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

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

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 γ and δ-T-cell lymphoma (CGD-TCL). Because of its rarity and inability to study large number of patients,...

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Veröffentlicht in:Indian journal of dermatology 2017-03, Vol.62 (2), p.200-202, Article 200
Hauptverfasser: Jagati, Ashish, Shah, Bela J, Tibrewal, Sonal, Gajjar, Trusha
Format: Artikel
Sprache:eng
Schlagworte:
Care and treatment
Case Report
Case studies
Development and progression
Epidermotropism
immunohistochemistry
Non-Hodgkin's lymphomas
Physiological aspects
primary cutaneous gamma/delta–T-cell lymphoma
T cells
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Zusammenfassung: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 γ and δ-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.
ISSN:0019-5154
1998-3611
DOI:10.4103/ijd.IJD_440_16