颅咽管瘤合并Rathke裂隙囊肿2例

T Nakajou, M Morimoto, M Kurisaka, K Mori
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摘要

本文报告两例罕见的颅咽管瘤合并拉氏裂隙囊肿。患者为74岁的女性和12岁的男孩。前者主诉双侧视力下降、视野障碍伴低催乳素血症,后者主诉尿崩症、生长迟缓。这些病例的MR图像显示鞍区肿瘤,由囊性和实性成分组成。经蝶窦切除肿瘤,光镜、电镜观察肿瘤组织。囊壁由纤毛柱状细胞、黏液细胞和基底细胞三种上皮细胞组成。固体成分由层状鳞状细胞组成。这两个分量相互移动。综上所述,考虑到Rathke裂隙囊肿和颅咽管瘤均起源于Rathke囊的残余,我们认为Rathke裂隙囊肿细胞在其生长过程中有时会向颅咽管瘤分化。
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[Two cases of craniopharyngioma associated with Rathke's cleft cyst].

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.

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