Samaratunga H, Searle J, O'Loughlin B
Department of Anatomical Pathology, Royal Brisbane Hospital, Queensland.
Pathology. 1996 Jan;28(1):8-11. doi: 10.1080/00313029600169413.
A 49 year old man presented with a mass in the inguinal region that for 3 mths had been associated with slight discomfort. Clinically the mass was thought to be an enlarged lymph node. Histology however showed nodular fasciitis. There was also an associated smaller lesion that was histologically identical and which involved the wall of a medium sized vein with protrusion into its lumen. These appearances were typical of intravascular fasciitis. Review of the Royal Brisbane Hospital Pathology files for 12 yrs from 1982, revealed no other such cases. We describe here the clinical and pathological features of this case and review the literature on this rare condition.
一名49岁男性因腹股沟区肿物就诊，该肿物已存在3个月，伴有轻微不适。临床考虑该肿物为肿大淋巴结。然而，组织学检查显示为结节性筋膜炎。还存在一个较小的相关病变，组织学表现与之相同，累及一条中等大小静脉的管壁，并突入管腔。这些表现是血管内筋膜炎的典型特征。回顾皇家布里斯班医院1982年以来12年的病理档案，未发现其他类似病例。我们在此描述该病例的临床和病理特征，并复习有关这种罕见疾病的文献。
