Genetic polymorphisms in immunity related genes and the Vitamin D receptor gene and risk of Cutaneous T‐cell Lymphoma in Greek population

Author(s):  
A. Velissari ◽  
E. Lakiotaki ◽  
V. Nikolaou ◽  
K.V. Argyropoulos ◽  
A. Stratigos ◽  
...  
2007 ◽  
Vol 48 (3) ◽  
pp. 156-160 ◽  
Author(s):  
Christopher CI Foo ◽  
Mark BY Tang ◽  
Tina KL Chong ◽  
Yong-Jiang Sun ◽  
Suat-Hoon Tan

Blood ◽  
2007 ◽  
Vol 110 (11) ◽  
pp. 3574-3574
Author(s):  
Kelley A. Vidulich ◽  
Rakhshandra Talpur ◽  
Roland L. Bassett ◽  
Madeleine Duvic

Abstract Most common cutaneous T-cell lymphomas (CTCL) are Mycosis fungoides (MF) and a leukemic, erythrodermic (E) variant known as Sézary Syndrome (SS). Blood (B) criteria were not previously considered for staging purposes and are evolving. E-CTCL can be divided into E-MF versus SS based on new criteria, B0-B2, published by the ISCL guidelines. Historically, overall survival (OS) of “SS” patients is 2–4 years. To determine if hematologic staging and prognostic variables affects overall survival, we retrospectively studied 1197 MF/CTCL patients seen at MDACC since 1987 from which were identified 124 (10%) patients with E-CTCL. Median age at diagnosis was 63 (range 0–89), 71 males and 53 females. Hematologic (H) stage was based on quantitative Sézary cell counts (manual or by flow as absolute CD4+26−). Overall survival curves were estimated by Kaplan and Meier and compared using log-rank tests. Median OS all 124 E-CTCL patients was 5.1 years [range=0.4–18.6]. We also considered patients divided by the H0–H4 staging system (Russell-Jones 2000). For H0–H2, OS was 7.6 years, H3 was 5.4 years, and H4 was 2.4 years (p=0.011). Treatment with systemic steroids, advanced age, increased serum LDH at presentation, WBC > 20,000 were significant prognostic factors. Large cell transformation (p=0.758), positive T-cell receptor gene rearrangement in the skin (p=0.54), stage of disease (p=0.955), prior exposure to multiple treatments (p=0.953), and CD4:CD8 ratio (p=0.068) were not significant. In conclusion, we provide evidence that absolute Sézary cell counts can be used to define three groups of patients with E-CTCL with different overall survival patterns and propose a modification to the ISCL B ratings as follows: B0, absolute Sézary cell count < 1.0 KuL−1; B1: absolute Sézary cell count ≥ 1.0–10.0 KuL−1; and B2: absolute Sézary cell count >10.0 KuL−1. Serum LDH and CD4/8 ratio may be used to estimate tumor burden, as they correlate with Sézary counts.


2013 ◽  
Vol 17 (6) ◽  
pp. 433-436 ◽  
Author(s):  
Jennifer L. MacIsaac ◽  
Chloé E. Ward ◽  
Melanie Pratt

Background: Cutaneous T-cell pseudolymphoma (CTPL) is a benign reactive T-cell lymphoproliferative subtype of pseudolymphoma. Some variants of CTPL can resemble the plaques of mycosis fungoides (MF). The vast majority of drug-induced cases have been associated with anticonvulsants. There is only one report in the literature documenting a case of vancomycin-induced CTPL. Methods: We report a cutaneous T-cell lymphoma–like eruption in a human immunodeficiency virus (HIV)-positive patient recently started on vancomycin and rifampin. Results: A skin biopsy showed several histologic features of MF with immunohistochemical and T-cell receptor gene rearrangement studies suggestive of CTPL. This atypical T-cell reaction mimicking MF completely resolved on cessation of rifampin followed by vancomycin. Conclusion: Considering drug-induced causes of MF-like histologic changes is crucial to prevent unnecessary treatment for MF.


2018 ◽  
Vol 154 (12) ◽  
pp. 1424 ◽  
Author(s):  
Irene Cabello ◽  
Pedro Alia ◽  
Xavier Pintó ◽  
Cristina Muniesa ◽  
Ricardo Fernandez-de-Misa ◽  
...  

1998 ◽  
Vol 5 (1) ◽  
pp. 11-18 ◽  
Author(s):  
L. Frank Glass ◽  
Karen L. Keller ◽  
Jane L. Messina ◽  
John Dalton ◽  
Cynthia Yag-Howard ◽  
...  

Background: Cutaneous T-cell lymphoma (CTCL) represents a spectrum of diseases composed of malignant helper T lymphocytes. An accurate diagnosis of early CTCL is difficult because of the varied clinical and histologic expressions of the disease. Methods: The authors review the epidemiology, possible risk factors, clinical manifestations, diagnostic techniques, staging, prognosis, and treatment options for CTCL. Results: The varied and often nonspecific clinical and histologic presentations of CTCL may delay diagnosis and staging, thus necessitating further studies such as immunophenotyping flow cytometry, and T-cell receptor gene rearrangement analysis. Conclusions: A multidisciplinary approach to the diagnosis, staging, and treatment of CTCL assists in optimizing outcomes from management of patients with this disease.


2008 ◽  
Vol 233 (12) ◽  
pp. 1608-1614 ◽  
Author(s):  
Ilke Hacer Onen ◽  
Abdullah Ekmekci ◽  
Muzaffer Eroglu ◽  
Ece Konac ◽  
Suleyman Yesil ◽  
...  

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