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非肝硬化性原发性肝细胞癌继发抗利尿激素分泌异常综合征

Syndrome of inappropriate anti-diuretic hormone secondary to non-cirrhotic primary hepatocellular carcinoma.

作者信息

Eltawansy Sherif, Gomez Johnson, Liss Kenneth, Nivera Noel, Babyatsky Mark

机构信息

Department of Internal Medicine, Monmouth Medical Center, Long Branch, NJ, USA.

出版信息

Am J Case Rep. 2015 Jan 23;16:31-6. doi: 10.12659/AJCR.892370.

Abstract

BACKGROUND

The syndrome of inappropriate antidiuretic hormone secretion (SIADH) is usually seen in pulmonary malignancies, central nervous system disorders, and secondary to medications. SIADH has very rarely been encountered in primary hepatocellular carcinoma. Two cases were reported in Japan and 1 case in Spain after extensive investigation of the medical records.

CASE REPORT

We report a case of a 71-year-old man who presented with confusion, cachexia, and abdominal symptoms in the form of vomiting and abdominal discomfort. On the initial work-up, SIADH diagnosis was made. After an extensive work-up, the reason for SIADH turned out to be a newly diagnosed hepatocellular carcinoma. The precipitating factor for the cancer was not identified by history or by work-up. No metastasis was identified. Liver functions were preserved but patient was severely malnourished.

CONCLUSIONS

SIADH can occur as a para-malignant feature of the malignancy. In our case, it was related to the hepatocellular carcinoma, which is a malignancy very rare to cause SIADH.

摘要

背景

抗利尿激素分泌不当综合征(SIADH)通常见于肺部恶性肿瘤、中枢神经系统疾病以及药物所致。原发性肝细胞癌中很少见到SIADH。在对病历进行广泛调查后,日本报告了2例,西班牙报告了1例。

病例报告

我们报告1例71岁男性患者,表现为意识模糊、恶病质以及以呕吐和腹部不适形式出现的腹部症状。在初步检查中,诊断为SIADH。经过广泛检查,SIADH的病因是新诊断出的肝细胞癌。通过病史或检查未发现癌症的诱发因素。未发现转移。肝功能得以保留,但患者严重营养不良。

结论

SIADH可作为恶性肿瘤的副肿瘤特征出现。在我们的病例中,它与肝细胞癌有关,而肝细胞癌是一种非常罕见的可导致SIADH的恶性肿瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e773/4315651/ce3c75501111/amjcaserep-16-31-g001.jpg

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