Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0206182
Disease: Lymphomatoid Papulosis
Lymphomatoid Papulosis
0.100 Biomarker disease BEFREE Lymphomatoid papulosis (LyP) is a chronic, recurrent lymphoproliferative disorder of the skin that belongs to the group of primary cutaneous CD30-positive T-cell lymphomas. 11168749 2001
CUI: C0206182
Disease: Lymphomatoid Papulosis
Lymphomatoid Papulosis
0.100 Biomarker disease BEFREE Lymphomatoid papulosis (LyP) is defined as a recurrent self-healing papulonodular eruption with the histological features of a (CD30+) cutaneous T-cell lymphoma. 11531801 2001
CUI: C0206182
Disease: Lymphomatoid Papulosis
Lymphomatoid Papulosis
0.100 GeneticVariation disease BEFREE Lymphomatoid papulosis (LyP) is a recurrent, self-healing eruption belonging to the spectrum of cutaneous CD30+lymphoproliferative disorders. 20661014 2010
CUI: C0206182
Disease: Lymphomatoid Papulosis
Lymphomatoid Papulosis
0.100 Biomarker disease BEFREE Lymphomatoid papulosis (LyP) is defined as a chronic recurrent skin disease characterized by waxing and waning papules and nodules with histologic features of a CD30-positive T-cell lymphoma. 22688398 2012
CUI: C0206182
Disease: Lymphomatoid Papulosis
Lymphomatoid Papulosis
0.100 GeneticVariation disease BEFREE Lymphomatoid papulosis (LyP) type E is a recently delineated variant characterized by the occurrence of large necrotic "eschar"-like lesions displaying microscopically angioinvasive and angiodestructive infiltrates composed of CD30 lymphocytes, frequently coexpressing CD8. 28937425 2018
CUI: C0206182
Disease: Lymphomatoid Papulosis
Lymphomatoid Papulosis
0.100 AlteredExpression disease BEFREE Lymphomatoid papulosis type E (LyP) is a recently described subtype of LyP characterized by an angioinvasive infiltrate of atypical lymphocytes expressing CD30. 29067932 2018
CUI: C0206182
Disease: Lymphomatoid Papulosis
Lymphomatoid Papulosis
0.100 GeneticVariation disease BEFREE Lymphomatoid papulosis (LyP) type E is a recently described variant characterized by the occurrence of large necrotic eschar-like lesions displaying microscopically angioinvasive and angiodestructive infiltrates of CD30+ lymphocytes, frequently coexpressing CD8. 30957244 2019
CUI: C0206182
Disease: Lymphomatoid Papulosis
Lymphomatoid Papulosis
0.100 Biomarker disease BEFREE Lymphomatoid papulosis (LyP) is a benign chronic often relapsing skin condition that belongs to the CD30-positive cutaneous lymphoproliferative disorders. 31494989 2020
CUI: C0206182
Disease: Lymphomatoid Papulosis
Lymphomatoid Papulosis
0.100 Biomarker disease BEFREE Lymphomatoid papulosis and cutaneous CD30+ lymphoma. 8806956 1996
CUI: C0206182
Disease: Lymphomatoid Papulosis
Lymphomatoid Papulosis
0.100 Biomarker disease BEFREE CD30+ cutaneous lymphoproliferative disorders include lymphomatoid papulosis (LyP) and anaplastic large cell lymphoma (ALCL). 16412208 2006
CUI: C0206182
Disease: Lymphomatoid Papulosis
Lymphomatoid Papulosis
0.100 Biomarker disease BEFREE CD30-positive primary cutaneous lymphoproliferative disorders include several entities with differing clinical presentation but overlapping histological features, including lymphomatoid papulosis and primary cutaneous anaplastic large cell lymphoma (C-ALCL). 25131361 2015
CUI: C0206182
Disease: Lymphomatoid Papulosis
Lymphomatoid Papulosis
0.100 Biomarker disease BEFREE CD30+ lymphoproliferative disorders (LD) represent a spectrum of entities ranging from self-limited proliferations or cutaneous lesions with favorable prognosis, such as lymphomatoid papulosis and primary cutaneous anaplastic large cell lymphoma (ALCL), to more aggressive malignancies such as systemic ALK-positive and ALK-negative ALCL. 31705818 2019
CUI: C0206182
Disease: Lymphomatoid Papulosis
Lymphomatoid Papulosis
0.100 Biomarker disease BEFREE A skin biopsy revealed a dermal infiltrate of CD4, CD8 and CD30-positive T-cells, consistent with lymphomatoid papulosis. 23713913 2014
CUI: C0206182
Disease: Lymphomatoid Papulosis
Lymphomatoid Papulosis
0.100 Biomarker disease BEFREE Although the papular clinical appearance, lymphocyte atypia, and focal CD30 positivity may resemble LyP, the relatively low number of atypical lymphocytes, low intensity of CD30 staining, and absence of spontaneous resolution help to distinguish PPPD from LyP. 31188140 2020
CUI: C0206182
Disease: Lymphomatoid Papulosis
Lymphomatoid Papulosis
0.100 GeneticVariation disease BEFREE Another photoresponsive CTCL variant is lymphomatoid papulosis (LP), a CD30+ lymphoproliferative disease characterised by chronically recurring papules. 30325389 2018
CUI: C0206182
Disease: Lymphomatoid Papulosis
Lymphomatoid Papulosis
0.100 Biomarker disease BEFREE At present, brentuximab vedotin, an antibody-drug conjugate composed of an anti-cluster of differentiation (CD)-30 antibody covalently linked to monomethyl auristatin E, is approved for the treatment of CD30+ lymphoproliferative disorders [lymphomatoid papulosis (LyP) and primary cutaneous-anaplastic large-cell lymphoma (pc-ALCL)] as well as transformed CD30+ mycosis fungoides (MF). 30430444 2019
CUI: C0206182
Disease: Lymphomatoid Papulosis
Lymphomatoid Papulosis
0.100 AlteredExpression disease BEFREE BIA-ALCL resembles CD30+ cutaneous LPD: ALK-, CD30+ anaplastic cells with an aberrant T cell phenotype; overexpression of oncogenes (JUNB, SATB1, pSTAT3, SOCS3) in lymphomatoid papulosis (LyP); frequent apoptosis; complete spontaneous regression in LyP and partial spontaneous regression in cutaneous ALCL. 31577659 2020
CUI: C0206182
Disease: Lymphomatoid Papulosis
Lymphomatoid Papulosis
0.100 Biomarker disease BEFREE CCR3 was expressed in 73% of cases of CD30+ lymphoproliferative disorders such as lymphomatoid papulosis and anaplastic large cell lymphoma. 31045236 2019
CUI: C0206182
Disease: Lymphomatoid Papulosis
Lymphomatoid Papulosis
0.100 AlteredExpression disease BEFREE CD8-positive lymphomatoid papulosis (type D): Some lesions may lack CD30 expression and overlap histologically with mycosis fungoides. 30520526 2019
CUI: C0206182
Disease: Lymphomatoid Papulosis
Lymphomatoid Papulosis
0.100 Biomarker disease BEFREE Current pathologic criteria cannot reliably distinguish cutaneous anaplastic large cell lymphoma from other CD30-positive T-cell lymphoproliferative disorders (lymphomatoid papulosis, systemic anaplastic large cell lymphoma with skin involvement, and transformed mycosis fungoides). 21169992 2011
CUI: C0206182
Disease: Lymphomatoid Papulosis
Lymphomatoid Papulosis
0.100 Biomarker disease BEFREE Cutaneous CD30+ lymphoproliferative disorders constitute many cutaneous T-cell lymphomas and comprise lymphomatoid papulosis and primary cutaneous anaplastic large cell lymphoma (ALCL).Both have an excellent prognosis. 31466587 2019
CUI: C0206182
Disease: Lymphomatoid Papulosis
Lymphomatoid Papulosis
0.100 Biomarker disease BEFREE Four of these patients subsequently developed MF; (3) Lymphomatoid papulosis (waxing and waning lesions and positivity for CD30) (n=10; M:F=4:6; median age, 41 y; range, 16 to 83 y); (4) MF (clinical features typical of MF) (n=11; M:F=6:5; median age, 17 y; range, 8 to 85 y). 29851705 2018
CUI: C0206182
Disease: Lymphomatoid Papulosis
Lymphomatoid Papulosis
0.100 Biomarker disease BEFREE Immunohistochemical stains for CD8, CD30, CD79 and CLA may be valuable tools in the differential diagnosis between PLEVA and LyP. 11553311 2001
CUI: C0206182
Disease: Lymphomatoid Papulosis
Lymphomatoid Papulosis
0.100 Biomarker disease BEFREE In situ hybridization studies showed positivity of the neoplastic cells for EBER in two of 16 cases of CD30+ ALCL and in none of the cases of LyP. 17076712 2006
CUI: C0206182
Disease: Lymphomatoid Papulosis
Lymphomatoid Papulosis
0.100 Biomarker disease BEFREE In this study, we determined that two allelic forms of the CD30 promoter microsatellite repressive element, designated 30M377 and 30M362, are associated with the development of lymphomatoid papulosis and CD30+ lymphomas in lymphomatoid papulosis patients, respectively. 15894695 2005