Folliculotropic mycosis fungoides in a child: a rare case

Authors

  • Fatima Zahoor Department of Dermatology, PNS Shifa Hospital, Karachi, Pakistan
  • Shakila Junaid Department of Dermatology, Bahria University Medical and Dental College, PNS Rahat Hospital, Karachi, Pakistan
  • Ghazal Afzal Department of Dermatology, PNS Shifa Hospital, Karachi, Pakistan

DOI:

https://doi.org/10.47391/JPMA.8348

Keywords:

Childhood tumors, hypopigmentation, melanocytes, lymphoma, CTCL, mycosis fungoides

Abstract

Folliculotropic mycosis fungoides (FMF) is a variant of mycosis fungoides characterized by infiltration of hair follicle epithelium by neoplastic lymphoid cells. Generally, it is usually typified by indurated plaques and tumours mainly on the head and neck. However, a wide range of clinical signs have been noted. The clinical presentation of FMF may include prurigo-like lesions, acneiform lesions, cysts, nodules, areas of scarring alopecia, and hypopigmented plaques or papules with follicular prominences. The average age of diagnosis is 60 years while it is rare in childhood and adolescence. We discuss the case of a 12-year-old boy patient who had an asymptomatic, erythematous, infiltrating plaque across his left nasolabial fold for three months prior to presentation. Histological assessment of lesion showed characteristic findings of follicular mucinosis with predominance of CD4+ lymphocytes and immunohistochemical studies were positive for CD3+ stains. An increased CD4:CD8 ratio and negative CD20 was also shown.

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Published

2023-10-30

How to Cite

Fatima Zahoor, Junaid, S., & Ghazal Afzal. (2023). Folliculotropic mycosis fungoides in a child: a rare case. Journal of the Pakistan Medical Association, 73(11), 2257–2259. https://doi.org/10.47391/JPMA.8348

Issue

Section

Case Report