Clinical Features

JG-CTCL manifests with poikilodermatous patchy or nodular, localized or disseminated skin lesions (Fig. 1), with onset in childhood or early adulthood (median age of six reported patients is 13 years, ranging from 4 to 23 years)(1). The course of the disease is slowly progressive. Several years to decades after disease onset, half of the patients develop nodal Hodgkin lymphoma or systemic large cell anaplastic CD30+ lymphoma.

Figure 1 Infiltrated, hyperpigmented areas on the back.
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