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Quoted phrase not found in phrase index: "Adenoma of the Retinal Pigment Epithelium"
Page 1
Familial adenomatous polyposis.
Galiatsatos P, Foulkes WD. Galiatsatos P, et al. Am J Gastroenterol. 2006 Feb;101(2):385-98. doi: 10.1111/j.1572-0241.2006.00375.x. Am J Gastroenterol. 2006. PMID: 16454848 Review.
Associated features include upper gastrointestinal tract polyps, congenital hypertrophy of the retinal pigment epithelium, desmoid tumors, and other extracolonic malignancies. ...Attenuated FAP is a phenotypically distinct entity, presenting with fewer than 1 …
Associated features include upper gastrointestinal tract polyps, congenital hypertrophy of the retinal pigment epithelium …
Pigmented and depigmented lesions of the ocular fundus.
Traboulsi EI. Traboulsi EI. Curr Opin Ophthalmol. 2012 Sep;23(5):337-43. doi: 10.1097/ICU.0b013e32835622b0. Curr Opin Ophthalmol. 2012. PMID: 22847029 Review.
PURPOSE OF REVIEW: Pigmented and depigmented ocular fundus lesions (de-POFLs) can be isolated and clinically insignificant, or they may be the hallmark of associated serious systemic disorders such as familial polyposis. The ophthalmologist is often called upon to look for these …
PURPOSE OF REVIEW: Pigmented and depigmented ocular fundus lesions (de-POFLs) can be isolated and clinically insignificant, or they may be t …
Adenoma and Adenocarcinoma of the Retinal Pigment Epithelium: A Review of 51 Consecutive Patients.
Williams BK Jr, Di Nicola M, Acaba-Berrocal LA, Milman T, Mashayekhi A, Lucio-Alvarez JA, Eagle RC Jr, Shields JA, Shields CL. Williams BK Jr, et al. Ophthalmol Retina. 2020 Aug;4(8):829-839. doi: 10.1016/j.oret.2020.03.008. Epub 2020 Mar 18. Ophthalmol Retina. 2020. PMID: 32417354
PURPOSE: To describe the clinical and imaging characteristics, pathologic features, and management options of retinal pigment epithelium (RPE) adenoma/adenocarcinoma. DESIGN: Retrospective case series. ...Increased tumor thickness (P = 0.03) and presen …
PURPOSE: To describe the clinical and imaging characteristics, pathologic features, and management options of retinal pigment …
Segmented retinal layer analysis of chiasmal compressive optic neuropathy in pituitary adenoma patients.
Moon JS, Shin SY. Moon JS, et al. Graefes Arch Clin Exp Ophthalmol. 2020 Feb;258(2):419-425. doi: 10.1007/s00417-019-04560-3. Epub 2019 Dec 18. Graefes Arch Clin Exp Ophthalmol. 2020. PMID: 31853626
AIMS: To evaluate changes in the segmented retinal layers of pituitary adenoma (PA) patients and to identify the relationship between these changes and visual function. ...The PA patients performed a visual field (VF) test before surgery and 1 month after surgery. B …
AIMS: To evaluate changes in the segmented retinal layers of pituitary adenoma (PA) patients and to identify the relationship …
Congenital hypertrophy of the retinal pigment epithelium and familial adenomatous polyposis.
McKay DL. McKay DL. Aust N Z J Ophthalmol. 1993 Feb;21(1):3-6. doi: 10.1111/j.1442-9071.1993.tb00122.x. Aust N Z J Ophthalmol. 1993. PMID: 8388223 Review.
Congenital hypertrophy of the retinal pigment epithelium is a common eye sign in patients with familial adenomatous polyposis (FAP). ...Early detection of disease is desirable, but has in the past been reliant on regular endoscopic examination. The nature of …
Congenital hypertrophy of the retinal pigment epithelium is a common eye sign in patients with familial adenomatous pol …
Fundus lesions of adenomatous polyposis.
Tiret A, Parc C. Tiret A, et al. Curr Opin Ophthalmol. 1999 Jun;10(3):168-72. doi: 10.1097/00055735-199906000-00003. Curr Opin Ophthalmol. 1999. PMID: 10537774 Review.
Congenital hypertrophy of the retinal pigment epithelium (CHRPE) is the most frequent extraintestinal manifestation of familial adenomatous polyposis. ...The combination of genetic analysis and fundus examination offers a 100% diagnostic predictability …
Congenital hypertrophy of the retinal pigment epithelium (CHRPE) is the most frequent extraintestinal manifestation of …
Adenocarcinoma of the retinal pigment epithelium: a diagnostic and therapeutic challenge.
Finger PT, McCormick SA, Davidian M, Walsh JB. Finger PT, et al. Graefes Arch Clin Exp Ophthalmol. 1996 Aug;234 Suppl 1:S22-7. doi: 10.1007/BF02343044. Graefes Arch Clin Exp Ophthalmol. 1996. PMID: 8871146 Review.
BACKGROUND: Adenocarcinoma of the retinal pigment epithelium (RPE) is an uncommon intraocular tumor which has been rarely if ever diagnosed prior to enucleation. ...RESULTS: Two months after radiotherapy the eye developed acute angle-closure glaucoma, seconda …
BACKGROUND: Adenocarcinoma of the retinal pigment epithelium (RPE) is an uncommon intraocular tumor which has been rare …
In patients with a positive family history of familial adenomatous polyposis can the condition be diagnosed from the presence of congenital hypertrophy of the retinal pigment epithelium detected via an eye examination: A systematic review.
Rehan S, Aye K. Rehan S, et al. Clin Exp Ophthalmol. 2020 Jan;48(1):98-116. doi: 10.1111/ceo.13643. Epub 2019 Oct 10. Clin Exp Ophthalmol. 2020. PMID: 31525261
In classic familial adenomatous polyposis (FAP) adenomas become malignant. Congenital hypertrophy of the retinal pigment epithelium (CHRPE) is a retinal pigmented lesion and is the earliest and most common potential extraintestinal manifestation …
In classic familial adenomatous polyposis (FAP) adenomas become malignant. Congenital hypertrophy of the retinal pigment …
Congenital hypertrophy of the retinal pigment epithelium (CHRPE) and familial adenomatous polyposis (FAP).
Rossato M, Rigotti M, Grazia M, Turco AE, Bonomi L. Rossato M, et al. Acta Ophthalmol Scand. 1996 Aug;74(4):338-42. doi: 10.1111/j.1600-0420.1996.tb00704.x. Acta Ophthalmol Scand. 1996. PMID: 8883546
Within the framework of research studies to identify phenotyphic markers for early detection of subjects at risk within a family affected by FAP, attention has recently been paid to congenital hypertrophy of the retinal pigment ephitelium (CHRPE). With the aim of ev …
Within the framework of research studies to identify phenotyphic markers for early detection of subjects at risk within a family affected by …
Neoplasms of the retinal pigment epithelium: the 1998 Albert Ruedemann, Sr, memorial lecture, Part 2.
Shields JA, Shields CL, Gündüz K, Eagle RC Jr. Shields JA, et al. Arch Ophthalmol. 1999 May;117(5):601-8. doi: 10.1001/archopht.117.5.601. Arch Ophthalmol. 1999. PMID: 10326956
BACKGROUND: Neoplasms of the retinal pigment epithelium (RPE) are rare, and little is known about their clinical variations, clinical course, and prognosis. ...Prominent retinal feeder vessels were visualized in 8 patients, 5 of whom had …
BACKGROUND: Neoplasms of the retinal pigment epithelium (RPE) are rare, and little is known about their clinical variat …
43 results