Kissiedu Juliana O, Prayson Richard A
Department of Anatomic Pathology, L25, Cleveland Clinic, 9500 Euclid Avenue, Cleveland, OH 44195, USA.
Department of Anatomic Pathology, L25, Cleveland Clinic, 9500 Euclid Avenue, Cleveland, OH 44195, USA.
J Clin Neurosci. 2016 Feb;24:141-2. doi: 10.1016/j.jocn.2015.07.006. Epub 2015 Aug 24.
We report a case of a 60-year-old man who presented with weight gain, headaches, dizziness, erectile dysfunction and decreased libido. He was found to have elevated adrenocorticotropic hormone (ACTH) and prolactin serum levels. The imaging studies revealed a 1.4 cm sella/suprasellar mass which was compressing the optic chiasm. Histologic slides of the lesion showed a pituitary adenoma, marked by a proliferation of biphenotypic appearing cells, associated with a gangliocytoma, and marked by a proliferation of atypical appearing neuronal cells arranged against a glial-appearing background. Pituitary adenoma-gangliocytomas are benign combination tumors that rarely occur in the sellar region. Adenomas in this setting are sometimes functional, and rare patients with mixed adenomas (adenomas secreting more than one hormone) have been reported. To our knowledge, there has been only one other report of a combined ACTH and prolactin-producing adenoma with gangliocytoma, reported in a patient who also had acromegaly. In our patient, the immunohistochemical stains demonstrated that the bulk of the adenoma cells stained with prolactin antibody, and scattered clusters of cells within the adenoma stained positively for ACTH. The adenoma did not stain with antibodies to any of the other anterior pituitary hormones. Postoperatively, the elevated prolactin and ACTH levels returned to normal levels and there was no evidence of residual tumor. Adequate sampling and immunohistochemistry are important in rendering a correct diagnosis and in identifying the hormone status of mixed adenoma-gangliocytomas.
我们报告一例60岁男性患者,其表现为体重增加、头痛、头晕、勃起功能障碍和性欲减退。发现他的促肾上腺皮质激素(ACTH)和催乳素血清水平升高。影像学检查显示鞍区/鞍上有一个1.4 cm的肿块,压迫视交叉。病变的组织学切片显示为垂体腺瘤,其特征为双相性细胞增殖,伴有神经节细胞瘤,且有非典型神经元细胞在胶质样背景下增殖。垂体腺瘤 - 神经节细胞瘤是罕见发生于鞍区的良性混合性肿瘤。这种情况下的腺瘤有时具有功能性,已有报道罕见的混合性腺瘤(分泌不止一种激素的腺瘤)患者。据我们所知,仅有另一例关于合并ACTH和催乳素分泌性腺瘤伴神经节细胞瘤的报道,该患者同时患有肢端肥大症。在我们的患者中,免疫组化染色显示大部分腺瘤细胞被催乳素抗体染色,腺瘤内散在的细胞簇对ACTH呈阳性染色。腺瘤对其他任何垂体前叶激素抗体均无染色。术后,升高的催乳素和ACTH水平恢复正常,且无残留肿瘤迹象。充分的取材和免疫组化对于做出正确诊断以及确定混合性腺瘤 - 神经节细胞瘤的激素状态很重要。