Central diabetes insipidus: A rare primary manifestation of small-cell lung carcinoma.

IF 1.1 Q4 PRIMARY HEALTH CARE
S Kavya, Avinash H Rajanna, Naval Kishore, Aditya Chandrashekar
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Abstract

Diabetes insipidus (DI) is a disorder of water hemostasis that is associated with polyuria-polydipsia syndrome. Central DI (CDI) primarily results from autoimmune destruction, traumatic injury, or anatomical damage caused by neoplasms. Craniopharyngioma, germinoma, and distant metastases are the main neoplastic causes, with pituitary adenomas rarely manifesting as CDI. Pituitary gland metastasis is rare, with the vast majority of cases being asymptomatic. We present a rare case of pituitary metastasis originating from small-cell carcinoma of the lung with CDI and skin swellings as the primary manifestation, without any evidence of the primary malignancy upon initial presentation. A 56-year-old chronic smoker with newly diagnosed type-2 diabetes mellitus presented with a history of polydipsia and polyuria along with soft tissue swellings in the axilla and the chest for the last 3 months. A water deprivation test and a desmopressin challenge test were performed, revealing the presence of CDI. In light of the CDI, a contrast-enhanced magnetic resonance imaging brain was performed, which displayed a loss of pituitary bright spot and four T2 isointense lesions with post-contrast enhancement in the left frontal, parietal, occipital, and right temporal lobes, suggestive of metastatic lesions. Fine needle aspiration cytology of the swelling revealed cytomorphological characteristics indicating the presence of malignancy, specifically favoring carcinoma. Contrast-enhanced computed tomography thorax revealed a right hilar lung mass infiltrating the surrounding structures with multiple regional and distant metastases. A lung biopsy confirmed the presence of small-cell lung carcinoma (SCLC). The final diagnosis was advanced SCLC with multiple distant metastases associated with CDI, and the patient is currently receiving palliative care and inhalational desmopressin. In conclusion, metastatic lesions and lung cancer must be considered early when patients present with polydipsia and polyuria symptoms.

中枢性糖尿病:小细胞肺癌的一种罕见原发表现。
糖尿病性尿崩症(DI)是一种与多尿多脂综合征相关的止水障碍。中枢性尿崩症(CDI)主要源于自身免疫性破坏、外伤或肿瘤造成的解剖学损伤。颅咽管瘤、生殖细胞瘤和远处转移是主要的肿瘤病因,垂体腺瘤很少表现为 CDI。垂体转移罕见,绝大多数病例无症状。我们报告了一例罕见的垂体转移瘤病例,该病源于肺小细胞癌,以CDI和皮肤肿胀为主要表现,最初发病时没有任何原发恶性肿瘤的证据。一名 56 岁的新诊断 2 型糖尿病患者长期吸烟,近 3 个月来出现多尿多饮症状,同时伴有腋窝和胸部软组织肿胀。患者接受了缺水试验和去氨加压素挑战试验,结果显示其患有 CDI。鉴于 CDI,该患者接受了对比增强脑磁共振成像检查,结果显示垂体亮点消失,左侧额叶、顶叶、枕叶和右侧颞叶出现四个 T2 等密度病灶,且对比后增强,提示为转移性病灶。肿物的细针穿刺细胞学检查显示,细胞形态学特征表明存在恶性肿瘤,尤其是癌。胸部对比增强计算机断层扫描显示,右侧肺门肿块浸润周围结构,并伴有多个区域和远处转移灶。肺部活检证实了小细胞肺癌(SCLC)的存在。最终诊断为晚期SCLC,伴有CDI的多发远处转移,患者目前正在接受姑息治疗和吸入去氨加压素。总之,当患者出现多尿和多尿症状时,必须及早考虑转移性病灶和肺癌。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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7.10%
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40 weeks
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