Diffuse Anterior Retinoblastoma with Sarcoidosis-Like Nodule

Background: Retinoblastomas account for 4% of malignancies in children, 1-2% of which are diffuse infiltrating retinoblastomas. Diffuse anterior retinoblastoma is rare and does not involve the retina. Here, we report on a diffuse anterior retinoblastoma with large sarcoidosis-like nodules on the iri...

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Main Authors: Koji Kitazawa, Kenji Nagata, Yukito Yamanaka, Yasumichi Kuwahara, Tomoko Iehara, Shigeru Kinoshita, Chie Sotozono
Format: Article
Language:English
Published: Karger Publishers 2015-12-01
Series:Case Reports in Ophthalmology
Subjects:
Online Access:http://www.karger.com/Article/FullText/442744
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spelling doaj-66972db12c214d8cad492f0eebe29a1b2020-11-24T23:41:35ZengKarger PublishersCase Reports in Ophthalmology1663-26992015-12-016344344710.1159/000442744442744Diffuse Anterior Retinoblastoma with Sarcoidosis-Like NoduleKoji KitazawaKenji NagataYukito YamanakaYasumichi KuwaharaTomoko IeharaShigeru KinoshitaChie SotozonoBackground: Retinoblastomas account for 4% of malignancies in children, 1-2% of which are diffuse infiltrating retinoblastomas. Diffuse anterior retinoblastoma is rare and does not involve the retina. Here, we report on a diffuse anterior retinoblastoma with large sarcoidosis-like nodules on the iris that were responsive to anti-inflammatory therapy. Case: We present a 6-year-old girl who had anterior uveitis with white nodules on the iris and posterior surface of the cornea in her right eye. The nodules initially responded well to anti-inflammatory treatment. However, anterior segment optical coherence tomography (AS-OCT) showed that the nodules gradually grew, shrinking the iris. We then collected the aqueous humor for diagnosis. A biopsy revealed clusters of small cells with a high nuclear-to-cytoplasm ratio with partial rosette formation. Therefore, we diagnosed diffuse anterior retinoblastoma without retinal involvement and performed enucleation of the right eye. The histopathology demonstrated undifferentiated cells similar to those seen on the biopsy, and tumor cells invaded the iris stroma, posterior surface of the cornea, ciliary body, and sclera. After the enucleation, she underwent chemotherapy and remains alive. Conclusion: A differential diagnosis of retinoblastoma should be considered when white nodules refractory to anti-inflammatory therapy occur in the eye, even in the absence of obvious retinal masses. AS-OCT findings are useful in assessing retinoblastoma.http://www.karger.com/Article/FullText/442744ChemotherapySarcoidosisDiffuse infiltrating retinoblastomaAnterior segment optical coherence tomographyEnucleationRetinoblastomaDiffuse anterior retinoblastoma
collection DOAJ
language English
format Article
sources DOAJ
author Koji Kitazawa
Kenji Nagata
Yukito Yamanaka
Yasumichi Kuwahara
Tomoko Iehara
Shigeru Kinoshita
Chie Sotozono
spellingShingle Koji Kitazawa
Kenji Nagata
Yukito Yamanaka
Yasumichi Kuwahara
Tomoko Iehara
Shigeru Kinoshita
Chie Sotozono
Diffuse Anterior Retinoblastoma with Sarcoidosis-Like Nodule
Case Reports in Ophthalmology
Chemotherapy
Sarcoidosis
Diffuse infiltrating retinoblastoma
Anterior segment optical coherence tomography
Enucleation
Retinoblastoma
Diffuse anterior retinoblastoma
author_facet Koji Kitazawa
Kenji Nagata
Yukito Yamanaka
Yasumichi Kuwahara
Tomoko Iehara
Shigeru Kinoshita
Chie Sotozono
author_sort Koji Kitazawa
title Diffuse Anterior Retinoblastoma with Sarcoidosis-Like Nodule
title_short Diffuse Anterior Retinoblastoma with Sarcoidosis-Like Nodule
title_full Diffuse Anterior Retinoblastoma with Sarcoidosis-Like Nodule
title_fullStr Diffuse Anterior Retinoblastoma with Sarcoidosis-Like Nodule
title_full_unstemmed Diffuse Anterior Retinoblastoma with Sarcoidosis-Like Nodule
title_sort diffuse anterior retinoblastoma with sarcoidosis-like nodule
publisher Karger Publishers
series Case Reports in Ophthalmology
issn 1663-2699
publishDate 2015-12-01
description Background: Retinoblastomas account for 4% of malignancies in children, 1-2% of which are diffuse infiltrating retinoblastomas. Diffuse anterior retinoblastoma is rare and does not involve the retina. Here, we report on a diffuse anterior retinoblastoma with large sarcoidosis-like nodules on the iris that were responsive to anti-inflammatory therapy. Case: We present a 6-year-old girl who had anterior uveitis with white nodules on the iris and posterior surface of the cornea in her right eye. The nodules initially responded well to anti-inflammatory treatment. However, anterior segment optical coherence tomography (AS-OCT) showed that the nodules gradually grew, shrinking the iris. We then collected the aqueous humor for diagnosis. A biopsy revealed clusters of small cells with a high nuclear-to-cytoplasm ratio with partial rosette formation. Therefore, we diagnosed diffuse anterior retinoblastoma without retinal involvement and performed enucleation of the right eye. The histopathology demonstrated undifferentiated cells similar to those seen on the biopsy, and tumor cells invaded the iris stroma, posterior surface of the cornea, ciliary body, and sclera. After the enucleation, she underwent chemotherapy and remains alive. Conclusion: A differential diagnosis of retinoblastoma should be considered when white nodules refractory to anti-inflammatory therapy occur in the eye, even in the absence of obvious retinal masses. AS-OCT findings are useful in assessing retinoblastoma.
topic Chemotherapy
Sarcoidosis
Diffuse infiltrating retinoblastoma
Anterior segment optical coherence tomography
Enucleation
Retinoblastoma
Diffuse anterior retinoblastoma
url http://www.karger.com/Article/FullText/442744
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