Hypopigmented mycosis fungoides (HMF) is the most common variant of mycosis fungoides (MF) in children. Large-cell transformation in HMF has never been reported. Herein we report a case of HMF in an 8-year-old boy who presented with a 6-year history of hypopigmented patches on the bilateral arms, lower back, buttocks, posterior thighs, and lower legs. Biopsy revealed an abnormal CD8(+) epidermotropic T-cell infiltrate consistent with the diagnosis of MF. The T-cell clonality study was positive. The patient was started on narrowband ultraviolet B (NBUVB) phototherapy and topical steroids. He had a 50% reduction in his patches after 10 months of treatment, after which he developed a single annular plaque on his left thigh. The biopsy specimen demonstrated large cells that were diffusely CD8(+) and CD30(-). Clobetasol propionate ointment was prescribed, which led to complete resolution of the plaque within 2 weeks. NBUVB phototherapy was continued and the patient had a complete response within the following 5 months. The case is an example of exceptionally rare large-cell transformation in pediatric MF and stresses the importance of regular follow-up of these patients.
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Department of Oncology and Diagnostic Sciences, School of Dentistry, University of Maryland, Baltimore, 21201, MDDepartment of Oncology and Diagnostic Sciences, School of Dentistry, University of Maryland, Baltimore, 21201, MD
Sultan A.S.
Mostoufi B.
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Department of Oral and Maxillofacial Surgery, School of Dentistry, University of Maryland, Baltimore, 21201, MDDepartment of Oncology and Diagnostic Sciences, School of Dentistry, University of Maryland, Baltimore, 21201, MD
Mostoufi B.
Papadimitriou J.C.
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Department of Pathology, University of Maryland School of Medicine, Baltimore, 21201, MDDepartment of Oncology and Diagnostic Sciences, School of Dentistry, University of Maryland, Baltimore, 21201, MD
Papadimitriou J.C.
Koka R.
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Department of Pathology, University of Maryland School of Medicine, Baltimore, 21201, MDDepartment of Oncology and Diagnostic Sciences, School of Dentistry, University of Maryland, Baltimore, 21201, MD
Koka R.
Basile J.
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Department of Oncology and Diagnostic Sciences, School of Dentistry, University of Maryland, Baltimore, 21201, MD
University of Maryland Greenebaum Cancer Center, Baltimore, 21201, MDDepartment of Oncology and Diagnostic Sciences, School of Dentistry, University of Maryland, Baltimore, 21201, MD
Basile J.
Younis R.H.
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Department of Oncology and Diagnostic Sciences, School of Dentistry, University of Maryland, Baltimore, 21201, MD
University of Maryland Greenebaum Cancer Center, Baltimore, 21201, MDDepartment of Oncology and Diagnostic Sciences, School of Dentistry, University of Maryland, Baltimore, 21201, MD