Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0024314
Disease: Lymphoproliferative Disorders
Lymphoproliferative Disorders
0.100 AlteredExpression group BEFREE Th2 cytokine mRNA expression in primary cutaneous CD30-positive lymphoproliferative disorders: successful treatment with recombinant interferon-gamma. 8941669 1996
CUI: C0024314
Disease: Lymphoproliferative Disorders
Lymphoproliferative Disorders
0.100 Biomarker group BEFREE Our results support the hypothesis that (1) primary cutaneous CD30+ LPDs (including LyP) and primary nodal ALCL are distinct diseases that differ in clinical behavior and pathogenesis and (2) differential expression of t(2;5) can help to distinguish between primary cutaneous CD30+ LPDs and ALCL of nodal origin. 8605362 1996
CUI: C0024314
Disease: Lymphoproliferative Disorders
Lymphoproliferative Disorders
0.100 Biomarker group BEFREE Several primary cutaneous lymphoproliferative disorders and Hodgkin's disease are also known to contain CD30+ large lymphoid cells. 8781433 1996
CUI: C0024314
Disease: Lymphoproliferative Disorders
Lymphoproliferative Disorders
0.100 Biomarker group BEFREE This points to a molecular aetiology of primary cutaneous ALC lymphomas and LyP distinct from that of extracutaneous CD30+ lymphoproliferative disease. 9415224 1997
CUI: C0024314
Disease: Lymphoproliferative Disorders
Lymphoproliferative Disorders
0.100 Biomarker group BEFREE Most primary cutaneous CD30-positive lymphoproliferative disorders have a CD4-positive cytotoxic T-cell phenotype. 9347791 1997
CUI: C0024314
Disease: Lymphoproliferative Disorders
Lymphoproliferative Disorders
0.100 Biomarker group BEFREE The t(2;5)-associated p80 NPM/ALK fusion protein in nodal and cutaneous CD30+ lymphoproliferative disorders. 9449486 1997
CUI: C0024314
Disease: Lymphoproliferative Disorders
Lymphoproliferative Disorders
0.100 Biomarker group BEFREE Additional studies will be needed to determine if t(2;5) status has any clinical significance for patients with CD30+ primary cutaneous lymphoproliferative disorders. 9638979 1998
CUI: C0024314
Disease: Lymphoproliferative Disorders
Lymphoproliferative Disorders
0.100 Biomarker group BEFREE In contrast, primary cutaneous CD30+ lymphoproliferative disorders form a heterogeneous spectrum including anaplastic large cell lymphomas, the majority of which display a good prognosis. 10955685 2000
CUI: C0024314
Disease: Lymphoproliferative Disorders
Lymphoproliferative Disorders
0.100 Biomarker group BEFREE The CD30 (Ki-1)-positive lymphoproliferative disorders show a non-epidermotropic infiltrate of large-sized pleomorphic T cells, being extremely rare those that develop from B cells. 11972717 2002
CUI: C0024314
Disease: Lymphoproliferative Disorders
Lymphoproliferative Disorders
0.100 Biomarker group BEFREE Seven of 12 (58%) cutaneous CD30-positive lymphoproliferative disorders were also ZAP-70-positive. 15133473 2004
CUI: C0024314
Disease: Lymphoproliferative Disorders
Lymphoproliferative Disorders
0.100 Biomarker group BEFREE The lesions in these patients seem to be the oral counterpart of the spectrum of primary cutaneous CD30+ lymphoproliferative disorders and should be recognized as such to avoid a diagnosis of large T-cell lymphoma and possible consequent overtreatment. 14750239 2004
CUI: C0024314
Disease: Lymphoproliferative Disorders
Lymphoproliferative Disorders
0.100 Biomarker group BEFREE In particular, differences in the classification of cutaneous T-cell lymphomas other than mycosis fungoides, Sezary syndrome, and the group of primary cutaneous CD30+ lymphoproliferative disorders and the classification and terminology of different types of cutaneous B-cell lymphomas have resulted in considerable debate and confusion. 15692063 2005
CUI: C0024314
Disease: Lymphoproliferative Disorders
Lymphoproliferative Disorders
0.100 Biomarker group BEFREE These findings suggest that allele-specific differences in the control of CD30 transcription may determine the pathogenesis of the spectrum of CD30+ cutaneous lymphoproliferative disorders. 15894695 2005
CUI: C0024314
Disease: Lymphoproliferative Disorders
Lymphoproliferative Disorders
0.100 Biomarker group BEFREE Detection of clonal rearrangement of T-cell receptor genes in the diagnosis of primary cutaneous CD30 lymphoproliferative disorders. 17083688 2006
CUI: C0024314
Disease: Lymphoproliferative Disorders
Lymphoproliferative Disorders
0.100 Biomarker group BEFREE CD30+ cutaneous lymphoproliferative disorders include lymphomatoid papulosis (LyP) and anaplastic large cell lymphoma (ALCL). 16412208 2006
CUI: C0024314
Disease: Lymphoproliferative Disorders
Lymphoproliferative Disorders
0.100 Biomarker group BEFREE The current clinicopathologic classification of CD30+ cutaneous lymphoproliferative disorders is insufficient. 17387297 2007
CUI: C0024314
Disease: Lymphoproliferative Disorders
Lymphoproliferative Disorders
0.100 Biomarker group BEFREE A few recent case reports have demonstrated molecular evidence of T-cell clonality in TUGSE and CD30 immunoreactivity in the large atypical mononuclear cells, raising the possibility that a TUGSE subset may represent the oral counterpart of primary cutaneous CD30+ T-cell lymphoproliferative disorders. 19846813 2009
CUI: C0024314
Disease: Lymphoproliferative Disorders
Lymphoproliferative Disorders
0.100 Biomarker group BEFREE Systemic anaplastic large cell lymphoma (ALCL) involving the skin should be differentiated from primary cutaneous CD30-positive T-cell lymphoproliferative disorders. 19091487 2009
CUI: C0024314
Disease: Lymphoproliferative Disorders
Lymphoproliferative Disorders
0.100 Biomarker group BEFREE Lymphomatoid papulosis (LyP) is a recurrent, self-healing eruption belonging to the spectrum of cutaneous CD30+lymphoproliferative disorders. 20661014 2010
CUI: C0024314
Disease: Lymphoproliferative Disorders
Lymphoproliferative Disorders
0.100 Biomarker group 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: C0024314
Disease: Lymphoproliferative Disorders
Lymphoproliferative Disorders
0.100 Biomarker group BEFREE Anaplastic large cell cutaneous lymphomas are clinically and pathologically heterogeneous, CD30 + (Ki-1) lymphoproliferative disorders. 22565437 2012
CUI: C0024314
Disease: Lymphoproliferative Disorders
Lymphoproliferative Disorders
0.100 Biomarker group BEFREE CD30+ lymphoproliferative disorders of the skin: still an open question. 23149700 2012
CUI: C0024314
Disease: Lymphoproliferative Disorders
Lymphoproliferative Disorders
0.100 Biomarker group BEFREE Lymphomatoid papulosis (LyP) belongs to the spectrum of primary cutaneous CD30-positive lymphoproliferative disorders. 23026936 2013
CUI: C0024314
Disease: Lymphoproliferative Disorders
Lymphoproliferative Disorders
0.100 Biomarker group BEFREE Primary cutaneous anaplastic large cell lymphoma is regarded as an ALK-negative variant confined to the skin and is part of the spectrum of primary cutaneous CD30-positive T-cell lymphoproliferative disorders. 22773605 2013
CUI: C0024314
Disease: Lymphoproliferative Disorders
Lymphoproliferative Disorders
0.100 Biomarker group BEFREE Once a diagnosis of lymphoma is established, it is important to exclude systemic anaplastic lymphoma kinase-negative ALCL involving the breast, primary cutaneous ALCL, and other CD30(+) lymphoproliferative disorders. 24878027 2014