Ghezzi Andrea, Rossi Jessica, Cavallieri Francesco, Napoli Manuela, Pascarella Rosario, Rizzi Romana, Russo Marco, Salomone Gaetano, Romano Antonio, Iaccarino Corrado, Froio Elisabetta, Serra Silvia, Cozzi Salvatore, Giaccherini Lucia, Valzania Franco, Pisanello Anna
Department of Biomedical, Metabolic, and Neural Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Clinical and Experimental Medicine PhD Program, University of Modena and Reggio Emilia, Modena, Italy.
Front Oncol. 2023 Jan 4;12:1059361. doi: 10.3389/fonc.2022.1059361. eCollection 2022.
Pituitary metastases are very rare in cancer patients and often originate from lung or breast tumors. They usually occur in patients with known metastatic disease, but rarely may be the first presentation of the primary tumor.
We present the case of a 58 years-old-man who reported a three-month history of polyuria-polydipsia syndrome, generalized asthenia, panhypopituitarism and bitemporal hemianopsia. Brain-MRI showed a voluminous pituitary mass causing posterior sellar enlargement and compression of the surrounding structures including pituitary stalk, optic chiasm, and optic nerves.
The patient underwent neurosurgical removal of the mass. Histological examination revealed a poorly differentiated adenocarcinoma of uncertain origin. A total body CT scan showed a mass in the left kidney that was subsequently removed. Histological features were consistent with a clear cell carcinoma. However, endoscopic examination of the digestive tract revealed an ulcerating and infiltrating adenocarcinoma of the gastric cardia. Total body PET/CT scan with 18F-FDG confirmed an isolated area of accumulation in the gastric cardia, with no hyperaccumulation at other sites.
To the best of our knowledge, there are no reports of pituitary metastases from gastric cardia adenocarcinoma. Our patient presented with symptoms of sellar involvement and without evidence of other body metastases. Therefore, sudden onset of diabetes insipidus and visual deterioration should lead to the suspicion of a rapidly growing pituitary mass, which may be the presenting manifestation of a primary extracranial adenocarcinoma. Histological investigation of the pituitary mass can guide the diagnostic workup, which must however be complete.
垂体转移瘤在癌症患者中极为罕见,通常起源于肺部或乳腺肿瘤。它们常发生于已知有转移性疾病的患者,但很少可能是原发性肿瘤的首发表现。
我们报告了一例58岁男性患者,其有三个月多尿 - 多饮综合征、全身乏力、全垂体功能减退和双颞侧偏盲的病史。脑部磁共振成像(MRI)显示一个巨大的垂体肿块,导致蝶鞍后部扩大并压迫周围结构,包括垂体柄、视交叉和视神经。
患者接受了神经外科手术切除肿块。组织学检查显示为起源不明的低分化腺癌。全身CT扫描显示左肾有一个肿块,随后被切除。组织学特征与透明细胞癌一致。然而,消化道内镜检查显示胃贲门有溃疡性浸润性腺癌。18F - FDG全身PET/CT扫描证实胃贲门有一个孤立的积聚区域,其他部位无高代谢积聚。
据我们所知,尚无胃贲门腺癌垂体转移的报道。我们的患者表现出蝶鞍受累症状且无其他身体转移的证据。因此,突然出现尿崩症和视力恶化应引起对快速生长的垂体肿块的怀疑,这可能是原发性颅外腺癌的表现形式。垂体肿块的组织学检查可指导诊断检查,但检查必须全面。