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Reappraisal of the provisional entity primary cutaneous CD4+ small/medium pleomorphic T-cell lymphoma: a series of 10 adult and pediatric patients and review of the literature.
Baum, Christian L; Link, Brian K; Neppalli, Vishala T; Swick, Brian L; Liu, Vincent.
Affiliation
  • Baum CL; Department of Dermatology, University of Iowa Hospitals and Clinics, Iowa City, Iowa.
  • Link BK; Department of Internal Medicine, University of Iowa Hospitals and Clinics, Iowa City, Iowa.
  • Neppalli VT; Department of Pathology, University of Iowa Hospitals and Clinics, Iowa City, Iowa.
  • Swick BL; Department of Dermatology, University of Iowa Hospitals and Clinics, Iowa City, Iowa; Department of Pathology, University of Iowa Hospitals and Clinics, Iowa City, Iowa.
  • Liu V; Department of Dermatology, University of Iowa Hospitals and Clinics, Iowa City, Iowa; Department of Pathology, University of Iowa Hospitals and Clinics, Iowa City, Iowa. Electronic address: vincent-liu@uiowa.edu.
J Am Acad Dermatol ; 65(4): 739-748, 2011 Oct.
Article in En | MEDLINE | ID: mdl-21641676
BACKGROUND: Primary cutaneous CD4(+) small/medium-sized pleomorphic T-cell lymphoma (PCSM-TCL) was defined as a provisional entity in the 2005 World Health Organization-European Organization for Research and Treatment of Cancer classification of cutaneous lymphomas. A limited number of reports describe a generally indolent but heterogeneous condition. OBJECTIVE: We reviewed the concept of PCSM-TCL when applied to our experience and to the published literature. METHODS: We conducted a retrospective chart review and a PubMed search to identify all reported cases of PCSM-TCL from 2005 to 2010. RESULTS: Ten patients, including 4 of the youngest described, were identified in our institution, and their clinical and pathologic features were analyzed. All had a benign clinical course. Ten reports of patients with PCSM-TCL were reviewed and commonalities were found within an otherwise variable spectrum of clinical presentation, pathology, and biologic behavior. LIMITATIONS: This study was retrospective, follow-up was short term in some cases, and data were limited in a number of published reports. CONCLUSIONS: Our experience of 10 cases that met the diagnostic criteria of the provisional entity PCSM-TCL highlights its occurrence in children and further supports characterization of this condition as a clonal T-cell lymphoproliferative disorder with indolent behavior.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Lymphoma, T-Cell, Cutaneous Type of study: Observational_studies / Prognostic_studies Limits: Adolescent / Adult / Aged80 / Child / Female / Humans / Male / Middle aged Language: En Journal: J Am Acad Dermatol Year: 2011 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Lymphoma, T-Cell, Cutaneous Type of study: Observational_studies / Prognostic_studies Limits: Adolescent / Adult / Aged80 / Child / Female / Humans / Male / Middle aged Language: En Journal: J Am Acad Dermatol Year: 2011 Document type: Article Country of publication: United States