Literature DB >> 22328814

Phenotypic variability of retinocytomas: preregression and postregression growth patterns.

Hana Abouzeid1, Aubin Balmer, Alexandre P Moulin, Asimina Mataftsi, Leonidas Zografos, Francis L Munier.   

Abstract

AIM: To describe the incidence of retinocytomas, their variability at presentation and their growth patterns both before and after regression.
METHODS: Medical notes of the 525 patients of the Jules-Gonin Eye Hospital Retinoblastoma Clinic between 1964 and 2008 were reviewed and the charts of 36 patients with retinocytomas and/or phthisis bulbi were selected.
RESULTS: The proportion of patients with retinocytomas and/or phthisis bulbi was 3.2%. The mean age at diagnosis was 28.7 ± 17 years. Five tumours presented a cystic pattern (5.8%). Evidence of aggressive exophytic disease prior to spontaneous regression was documented in two eyes, and of invasive endophytic disease (regressed vitreous seeding or internal limiting membrane disruption) in three eyes. Twenty patients were followed with a mean follow-up of 44 ± 60 months. Tumour growth was observed in 16% cases, benign cystic enlargement in 4% and malignant transformation in 12%.
CONCLUSION: This large study of retinocytomas substantially expands the published features of retinocytoma by describing the cystic nature of some retinocytomas as well as clinical characteristics of the endophytic and exophytic preregression growth patterns. The authors report two different patterns of reactivation: benign cystic enlargement and malignant transformation with or without cystic growth. Higher than previously reported frequency of growth and possible life-threatening complications impose close lifetime follow-up of retinocytoma patients.

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Year:  2012        PMID: 22328814     DOI: 10.1136/bjophthalmol-2011-300896

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN: 0007-1161            Impact factor:   4.638


  6 in total

1.  Photopsia revealing a retinocytoma.

Authors:  Cristina Santos; Mário Ramalho; Inês Coutinho; Susana Teixeira
Journal:  BMJ Case Rep       Date:  2015-08-04

Review 2.  [Retinoblastoma and retinocytoma (retinoma)].

Authors:  K A Metz; D Westerwick; F Driever; K W Schmid; C H D Le Guin
Journal:  Pathologe       Date:  2017-11       Impact factor: 1.011

3.  Resistant retinoblastoma in a 23-year-old patient.

Authors:  Yacoub A Yousef; Jihad Istetieh; Ibrahim Nawaiseh; Maysa Al-Hussaini; Khalil Alrawashdeh; Imad Jaradat; Iyad Sultan; Mustafa Mehyar
Journal:  Oman J Ophthalmol       Date:  2014-09

4.  Association of bilateral, multiple presumed retinal astrocytic proliferations with combined hamartoma of retina and retinal pigment epithelium in a 9-year-old male child with neurofibromatosis type 2.

Authors:  Pukhraj Rishi; Raj Shri Hirawat; Aditya Verma
Journal:  Indian J Ophthalmol       Date:  2016-11       Impact factor: 1.848

5.  Unilateral retinocytoma associated with a variant in the RB1 gene.

Authors:  Shijing Wu; Xuan Zou; Zixi Sun; Tian Zhu; Xing Wei; Ruifang Sui
Journal:  Mol Genet Genomic Med       Date:  2020-01-29       Impact factor: 2.183

6.  Optical coherence tomography (OCT) to image active and inactive retinoblastomas as well as retinomas.

Authors:  Oleg Nadiarnykh; Nuray A McNeill-Badalova; Marie-Claire Gaillard; Machteld I Bosscha; Armida W M Fabius; Frank D Verbraak; Francis L Munier; Johannes F de Boer; Annette C Moll
Journal:  Acta Ophthalmol       Date:  2019-08-26       Impact factor: 3.761

  6 in total

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