Kameh D S, Perez-Berenguer J L, Pearl G S
Department of Pathology, Orlando Regional Healthcare System, Fla 32806, USA.
South Med J. 2000 Aug;93(8):800-2.
Three unusual cases of a rare, tumor-like condition, lipofibromatous hamartoma, are reported. This lesion is composed of fibrous and fatty tissue that infiltrates peripheral nerves, typically on the volar aspect of the upper extremities of children and young adults. All three patients had a painless soft tissue mass of the wrist and/or hand, which followed nerve distribution, and only one patient had neurologic symptoms due to compression. Diagnosis was made by open biopsy and histologic examination.
报告了三例罕见的肿瘤样疾病——脂肪纤维瘤性错构瘤的不寻常病例。该病变由浸润周围神经的纤维组织和脂肪组织组成,通常发生于儿童和年轻人上肢的掌侧。所有三名患者手腕和/或手部均有无痛性软组织肿块,呈神经分布,仅有一名患者因压迫出现神经症状。通过开放活检和组织学检查做出诊断。