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S. M. Breathnach, P. H. Mckee and N. P. Smith, “Hypopigmented Mycosis Fungoides: Report of Five Cases with Ultrastructural Observations,” British Journal of Dermatology, Vol. 106, No. 6, 1982, pp. 643-649. doi:10.1111/j.1365-2133.1982.tb11678.x

has been cited by the following article:

• TITLE: Hypopigmented Mycosis Fungoides in a 7-Year-Old Boy

  AUTHORS: Felipe Nazareth, Maria Victoria Quaresma, Fred Bernardes, Carlos Gustavo Carneiro Castro, Edilbert Pellegrini Nahn, Jose Augusto da Costa Nery, Mayra Carrijo Rochael, Omar Lupi

  KEYWORDS: Hypopigmented; Child; Mycosis Fungoides

  JOURNAL NAME: Journal of Cosmetics, Dermatological Sciences and Applications, Vol.2 No.2, June 21, 2012

  ABSTRACT: Hypopigmented mycosis fungoides (HMF) is an uncommon variant of cutaneous T-cell lymphoma. It is more frequent in dark-skinned people, particularly children. The HMF diagnose is difficult, especially in early stages because this condition resembles benign skin diseases. Thus is histopathological analysis very important for the diagnosis. We report a case of a 7-year-old child with widespread HMF confirmed by histopathology that showed cells tagging along the dermal/epidermal junction and extending into the epidermis in a pattern of epidermotropism and focal cell aggregates in the epidermis (Pautrier’s microabscess). We demonstrate the importance of clinical suspicion for this cutaneous neoplasia in patients with hypopigmentated lesions.