Hill K A, Gonzalez-Crussi F, Omeroglu A, Chou P M
Department of Pathology, Children's Memorial Hospital, Northwestern University, Chicago, Illinois 60614, USA.
Pathol Res Pract. 2000;196(7):527-31. doi: 10.1016/S0344-0338(00)80055-2.
Calcifying fibrous pseudotumor is an uncommon lesion characterized by hyalinized collagen, psammomatous or dystrophic calcifications, and a predominantly lymphoplasmacytic infiltrate. Although the pathogenesis is unclear, a possible relationship with other inflammatory "pseudotumors" has been proposed. We describe the pathology of two right neck calcifying fibrous pseudotumors present in a five-week-old female infant. The masses had many of the pathologic features of calcifying fibrous pseudotumor. The presence of a florid, mixed infiltrate, and the occurrence of more than one lesion in the same patient, favor the proposal that calcifying fibrous pseudotumor may be a sclerosing end stage of inflammatory myofibroblastic tumor. However, the presence of a previously undescribed participation of Factor XIIIa-positive cells suggests that the tumor may be of dermal dendrocyte origin.
钙化性纤维性假瘤是一种罕见病变,其特征为玻璃样变的胶原、砂粒体样或营养不良性钙化,以及以淋巴细胞和浆细胞为主的浸润。虽然发病机制尚不清楚,但有人提出它与其他炎性“假瘤”可能存在关联。我们描述了一名5周龄女婴右颈部出现的两例钙化性纤维性假瘤的病理情况。这些肿块具有钙化性纤维性假瘤的许多病理特征。存在活跃的混合性浸润,且同一患者出现不止一个病变,这支持了钙化性纤维性假瘤可能是炎性肌纤维母细胞瘤硬化终末期的观点。然而,存在以前未描述过的因子ⅩⅢa阳性细胞参与,提示该肿瘤可能起源于真皮树突状细胞。