Wong T Y, Reed J A, Suster S, Flynn S D, Mihm M C
Dermatopathology Division, Massachusetts General Hospital, Boston.
Histopathology. 1993 Jun;22(6):575-80. doi: 10.1111/j.1365-2559.1993.tb00179.x.
We report two cases of a rare benign tumour of hair germ. Clinically, both were solitary, well-circumscribed, subcutaneous nodules located in the extremities. Histologically, the tumours were characterized by nests and thin cords of basaloid epithelial cells intimately associated with a cellular stroma. The basaloid cells exhibited peripheral palisading, keratinization in the form of keratotic cysts and squamoid transformation, and pilar differentiation. An unusual, but distinctive, cribriform pattern of growth was observed. There was no communication with the overlying epidermis. Abundant primitive hair germinal buds and rare more advanced abortive hair follicles were identified. These histological appearances encompass features of both trichoblastic fibroma and trichogenic trichoblastoma, thus distinguishing these neoplasms from other skin tumours and reinforcing the hypothesis that these tumours are closely related from a histogenetic point of view. The presence of overlapping histological features can be problematic for practising histopathologists who rarely encounter these conditions. With this in mind, the term benign trichogenic tumour may be more appropriate to encompass these two tumours and related neoplasms that appear to lie within the spectrum of hair follicle development.
我们报告了两例罕见的毛芽良性肿瘤。临床上,两例均为孤立的、边界清晰的皮下结节,位于四肢。组织学上,肿瘤的特征是基底样上皮细胞巢和细索,与细胞性间质紧密相连。基底样细胞表现为周边栅栏状排列、以角化囊肿形式出现的角化及鳞状化生,以及毛干分化。观察到一种不寻常但独特的筛状生长模式。与上方表皮无连通。发现大量原始毛生发芽和罕见的更高级的发育不全毛囊。这些组织学表现包含了毛母质纤维瘤和毛源性毛母细胞瘤的特征,从而将这些肿瘤与其他皮肤肿瘤区分开来,并强化了从组织发生学角度来看这些肿瘤密切相关的假说。对于很少遇到这些情况的执业组织病理学家来说,组织学特征重叠的情况可能会造成问题。考虑到这一点,术语“良性毛源性肿瘤”可能更适合涵盖这两种肿瘤以及似乎处于毛囊发育谱系内的相关肿瘤。