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Paediatric primary cutaneous marginal zone B-cell lymphoma: does it differ from its adult counterpart?
Amitay-Laish, I; Tavallaee, M; Kim, J; Hoppe, R T; Million, L; Feinmesser, M; Fenig, E; Wolfe, M E L; Hodak, E; Kim, Y H.
Afiliação
  • Amitay-Laish I; Department of Dermatology, Davidoff Center, Rabin Medical Center - Beilinson Hospital, Petach Tikva, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Tavallaee M; Department of Dermatology, Stanford Cancer Center, Stanford, CA, U.S.A.
  • Kim J; Department of Pathology, Stanford Cancer Center, Stanford, CA, U.S.A.
  • Hoppe RT; Department of Radiation Oncology, Stanford Cancer Center, Stanford, CA, U.S.A.
  • Million L; Department of Radiation Oncology, Stanford Cancer Center, Stanford, CA, U.S.A.
  • Feinmesser M; Department of Pathology, Davidoff Center, Rabin Medical Center - Beilinson Hospital, Petach Tikva, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Fenig E; Department of Radiotherapy Unit, Davidoff Center, Rabin Medical Center - Beilinson Hospital, Petach Tikva, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Wolfe MEL; Department of Dermatology, Stanford Cancer Center, Stanford, CA, U.S.A.
  • Hodak E; Department of Dermatology, Davidoff Center, Rabin Medical Center - Beilinson Hospital, Petach Tikva, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Kim YH; Department of Dermatology, Stanford Cancer Center, Stanford, CA, U.S.A.
Br J Dermatol ; 176(4): 1010-1020, 2017 Apr.
Article em En | MEDLINE | ID: mdl-27501236
ABSTRACT

BACKGROUND:

Primary cutaneous marginal zone B-cell lymphoma (PCMZL) has rarely been reported in patients younger than 20 years.

OBJECTIVES:

To report our experience with PCMZL in the paediatric/adolescent age group.

METHODS:

Medical records of patients diagnosed with PCMZL before age 20 years and managed at two cutaneous lymphoma clinics in the U.S.A. and Israel from 1992 to 2015 were reviewed.

RESULTS:

The study group included 11 patients (six girls; median age 16 years, range 6-19·5); 10 had generalized/multifocal (T3) and one had regional/localized (T2) disease. Lesions were located on the limbs in all patients and the trunk in six; two had facial lesions. Staging in all but one was based on whole-body computed tomography or positron emission tomography. Initial management in most patients included nonradiation modalities one patient with localized disease received intralesional steroids; six patients with multifocal disease received the following topical/intralesional steroids (n = 3); excision (n = 2); 'watch and wait' (n = 1). No extracutaneous progression was noted during a median follow-up of 5·5 years (mean 7·5, range 0·5-14). At present, five patients are in complete remission.

CONCLUSIONS:

Based on our data (largest series in the literature with the longest follow-up), the clinicopathological presentation and course of PCMZL in the paediatric/adolescent age group are similar to those in adults. Given the indolent course and the long life expectancy of these young patients, the cumulative risk of imaging studies and the age-related potential toxicity of treatment, especially radiation, should be taken into consideration.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article