Nakajou T, Morimoto M, Kurisaka M, Mori K
Department of Neurosurgery, Kochi Medical School.
Noshuyo Byori. 1994;11(1):85-92.
Two rare cases of craniopharyngioma associated with Rathke's cleft cyst are reported. The patients were 74-year-old female and 12-year-old boy. The former complained bilateral impaired visual acuity and visual field disturbance with hypoprolactinemia, the latter complained diabetes insipidus and growth retardation. MR images of these cases demonstrated sellar resion tumors, which were composed with both cystic and solid component. Transsphenoidal tumor removal were performed to both cases, and their tumor tissues were studied by light and electron microscopy. The cyst wall were composed of three kinds of epithelial cells such as ciliated columnar cells, mucous cells and basal cells. The solid components were composed of stratified squamous cells. These two components shifted each other. For these facts, to consider that both Rathke's cleft cyst and craniopharyngioma originate in remnants of Rathke's pouch, it is concluded that Rathke's cleft cyst cells sometimes cause differentiation to craniopharyngioma on its growth process.
报告了两例与拉克氏裂囊肿相关的颅咽管瘤罕见病例。患者分别为一名74岁女性和一名12岁男孩。前者主诉双侧视力减退和视野障碍伴低催乳素血症,后者主诉尿崩症和生长发育迟缓。这些病例的磁共振成像显示鞍区肿瘤,由囊性和实性成分组成。对两例患者均进行了经蝶窦肿瘤切除术,并对其肿瘤组织进行了光镜和电镜研究。囊肿壁由三种上皮细胞组成,如纤毛柱状细胞、黏液细胞和基底细胞。实性成分由复层鳞状细胞组成。这两种成分相互转换。基于这些事实,考虑到拉克氏裂囊肿和颅咽管瘤均起源于拉克氏囊的残余部分,得出结论:拉克氏裂囊肿细胞在其生长过程中有时会分化为颅咽管瘤。