in literature as far and that could add to our knowledge of this disease entity. Methods: The three cases underwent ophthalmological examination, optical coherence tomography, fundus autoflourescence, fundus fluorescein angiography, full-field electroretinogram and visual evoked potential. Full medical evaluation was done. Results: Bilateral ocular fundus examination showed multiple, rounded lesions scattered all over the fundus in three cases and peripheral retinal pigment epithelial pigmentary changes in the periphery in two cases. Medical evaluation showed one case of sickle cell disease. Conclusion: The number of reports on atypical pigment epithelial detachment and their correlation is limited. In addition its occurrence with sickle cell disease in the second case is a novel correlation which has to be reported and followed-up.

show abstract

Multifocal Pigment Epithelial Detachments by Reticulum Cell Sarcoma

Cited by 92 publications

References 0 publications

Primary Intraocular Lymphoma

Primary Intraocular Lymphoma

Intraocular Lymphoma

Retinal Pigment Epithelial Detachment: Three Case Reports

Contact Info

Product

Resources

About