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PedAM

Pediatric Disease Annotations & Medicines




Disease lymphoma
Phenotype C0281658|primary intraocular lymphoma
Sentences 8
PubMedID- 20463797 A primary intraocular lymphoma (piol) is a subtype of primary non-hodgkin’s lymphomas of the central nervous system in which the retina, vitreous, and/or optic nerve head may be involved.1–3 patients with a piol typically present with a form of uveitis and vitritis that is unresponsive to corticosteroid therapy, thus the so-called uveitis masquerade syndrome.
PubMedID- 24612100 Primary intraocular lymphoma (piol) is a lymphoma whose lesion is located in the eye ball, including the vitreous body, the retina, the choroid, the iris, and the ciliary muscle.
PubMedID- 23524026 The most common primary tumors of the eye are uveal melanoma and primary intraocular lymphoma in adults and retinoblastoma in children[2,3].
PubMedID- 23405064 Primary intraocular lymphoma (piol), also called primary vitreoretinal lymphomas [1], is a subset of primary central nervous system lymphoma (pcnsl) that initially presents in the eye, with or without simultaneous cns involvement [2], [3].
PubMedID- 26483672 Primary intraocular lymphoma (piol) may develop in patients receiving mtx and tnf inhibitor treatment.
PubMedID- 22454757 Primary intraocular lymphoma should be considered in young adults suffering from chronic recalcitrant panuveitis.
PubMedID- 23589676 She was diagnosed with primary intraocular lymphoma in both eyes and received intravitreal and intraspinal methotrexate therapy.
PubMedID- 21180448 Cassoux et al.2 reported 42 cases and hormigo et al.3 reported 31 cases of primary intraocular lymphoma in their respective study cohorts.

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