Kikuchi A, Shimizu H, Nishikawa T
Department of Dermatology, Keio University School of Medicine, Tokyo, Japan.
Dermatology. 1996;192(4):360-3. doi: 10.1159/000246414.
Pigmentary changes in mycosis fungoides are not rare. Although poikiloderma and hypopigmented skin lesions have often been reported in the literature, there are few cases of mycosis fungoides presenting as a hyperpigmented skin lesion. We present a 57-year-old Japanese male with mycosis fungoides whose skin lesions showed marked hyperpigmentation. The skin lesion initially appeared as an irregularly shaped itchy annular erythema with central pigmentation predominantly on his extremities. During our 5-year follow-up, these skin lesions gradually increased in size and number. The erythema extended peripherally and became elevated with marked hyperpigmentation. Histology revealed extreme elongation of the rete ridges with infiltration of atypical large lymphoid cells characteristic of mycosis fungoides and numerous melanin granules in both the epidermal melanocytes and dermal melanophages. Although the exact mechanism of the marked hyperpigmentation is one of the unique characteristics in mycosis fungoides, especially in non-white individuals.
蕈样肉芽肿中的色素改变并不罕见。虽然文献中经常报道斑驳病样皮肤异色症和色素减退性皮肤病变,但很少有蕈样肉芽肿表现为色素沉着过度性皮肤病变的病例。我们报告一例57岁的日本男性蕈样肉芽肿患者,其皮肤病变表现为明显的色素沉着过度。皮肤病变最初表现为形状不规则、瘙痒的环状红斑,中央色素沉着,主要位于四肢。在我们5年的随访期间,这些皮肤病变的大小和数量逐渐增加。红斑向周围扩展并隆起,伴有明显的色素沉着过度。组织学检查显示表皮嵴极度延长,有蕈样肉芽肿特征性的非典型大淋巴细胞浸润,表皮黑素细胞和真皮黑素吞噬细胞内有大量黑素颗粒。尽管色素沉着过度的确切机制是蕈样肉芽肿的独特特征之一,尤其是在非白种人中。