Indian Journal of Dermatology
CASE REPORT
Year
: 2017  |  Volume : 62  |  Issue : 2  |  Page : 200--202

CD3+, CD56+, CD4−, CD8−, CD20−, CD30− Peripheral T-Cell Non-Hodgkin's Lymphoma: A Rare Case Report


Ashish Jagati, Bela J Shah, Sonal Tibrewal, Trusha Gajjar 
 Department of Skin and VD, B.J. Medical College and Civil Hospital, Ahmedabad, Gujarat, India

Correspondence Address:
Ashish Jagati
Room No. 139, First Floor, Wing No 3, OPD Building, Civil Hospital, Asarwa, Ahmedabad, Gujarat
India

Cutaneous T-cell lymphoma (CTCL) commonly presents as mycosis fungoides or Sezary syndrome, both having CD4 positivity. A subset of CTCL which lacks CD4 surface marker is classified as cutaneous g and d–T-cell lymphoma (CGD-TCL). Because of its rarity and inability to study large number of patients, the impact of immunophenotype on the clinical outcome of primary CTCL in patients is limited. We report a case of primary CGD-TCL in a 71-year-old male because of this rarity and to emphasize its aggressive nature.


How to cite this article:
Jagati A, Shah BJ, Tibrewal S, Gajjar T. CD3+, CD56+, CD4−, CD8−, CD20−, CD30− Peripheral T-Cell Non-Hodgkin's Lymphoma: A Rare Case Report.Indian J Dermatol 2017;62:200-202


How to cite this URL:
Jagati A, Shah BJ, Tibrewal S, Gajjar T. CD3+, CD56+, CD4−, CD8−, CD20−, CD30− Peripheral T-Cell Non-Hodgkin's Lymphoma: A Rare Case Report. Indian J Dermatol [serial online] 2017 [cited 2021 Oct 20 ];62:200-202
Available from: https://www.e-ijd.org/article.asp?issn=0019-5154;year=2017;volume=62;issue=2;spage=200;epage=202;aulast=Jagati;type=0