Vitreoretinal lymphomas misdiagnosed as uveitis: Lessons learned from a case series
Autor: | Matteo Belpoliti, Alfonso Iovieno, Marco Coassin, Andrea Fanti, Luca Cimino, Chi-Chao Chan, Luigi Fontana, Sylvia Marchi |
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Předmět: |
0301 basic medicine
Male medicine.medical_treatment intraocular inflammation Vitrectomy Subretinal infiltrates 0302 clinical medicine lcsh:Ophthalmology Intraocular Lymphoma Pathognomonic Sampling (medicine) Aged 80 and over vitreoretinal lymphoma Middle Aged Original Article Female Intraocular lymphoma Diagnostic vitrectomy Intraocular inflammation Uveitis Vitreoretinal lymphoma Tomography Optical Coherence medicine.medical_specialty Retinal Neoplasm Retinal Neoplasms Enzyme-Linked Immunosorbent Assay 03 medical and health sciences medicine Biomarkers Tumor Humans Diagnostic Errors Aged Retrospective Studies business.industry Interleukins Retrospective cohort study medicine.disease Occult Dermatology Surgery Vitreous Body Ophthalmology 030104 developmental biology subretinal infiltrates lcsh:RE1-994 030221 ophthalmology & optometry business Follow-Up Studies |
Zdroj: | Europe PubMed Central Indian Journal of Ophthalmology Indian Journal of Ophthalmology, Vol 64, Iss 5, Pp 369-375 (2016) |
Popis: | Purpose: To present challenging cases of vitreoretinal lymphoma (VRL) that was misdiagnosed as uveitis because of the apparent intraocular inflammation. At the light of the new classification of intraocular lymphomas, we detail the characteristics that masqueraded the tumors and the clinical aspects that guided us to the correct diagnosis. Materials and Methods: We retrospectively reviewed the patients referred to our uveitis service between January 2006 and December 2014. Results: Seven patients referred with a presumptive diagnosis of idiopathic uveitis received a final diagnosis of VRL. The median time between the onset of symptoms and definitive diagnosis was 25 months for these complex cases. The median time from presentation at our clinic to final diagnosis was 1 month. The described clinical features including dense vitreous cells and subretinal infiltrates were characteristic and tend to be present in all these chronically ill patients. Vitreous samples were collected, and all demonstrated the pathognomonic tumor cells, the specific immunoglobulin heavy chain gene rearrangements, and an interleukin (IL)-10 to IL-6 ratio >1. Conclusion: VRLs are severe diseases with a poor prognosis that may be misdiagnosed as idiopathic inflammatory conditions of the eye. Treatment with steroids may occult the tumors and delay the correct diagnosis. Appropriate evaluation may prompt to a timely vitreous sampling and therefore to a faster diagnosis in these peculiar cases where the correct diagnosis was delayed by several months. |
Databáze: | OpenAIRE |
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