Section of Dermatopathology, Department of Dermatology, Boston University Chobanian Avedisian School of Medicine, Boston, Massachusetts, USA.
J Cutan Pathol. 2024 Apr;51(4):267-271. doi: 10.1111/cup.14584. Epub 2023 Dec 23.
Sclerotic fibroma (SF) is a rare subset of dermal fibromas that occurs sporadically or in association with Cowden syndrome (CS). We report a case of a patient with known CS and a solitary lesion on the scalp. Histologic examination demonstrated a well-circumscribed lesion with sclerotic dermis and a whorled collagen pattern, multinucleated giant cells, and dendritic spindle cells. Nuclear atypia or mitotic figures were not noted. The giant cells were negative for Melan-A, SOX-10, EMA, SOX-10, and factor XIIIa. These findings are consistent with a giant cell collagenoma (GCC). Despite possible overlap with SF, GCC has not been associated with CS. This makes our case unique and suggests that GCC should be included in the spectrum of CS-associated cutaneous lesions. The diagnosis of SF may lead to the identification of previously undiagnosed CS; accordingly, GCC, even when present as a solitary lesion, may indicate the need for further work-up and screening for CS.
硬化性纤维瘤(SF)是一种罕见的皮肤纤维瘤亚群,偶发或与考登综合征(CS)相关。我们报告了一例已知 CS 患者和头皮单发病变。组织学检查显示边界清楚的病变,有硬化的真皮和漩涡状胶原模式、多核巨细胞和树突状梭形细胞。未见核异型性或有丝分裂象。巨细胞对 Melan-A、SOX-10、EMA、SOX-10 和因子 XIIIa 均为阴性。这些发现与巨细胞胶原瘤(GCC)一致。尽管与 SF 可能有重叠,但 GCC 与 CS 无关。这使得我们的病例独特,并表明 GCC 应包括在 CS 相关皮肤病变的范围内。SF 的诊断可能导致以前未诊断出的 CS 的识别;因此,即使 GCC 作为单发病变存在,也可能表明需要进一步检查和筛查 CS。