Gordon Michael S, Gordon Murray B
Division of Endocrinology, Diabetes and Hypertension, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Division of Endocrinology, Allegheny Neuroendocrinology Center, Allegheny General Hospital, Drexel University College of Medicine, Pittsburgh, PA, USA.
Case Rep Endocrinol. 2016;2016:5191903. doi: 10.1155/2016/5191903. Epub 2016 Aug 30.
Etiologies of a thickened stalk include inflammatory, neoplastic, and idiopathic origins, and the underlying diagnosis may remain occult. We report a patient with a thickened pituitary stalk (TPS) and papillary thyroid carcinoma (PTC) whose diagnosis remained obscure until a skin lesion appeared. The patient presented with PTC, status postthyroidectomy, and I(131) therapy. PTC molecular testing revealed BRAF mutant (V600E, GTC>GAG). She had a 5-year history of polyuria/polydipsia. Overnight dehydration study confirmed diabetes insipidus (DI). MRI revealed TPS with loss of the posterior pituitary bright spot. Evaluation showed hypogonadotropic hypogonadism and low IGF-1. Chest X-ray and ACE levels were normal. Radiographs to evaluate for extrapituitary sites of Langerhans Cell Histiocytosis (LCH) were unremarkable. Germinoma studies were negative: normal serum and CSF beta-hCG, alpha-fetoprotein, and CEA. Three years later, the patient developed vulvar labial lesions followed by inguinal region skin lesions, biopsy of which revealed LCH. Reanalysis of thyroid pathology was consistent with concurrent LCH, PTC, and Hashimoto's thyroiditis within the thyroid. This case illustrates that one must be vigilant for extrapituitary manifestations of systemic diseases to diagnose the etiology of TPS. An activating mutation of the protooncogene BRAF is a potential unifying etiology of both PTC and LCH.
垂体柄增粗的病因包括炎症性、肿瘤性和特发性起源,其潜在诊断可能仍不明确。我们报告了一名患有垂体柄增粗(TPS)和甲状腺乳头状癌(PTC)的患者,其诊断在出现皮肤病变之前一直不明。该患者表现为PTC,已行甲状腺切除术及碘-131治疗。PTC分子检测显示BRAF突变(V600E,GTC>GAG)。她有5年多尿/多饮病史。夜间脱水试验证实为尿崩症(DI)。MRI显示垂体柄增粗,垂体后叶亮点消失。评估显示低促性腺激素性性腺功能减退和胰岛素样生长因子-1水平低。胸部X线和血管紧张素转换酶水平正常。评估朗格汉斯细胞组织细胞增多症(LCH)垂体外部位的X线片无异常。生殖细胞瘤检查结果为阴性:血清和脑脊液β-人绒毛膜促性腺激素、甲胎蛋白和癌胚抗原均正常。三年后,患者出现外阴唇病变,随后腹股沟区皮肤病变,活检显示为LCH。对甲状腺病理的重新分析与甲状腺内同时存在LCH、PTC和桥本甲状腺炎一致。该病例表明,必须警惕系统性疾病的垂体外表现,以诊断TPS的病因。原癌基因BRAF的激活突变可能是PTC和LCH的潜在共同病因。