Mahler C, Verhelst J, Klaes R, Trouillas J
Department of Endocrinology and Neurosurgery, Middelheim Hospital, Antwerp, Belgium.
Pathol Res Pract. 1991 Jun;187(5):598-602. doi: 10.1016/S0344-0338(11)80153-6.
A 36-year-old man with depression, Cushingoid features and hypogonadism was found to have simultaneous pituitary-dependent Cushing's disease and marked elevation of serum prolactin (PRL). CT-scan revealed a macroadenoma with suprasellar extension. Transphenoidal surgery cured the patient's Cushing's disease, but failed to correct his hyperprolactinemia, which was controlled by subsequent bromocriptine therapy. Immunostaining of the pituitary tumor was positive for PRL as well as for ACTH, and ACTH-related peptides beta-lipotropin and beta-endorphin in two distinct tumor cell lines. This pituitary tumor is one of the few mixed PRL- and ACTH-secreting tumors documented by immunostaining. It is the second reported in a macroadenoma, in which PRL-secreting tumoral cells are much more abundant than ACTH-secreting cells.
一名36岁男性,有抑郁症、库欣样特征和性腺功能减退,被发现同时患有垂体依赖性库欣病和血清催乳素(PRL)显著升高。CT扫描显示有一个向鞍上延伸的大腺瘤。经蝶窦手术治愈了患者的库欣病,但未能纠正其高催乳素血症,随后通过溴隐亭治疗得以控制。垂体肿瘤的免疫染色显示PRL以及促肾上腺皮质激素(ACTH)呈阳性,并且在两种不同的肿瘤细胞系中ACTH相关肽β-促脂素和β-内啡肽也呈阳性。该垂体肿瘤是少数经免疫染色证实的同时分泌PRL和ACTH的混合性肿瘤之一。这是在大腺瘤中报道的第二例,其中分泌PRL的肿瘤细胞比分泌ACTH的细胞丰富得多。