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Retinoblastoma and beyond: pediatric orbital mass lesions.

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December 2024

Department of Neuroradiology, Istituto Giannina Gaslini, Genoa, Italy.

Various space occupying lesions can arise in the orbit, ranging from developmental anomalies to malignancies, and many of the diseases occurring in children are different from the pathologies in the adult population. As the clinical presentation is frequently nonspecific, radiologic evaluation is essential for lesion detection and characterization as well as patient management. While orbital masses may in some cases involve multiple compartments, a simple compartmental approach is the key for the diagnosis on imaging studies, and MRI is the modality of choice.

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  • The case study describes a patient with chronic myelomonocytic leukemia (CMML) who experienced sudden orbital inflammation, leading to significant eye issues like bulging (proptosis) and increased eye pressure.
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  • The case highlights that CMML, although rare, can cause orbital inflammation and suggests it should be considered in patients with ongoing high levels of monocytes.
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Purpose: To compare the efficacy, safety, and factors influencing the outcomes of trabeculectomy (TE), conventional canaloplasty (cCP), and mitomycin C augmented canaloplasty (mCP) in glaucoma patients.

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Primary Intraocular Lymphoma: Rad-Path and Ophthalmologic Correlation.

AJNR Am J Neuroradiol

September 2024

(1) University of Rochester, School of Medicine and Dentistry, Rochester NY 14620 (D.S), (2) Eastern Virginia Medical School, Norfolk, VA 23507 (J.P), (3) University of Connecticut, School of Medicine, Farmington, CT 06032 (ER), (4) Department of Radiology, Mayo Clinic, Jacksonville, 4500 San Pablo Road, Jacksonville, FL 55902, USA (P.V, A.A, N.S), (5) Department of Radiology, Mayo Clinic, 200 1st Street SW, Rochester, MN 55902, USA (G.B), (6) Department of Pathology, Mayo Clinic, Jacksonville, 4500 San Pablo Road, Jacksonville, FL 55902, USA (S.W).

Primary intraocular lymphoma (PIOL) is a rare form of primary central nervous system lymphoma that poses diagnostic challenges due to its nonspecific clinical features and complex imaging characteristics. This paper presents a focus case and two companion cases, highlighting the complexities in identifying and treating PIOL. In the focus case, A 66-year-old male experienced gradual painless vision loss with choroidal thickening on funduscopic exam and subsequent follow-up MRI.

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