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本文引用的文献

1
Clinical utility of systemic venous sampling of FGF23 for identifying tumours responsible for tumour-induced osteomalacia.成纤维细胞生长因子23的体静脉采样在识别肿瘤性骨软化症相关肿瘤中的临床应用
J Intern Med. 2010 Oct;268(4):390-4. doi: 10.1111/j.1365-2796.2010.02262.x.
2
Oncogenic osteomalacia: two case reports with surprisingly different outcomes.致癌性骨软化症:两例结局差异惊人的病例报告。
Arch Orthop Trauma Surg. 2009 Apr;129(4):533-9. doi: 10.1007/s00402-008-0808-2. Epub 2009 Jan 6.
3
Oncogenic hypophosphataemic osteomalacia: biomarker roles of fibroblast growth factor 23, 1,25-dihydroxyvitamin D3 and lymphatic vessel endothelial hyaluronan receptor 1.致癌性低磷性骨软化症:成纤维细胞生长因子23、1,25-二羟基维生素D3和淋巴管内皮透明质酸受体1的生物标志物作用
Eur J Endocrinol. 2008 Feb;158(2):265-71. doi: 10.1530/EJE-07-0485.
4
Acquired hypophosphatemic osteomalacia associated with multiple myeloma.与多发性骨髓瘤相关的获得性低磷性骨软化症。
Joint Bone Spine. 2005 Oct;72(5):424-6. doi: 10.1016/j.jbspin.2004.10.012. Epub 2005 Jan 26.
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Venous sampling for fibroblast growth factor-23 confirms preoperative diagnosis of tumor-induced osteomalacia.用于检测成纤维细胞生长因子-23的静脉采血证实了术前肿瘤诱导性骨软化症的诊断。
J Clin Endocrinol Metab. 2004 Aug;89(8):3979-82. doi: 10.1210/jc.2004-0406.
6
[Rickets following bone tumor].[骨肿瘤后的佝偻病]
Helv Paediatr Acta. 1959 Dec;14:554-65.
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Oncogenic osteomalacia--a complex dance of factors.致癌性骨软化症——多种因素的复杂交织
N Engl J Med. 2003 Apr 24;348(17):1705-8. doi: 10.1056/NEJMe030037.
8
Fibroblast growth factor 23 in oncogenic osteomalacia and X-linked hypophosphatemia.成骨细胞骨软化症和X连锁低磷血症中的成纤维细胞生长因子23
N Engl J Med. 2003 Apr 24;348(17):1656-63. doi: 10.1056/NEJMoa020881.
9
Increased circulatory level of biologically active full-length FGF-23 in patients with hypophosphatemic rickets/osteomalacia.低磷性佝偻病/骨软化症患者体内具有生物活性的全长成纤维细胞生长因子23(FGF-23)循环水平升高。
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10
Syndrome of inappropriate antidiuretic hormone associated with chemotherapy-induced tumour lysis in small-cell lung cancer: case report and literature review.小细胞肺癌化疗诱导肿瘤溶解综合征相关抗利尿激素分泌异常综合征:病例报告及文献复习
Ann Oncol. 2000 Aug;11(8):1061-5. doi: 10.1023/a:1008369932384.

双重副肿瘤综合征:小细胞肺癌相关的致癌性骨软化症及抗利尿激素分泌不当综合征:病例报告及文献复习

Dual paraneoplastic syndromes: small cell lung carcinoma-related oncogenic osteomalacia, and syndrome of inappropriate antidiuretic hormone secretion: report of a case and review of the literature.

作者信息

Tantisattamo Ekamol, Ng Roland C K

机构信息

Department of Medicine, John A. Burns School of Medicine, University of Hawai'i, Honolulu, HI 96813, USA.

出版信息

Hawaii Med J. 2011 Jul;70(7):139-43.

PMID:21886301
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3158371/
Abstract

Acquired isolated renal phosphate wasting associated with a tumor, known as oncogenic osteomalacia or tumor-induced osteomalacia, is a rare paraneoplastic syndrome caused by overproduction of fibroblast growth factor 23. Oncogenic osteomalacia is usually associated with benign mesenchymal tumors. Syndrome of inappropriate antidiuretic hormone secretion (SIADH), on the other hand, is a common paraneoplastic syndrome caused by small cell carcinoma (SCC). Concomitant oncogenic osteomalacia and SIADH associated with SCC is very rare with only 4 other cases reported in the literature. The authors report a case of small cell lung cancer (SCLC)-related renal wasting hypophosphatemia and concurrent SIADH, and review the literature reporting 9 other cases of SCC associated with oncogenic osteomalacia. Almost half of reported cases of renal phosphate wasting associated with SCC concomitantly presented with SIADH. These cases had initial serum phosphorus level lower and survival periods shorter than those without SIADH. This rare combination of a dual paraneoplastic syndrome and low serum phosphorus may be a poor prognostic sign. In addition, both renal phosphate wasting and SIADH usually occur in a short period of time before identification of SCC. Therefore, renal wasting hypophosphatemia with concomitant SIADH/hyponatremia should prompt a search for SCC rather than a benign mesenchymal tumor.

摘要

获得性孤立性肾性磷耗竭伴肿瘤,称为肿瘤性骨软化症或肿瘤诱导性骨软化症,是一种由成纤维细胞生长因子23过度产生引起的罕见副肿瘤综合征。肿瘤性骨软化症通常与良性间叶肿瘤相关。另一方面,抗利尿激素分泌不当综合征(SIADH)是一种由小细胞癌(SCC)引起的常见副肿瘤综合征。伴有SCC的肿瘤性骨软化症和SIADH非常罕见,文献中仅报道了另外4例。作者报告了1例与小细胞肺癌(SCLC)相关的肾性磷耗竭低磷血症并并发SIADH的病例,并回顾了文献中报道的另外9例与肿瘤性骨软化症相关的SCC病例。几乎一半与SCC相关的肾性磷耗竭报道病例同时伴有SIADH。这些病例的初始血清磷水平低于无SIADH的病例,生存期也更短。这种罕见的双重副肿瘤综合征与低血清磷的组合可能是预后不良的标志。此外,肾性磷耗竭和SIADH通常在SCC确诊前的短时间内出现。因此,伴有SIADH/低钠血症的肾性磷耗竭低磷血症应促使寻找SCC而非良性间叶肿瘤。