Granulomatous slack skin is an uncommon cutaneous T-helper cell lympho
ma closely related to mycosis fungoides. To the best of our knowledge
this disease has not been previously described in children. We report
on an 11-year-old boy who presented with painless slack skin masses in
the neck, right axilla and arm, anterior wall of the abdomen, both in
guinal regions, and the malleolar and dorsal aspects of the feet. The
disease started 3 years earlier with erythematous lesions on the neck
and wrists. Histologic examination of a specimen from the abdominal ma
ss revealed an extensive lymphoid infiltrate with scattered multinucle
ated giant cells extending from the papillary dermis to the subcutis.
The lymphoid cells showed the following immunophenotype: CD43+ (MT1),
CD45+, CD45RO+, CD20-. The phenotype of the giant cells was lysozyme p
ositive, CD68+ and Mac387-. The tumoral lymphoid cells had clonal rear
rangement for the gene of the beta chain of the T-cell receptor (Cbeta
TCR). The disease could be controlled with systemic glucocorticoids, D
ue to the presence of many histiocytes arranged In aggregates in the p
apillary and mid-dermis, this case was initially considered to be a cu
taneous form of histiocytosis. We recommend deep and extensive biopsie
s in patients with slack skin disease.