Soldano Anthony C, Vazquez-Martul Eduardo, Romero J A, Prieto Victor G
Department of Surgical Pathology, The University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA.
J Cutan Pathol. 2006 Nov;33(11):749-53. doi: 10.1111/j.1600-0560.2006.00540.x.
Ossifying fibromyxoid tumor (OFMT) is an uncommon neoplasm occurring predominantly in the deep soft tissues of the trunk and proximal extremities. The lineage of this rare tumor to date is still uncertain. We present a case of a subcutaneous OFMT that recurred 8 years after initial resection. The histological findings of the primary and recurrent lesions are compared along with the histologic features possibly associated with aggressiveness. Dermatopathologists should consider OFMT in the differential diagnosis of subcutaneous neoplasms with a myxoid matrix.
骨化性纤维黏液样肿瘤(OFMT)是一种罕见肿瘤,主要发生于躯干和近端肢体的深部软组织。迄今为止,这种罕见肿瘤的起源仍不确定。我们报告一例皮下OFMT病例,该病例在初次切除8年后复发。对原发灶和复发灶的组织学发现进行了比较,并探讨了可能与侵袭性相关的组织学特征。皮肤病理学家在鉴别诊断具有黏液样基质的皮下肿瘤时应考虑到OFMT。