 |
 |

Secondary Malignant Neoplasms in 71 Patients With Sézary Syndrome
Julia J. Scarisbrick, MRCP;
Fiona J. Child, MRCP;
Alun V. Evans, MRCP;
Elisabeth A. Fraser-Andrews, MRCP;
Margaret Spittle, FRCR;
Robin Russell-Jones, FRCP
Arch Dermatol. 1999;135:1381-1385.
Background Sézary syndrome (SS) is characterized by a malignant proliferation of CD4+ve T cells, which may result in a degree of immunoparesis. Immunosuppression is associated with an increased incidence of internal malignant neoplasms and a high rate of nonmelanoma skin cancer, particularly squamous cell carcinoma. Therefore, we reviewed the incidence of secondary malignant neoplasms in patients with SS.
Observations Of 71 patients with SS, 16 (23%) developed 19 secondary and tertiary malignant neoplasms. These malignant neoplasms included 8 cutaneous squamous cell carcinomas, 2 squamous cell carcinomas of the oral mucosa, and 9 other internal malignant neoplasms. The incidence of internal malignant neoplasms was twice that reported in patients of similar age treated for Hodgkin disease (P = .02). Furthermore, the incidence of cutaneous squamous cell carcinoma in the cohort was 42 times that observed in a study conducted in England of an age-matched population (1657 per 1 x 105vs 39 per 1 x 105person-years [95% confidence interval, 626-2856]).
Conclusions A number of therapeutic modalities for SS are known to be carcinogenic. We compared the different therapeutic modalities received by our patients and found no significant difference between the total cohort of patients with SS and the patients who developed secondary malignant neoplasms. These data indicate that the high incidence of secondary malignant neoplasms in patients with SS is due, at least in part, to the disease itself. The clonal proliferation of CD4+ve T cells and the relative lymphopenia (compared with a healthy population) of nonneoplastic T cells may result in compromised immunosurveillance, so that early neoplasia, whether arising spontaneously or as a result of therapy, are not dealt with appropriately.
From the Skin Tumour Unit, St John's Institute of Dermatology, St Thomas' Hospital, London, England.
RELATED ARTICLE
Archives of Dermatology Reader's Choice: Continuing Medical Education
Arch Dermatol. 1999;135(11):1423-1424.
FULL TEXT
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES
Second Lymphomas and Other Malignant Neoplasms in Patients With Mycosis Fungoides and Sezary Syndrome: Evidence From Population-Based and Clinical Cohorts
Huang et al.
Arch Dermatol 2007;143:45-50.
ABSTRACT
| FULL TEXT
Profound loss of T-cell receptor repertoire complexity in cutaneous T-cell lymphoma
Yawalkar et al.
Blood 2003;102:4059-4066.
ABSTRACT
| FULL TEXT
Prognostic significance of tumor burden in the blood of patients with erythrodermic primary cutaneous T-cell lymphoma
Scarisbrick et al.
Blood 2001;97:624-630.
ABSTRACT
| FULL TEXT
Sezary Syndrome Increases Risk for Secondary Malignancies
Journal Watch Dermatology 2000;2000:13-13.
FULL TEXT
|