2012
DOI: 10.1016/j.adengl.2012.04.005
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Follicular Lymphoma With Paraneoplastic Autoimmune Multiorgan Syndrome

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Cited by 2 publications
(2 citation statements)
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“…From the literature search, we included an additional 124 articles, reporting 208 patients with PAMS published between January 1, 1996, and August 1, 2012 . A single article reporting patients from our institution was excluded from analysis to avoid duplicate reporting .…”
Section: Resultsmentioning
confidence: 99%
“…From the literature search, we included an additional 124 articles, reporting 208 patients with PAMS published between January 1, 1996, and August 1, 2012 . A single article reporting patients from our institution was excluded from analysis to avoid duplicate reporting .…”
Section: Resultsmentioning
confidence: 99%
“…1 [2], PNP has now been recognized as a multisystem disorder and renamed as paraneoplastic autoimmune Multiorgan syndrome [3]. Although virtually any mucosa may be involved, painful oral erosions are the earliest and a hallmark feature and its absence argues against a diagnosis of PNP [4]. Polymorphous cutaneous lesions follows mucosal involvement (although isolated mucosal disease has been described) and may resemble PV, Pemphigus foliaceus (PF), Bullous Pemphigoid (BP), lichen planus (LP), Steven-Johnson's syndrome (SJS), Graft-versus-host disease (GVHD) and herpes stomatitis [1,5].…”
mentioning
confidence: 99%