Altmeyer P
Arch Dermatol Res. 1979 Mar 31;264(2):161-8. doi: 10.1007/BF00431127.
We report on a case of a 40 years old female patient with a lentil-sized tumor of the left pinna present since early childhood. Histologic examination revealed pigmented granular "rankenneuroma". The lesion is unencapsulated but fairly well marginated in the dermis. It is composed of varying numbers of spindle-shaped or polyhedral cells arranged in intertwining and parallel bands separated by strands of collagen. The fascicles follow the preexisting nerve truncs. All layers of the dermis may be involved, but only rarely is the superficial subcutaneous tissue invaded. The fascicles of the tumor are generally constructed in a similar fashion. In the center one see argyrophile granular alterated unpigmented cells- Those elements are surrounded by mostly bipolar cells containing varying amounts of melanin. Silverstaining shows transition from spindle-shaped cells to granular degenerated elements. It is thought that the tumor most likely originates from the proliferation of the granular degenerated Schwann cells. The characteristic feature of tumor parenchyme is the association of the granular Schwann cells with cutaneous melanoblasts.
我们报告一例40岁女性患者,自幼年起左耳廓就有一个扁豆大小的肿瘤。组织学检查显示为色素性颗粒状“兰肯神经瘤”。该病变无包膜,但在真皮内边界相当清晰。它由数量不等的梭形或多面体细胞组成,排列成交织和平行的束状,束间由胶原纤维束分隔。束状结构沿原有神经干走行。真皮各层均可受累,但很少侵犯浅表皮下组织。肿瘤的束状结构通常以类似方式构成。在肿瘤中心可见嗜银性颗粒状变性的无色素细胞,这些细胞被大多含有不同量黑色素的双极细胞所围绕。银染色显示从梭形细胞到颗粒状变性成分的过渡。据认为,该肿瘤很可能起源于颗粒状变性的施万细胞的增殖。肿瘤实质的特征性表现是颗粒状施万细胞与皮肤成黑素细胞的联合。