Sakai H, Matsuo S, Matsumoto M, Iizuka H
Department of Dermatology, Asahikawa Medical College, Japan.
J Dermatol. 1996 Oct;23(10):697-702. doi: 10.1111/j.1346-8138.1996.tb02683.x.
Sézary syndrome is a leukemic variant in the spectrum of cutaneous T cell lymphomas. In some cases of cutaneous T cell lymphoma, the skin tumors or lymph nodes show morphologic changes indistinguishable from those of a large-cell lymphoma; this has been termed transformation. We report a case of Sézary syndrome who developed multiple skin tumors that showed transformation, loss of multiple pan T-cell markers (CD3, 4, 5, 7, 8), and a concomitant expression of CD30 during the course of the disease. Some of the tumors spontaneously regressed following incisional biopsy or traumatic wounds. The patient died of pneumonia five years following the transformation.
蕈样肉芽肿综合征是皮肤T细胞淋巴瘤谱系中的一种白血病变体。在某些皮肤T细胞淋巴瘤病例中,皮肤肿瘤或淋巴结表现出与大细胞淋巴瘤无法区分的形态学变化;这被称为转化。我们报告了一例蕈样肉芽肿综合征患者,该患者在疾病过程中出现了多个显示转化的皮肤肿瘤,多种泛T细胞标志物(CD3、4、5、7、8)缺失,并伴有CD30的表达。部分肿瘤在切开活检或创伤性伤口后自发消退。患者在转化后五年死于肺炎。