Ottery F D, Carlson R A, Gould H, Weese J L
J Comput Assist Tomogr. 1986 Mar-Apr;10(2):260-3. doi: 10.1097/00004728-198603000-00017.
Retrorectal cyst-hamartomas (RRCH) are congenital lesions characterized by the presence of cysts lined by multiple types of epithelium, often predominantly mucin-secreting. Three cases of RRCH are presented with their associated histologic and CT findings. The lesion requires complete surgical excision to prevent complications of recurrence, infection, or metastasis.
直肠后囊肿性错构瘤(RRCH)是先天性病变,其特征为存在由多种上皮细胞衬里的囊肿,通常以分泌粘蛋白为主。本文报告3例RRCH及其相关的组织学和CT表现。该病变需要完整手术切除以预防复发、感染或转移等并发症。