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Low-Grade Cutaneous B-cell Lymphoma in African American Patients
Insights
Cutaneous marginal zone lymphoma (CMZL) and cutaneous follicle center lymphoma (CFCL) present earlier in African American patients, often with more widespread skin involvement but still follow an indolent course with no reported deaths.
Area of Science:
- Dermatology
- Oncology
- Hematology
Background:
- Cutaneous marginal zone lymphoma (CMZL) and cutaneous follicle center lymphoma (CFCL) are rare indolent cutaneous B-cell lymphomas (CBCL).
- African American (AA) patients have a very low incidence of CBCL, with limited data on disease presentation and progression in this demographic.
- Previous research suggests cutaneous T-cell lymphomas may be more aggressive in AA individuals, highlighting a need for data on CBCL in this population.
Purpose of the Study:
- To characterize the clinical presentation, disease course, and demographics of CMZL and CFCL in African American patients.
- To compare the features of CMZL/CFCL in AA patients with those in white patients.
- To assess the incidence of systemic disease and outcomes in AA patients with CMZL/CFCL.
Main Methods:
- Retrospective chart review of 10 African American patients diagnosed with CMZL/CFCL.
- Comparison of demographic data, clinical features, and systemic disease incidence between AA and white patient cohorts.
- Analysis of disease presentation (T-classification), site of involvement, and extracutaneous disease at initial staging.
Main Results:
- Out of 288 CMZL/CFCL patients, 10 (3.5%) were AA. AA patients were diagnosed at a younger median age (41 vs. 54 years) compared to white patients.
- AA patients presented with more extensive cutaneous disease (T2-T3 in 70%) and more frequent head and neck involvement.
- No significant difference in extracutaneous systemic disease at initial staging was observed between AA and white patients. No deaths were reported in the AA cohort.
Conclusions:
- CMZL and CFCL in African American patients exhibit an earlier age of onset and a higher T-classification at presentation, with a predilection for head and neck involvement.
- Despite these distinct features, CMZL/CFCL appears to follow an indolent course in the AA population, with uncommon systemic involvement and no reported mortality.
- Larger studies are warranted to validate these findings and further elucidate the behavior of CMZL/CFCL in African Americans.
Abstract:
Introduction: Cutaneous marginal zone lymphoma (CMZL) and cutaneous follicle center lymphoma (CFCL) are rare indolent cutaneous B-cell lymphomas (CBCL). Their incidence in African American (AA) patients is extremely low. While cutaneous T-cell lymphomas appear to be more aggressive in AA individuals, there is no data on the presentation and course of disease of CBCL in this group. In this study, we aimed to characterize CMZL/CFCL in AA patients. Methods: A retrospective chart review identified 10 AA patients with CMZL/CFCL. We compared demographics, clinical features, and systemic disease incidence between AA and white patients. Results: Of 288 patients with CMZL/CFCL, 10 patients were AA (3.5%), and 266 were white. AA patients trended toward diagnosis at a younger age compared to white individuals (median age of 41 vs 54 years; P=0.07). AAs presented with more regional and generalized cutaneous disease (T2-T3 in 70%), while most white patients presented with a solitary lesion (T1 in 55%). Head and neck involvement was more common in AA patients. Extracutaneous systemic disease at initial staging was not significantly different between the groups. One AA patient with primary CMZL developed extracutaneous MZL after16 years. No deaths were reported among AAs. Discussion: CMZL/ CFCL in this series of AA patients had an earlier age of onset with preferential head and neck involvement and a higher T classification at presentation. Despite these features, systemic involvement was uncommon, and no deaths were recorded. This data supports an indolent course of CMZL and CFCL in the AA population; larger studies are needed to confirm these findings. J Drugs Dermatol. 2018;17(12):1334-1337.
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