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特发性中枢性尿崩症患儿和青年中抗 rabphilin-3A 抗体的缺失:阐明肿瘤病因的潜在线索。

Absence of anti-rabphilin-3A antibodies in children and young adults with idiopathic central diabetes insipidus: a potential clue to elucidating a tumor etiology.

机构信息

Department of Endocrinology, Diabetes and Metabolism, Fujita Health University, 1-98 Dengakugakubo, Kutsukake-Cho, Toyoake, Aichi, 470-1192, Japan.

Department of Pediatrics, Sapporo Medical University School of Medicine, Sapporo, 060-8556, Japan.

出版信息

Hormones (Athens). 2023 Dec;22(4):747-758. doi: 10.1007/s42000-023-00484-0. Epub 2023 Sep 11.

Abstract

BACKGROUND

Central diabetes insipidus (CDI) is a rare condition caused by various underlying diseases, including neoplasms, autoimmune diseases, and infiltrative diseases. Differentiating between CDI etiologies is difficult. What has initially been classified as "idiopathic" central diabetes insipidus might in fact underlie various pathogenic mechanisms that are less understood to date and/or are not obvious at initial presentation. Therefore, even if idiopathic CDI is diagnosed at the time of onset, it is common for tumors such as germinoma to develop during surveillance. Crucially, a delayed diagnosis of germinoma may be associated with a worse prognosis. Recently, the presence of anti-rabphilin-3A antibodies has been found to be a highly sensitive and specific marker of lymphocytic infundibuloneurohypophysitis, an autoimmune-mediated CDI.

CASE PRESENTATION

We herein present two cases, namely, a 13-year-old boy (patient 1) and a 19-year-old young man (patient 2) who were diagnosed with idiopathic CDI. In both patients, panhypopituitarism developed. Magnetic resonance imaging revealed pituitary stalk thickening and pituitary swelling approximately 1 1/2 years after the onset of CDI. Western blotting did not reveal the presence of anti-rabphilin-3A antibodies in serum in either patient, suggesting that autoimmune mechanisms might not be involved. Both patients were subsequently diagnosed with germinoma on pathological examination. They received chemotherapy, followed by radiation therapy. Notably, testosterone and insulin-like growth factor-1 levels normalized, and libido and beard growth recovered after chemoradiotherapy in patient 2.

CONCLUSION

Our data suggest that the absence of anti-rabphilin-3A antibodies in young patients clinically diagnosed with idiopathic CDI may increase the probability of the development of non-lymphocytic lesions, including germinoma. We thus recommend a more attentive approach at the onset of these diseases.

摘要

背景

中枢性尿崩症(CDI)是一种由多种潜在疾病引起的罕见病症,包括肿瘤、自身免疫性疾病和浸润性疾病。区分 CDI 的病因较为困难。最初被归类为“特发性”中枢性尿崩症的患者,其病因可能实际上是目前了解较少的各种发病机制,或者在初始表现时并不明显。因此,即使在发病时诊断为特发性 CDI,在随访期间也常发生生殖细胞瘤等肿瘤。至关重要的是,生殖细胞瘤的延迟诊断可能与预后较差相关。最近,抗 rabphilin-3A 抗体的存在被发现是淋巴细胞性漏斗神经垂体炎(一种自身免疫介导的 CDI)的高度敏感和特异性标志物。

病例介绍

我们在此介绍两例病例,一例为 13 岁男孩(患者 1),另一例为 19 岁年轻男性(患者 2),他们均被诊断为特发性 CDI。在这两例患者中,均出现了全垂体功能减退症。磁共振成像显示,在 CDI 发病后约 1 年半,垂体柄增粗和垂体肿胀。Western blot 分析未在两例患者的血清中发现抗 rabphilin-3A 抗体,提示可能不存在自身免疫机制。随后,两例患者均通过病理检查诊断为生殖细胞瘤。他们接受了化疗,随后进行了放疗。值得注意的是,患者 2 在放化疗后,睾酮和胰岛素样生长因子-1 水平恢复正常,性欲和胡须生长恢复。

结论

我们的数据表明,临床上诊断为特发性 CDI 的年轻患者血清中缺乏抗 rabphilin-3A 抗体可能增加非淋巴细胞性病变(包括生殖细胞瘤)发生的可能性。因此,我们建议在这些疾病的发病初期更应保持警惕。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3121/10651553/10012b127ebf/42000_2023_484_Fig1_HTML.jpg

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