Sau P, Lupton G P, Graham J H
Department of Dermatology, Walter Reed Army Medical Center, Washington, DC 20307-5001.
J Cutan Pathol. 1992 Oct;19(5):357-65. doi: 10.1111/j.1600-0560.1992.tb00606.x.
We report 14 cases of trichogerminoma, a rare form of cutaneous adnexal neoplasm, derived from hair germ epithelium. The neoplasms occurred in 9 men and 5 women. Their ages ranged from 16 to 73 years (median 53 years). The tumors were slow growing, asymptomatic dermal or subcutaneous nodules, located on the head and neck (6), trunk (4), extremities (2) and hip (1), with no distinguishing clinical features. Histologically, trichogerminomas were characterized by sharply circumscribed, pseudoencapsulated dermal and subcutaneous nodules, ranging in size from 0.4 to 4.0 cm in diameter (mean 1.9 cm). The nodules were subdivided into lobules separated by variable amounts of stroma that demonstrated varying cellularity and mucin content. The lobules were composed of basaloid cells that formed densely packed, round nests or "cell balls" resembling hair bulbs. The basaloid cells demonstrated peripheral palisading, keratinization and differentiation towards various pilosebaceous structures. Retraction spaces, well developed hair follicles and hair shafts were not observed. These distinctive histologic features separated these neoplasms from other tumors of pilar origin and from basal cell carcinoma. The trichogerminomas behaved in a benign fashion with one exception. Complete excision of the lesions is the treatment of choice.
我们报告了14例毛发芽瘤,这是一种罕见的皮肤附属器肿瘤,起源于毛芽上皮。这些肿瘤发生在9名男性和5名女性中。他们的年龄在16至73岁之间(中位年龄53岁)。肿瘤生长缓慢,为无症状的真皮或皮下结节,位于头颈部(6例)、躯干(4例)、四肢(2例)和臀部(1例),无明显临床特征。组织学上,毛发芽瘤的特征是界限清楚、假包膜形成的真皮和皮下结节,直径从0.4至4.0厘米不等(平均1.9厘米)。结节被不同数量的间质分隔成小叶,间质显示出不同的细胞密度和粘蛋白含量。小叶由基底样细胞组成,这些细胞形成紧密堆积的圆形巢或类似毛球的“细胞球”。基底样细胞表现出周边栅栏状排列、角化以及向各种毛囊皮脂腺结构的分化。未观察到退缩间隙、发育良好的毛囊和毛干。这些独特的组织学特征将这些肿瘤与其他毛囊起源的肿瘤以及基底细胞癌区分开来。除1例例外,毛发芽瘤表现为良性。病变的完整切除是首选治疗方法。