Literature DB >> 2343189

Combined hamartomas of the retinal pigment epithelium and retina.

M L Palmer1, M D Carney, J L Combs.   

Abstract

Combined hamartomas of the retinal pigment epithelium (RPE) and retina are rare, benign lesions usually occurring in individuals with no underlying systemic abnormalities. The authors report two cases of combined hamartomas of the RPE and retina. In one case, combined macular hamartomas of the RPE and retina were present in a 5-month-old infant. This is the earliest reported case of bilateral macular involvement. In both patients, multiple cafe-au-lait spots were present, and the diagnosis of neurofibromatosis was considered. The authors suggest that combined hamartomas of the RPE and retina are congenital lesions and may be one of the ophthalmic manifestations of the phakomatoses.

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Year:  1990        PMID: 2343189

Source DB:  PubMed          Journal:  Retina        ISSN: 0275-004X            Impact factor:   4.256


  5 in total

Review 1.  Clinical and genetic patterns of neurofibromatosis 1 and 2.

Authors:  N K Ragge
Journal:  Br J Ophthalmol       Date:  1993-10       Impact factor: 4.638

2.  Retinal changes associated with neurofibromatosis 2.

Authors:  S M Meyers; F A Gutman; L D Kaye; A D Rothner
Journal:  Trans Am Ophthalmol Soc       Date:  1995

3.  Combined hamartoma of the retina and retinal pigment epithelium associated with neurofibromatosis type-1.

Authors:  R N Vianna; D F Pacheco; M M Vasconcelos; J J de Laey
Journal:  Int Ophthalmol       Date:  2001       Impact factor: 2.031

4.  Familial bilateral combined hamartoma of retina and retinal pigment epithelium associated with neurofibromatosis 1.

Authors:  Sanaa A Yassin; Elham R Al-Tamimi
Journal:  Saudi J Ophthalmol       Date:  2012-03-19

5.  Indocyanine green angiographic findings of obscure choroidal abnormalities in neurofibromatosis.

Authors:  Yong Soo Byun; Young Hoon Park
Journal:  Korean J Ophthalmol       Date:  2012-05-22
  5 in total

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