Yamamura T, Aozasa K, Sano S
J Am Acad Dermatol. 1984 May;10(5 Pt 1):796-803. doi: 10.1016/s0190-9622(84)70095-8.
The clinical and histopathologic findings in thirty-nine cases of cutaneous lymphoma characterized by a proliferation of convoluted cells were reviewed. Thirty patients (77%) presented with erythematous or papular lesions (group I). The remaining nine patients (23%) presented with cutaneous nodules or tumors without erythematous lesions (group III). Histologically, the polymorphous infiltration was the common feature in both groups, but the presence of epidermotropism in group I was contrasted to the absence of epidermotropism in group II disease. The patients in group I had a higher median age (54 years) than those in group II (35 years), and a more favorable 3-year survival rate (44%) than that of the latter (19%). An evolution occasionally occurred from the epidermotropic to the nonepidermotropic form, followed by a poor clinical course. When the skin lesions were nonepidermotropic , irrespective of preceding clinical course, the prognosis was poor.
对39例以卷曲细胞增殖为特征的皮肤淋巴瘤的临床和组织病理学发现进行了回顾。30例患者(77%)表现为红斑或丘疹性病变(I组)。其余9例患者(23%)表现为无红斑病变的皮肤结节或肿瘤(III组)。组织学上,两组的共同特征是多形性浸润,但I组存在亲表皮性,与II组疾病不存在亲表皮性形成对比。I组患者的中位年龄(54岁)高于II组(35岁),3年生存率(44%)也比后者(19%)更有利。偶尔会出现从亲表皮性形式向非亲表皮性形式的演变,随后临床病程不佳。当皮肤病变为非亲表皮性时,无论之前的临床病程如何,预后都很差。