Startseite Medizin Rare and curable renin-mediated hypertension: a series of six cases and a literature review
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Rare and curable renin-mediated hypertension: a series of six cases and a literature review

  • Wei-Jun Gu , Lin-Xi Zhang , Nan Jin , Jian-Ming Ba EMAIL logo , Jun Dong , Dian-Jun Wang , Jie Li , Xian-Ling Wang , Guo-Qing Yang , Zhao-Hui Lu , Jing-Tao Dou , Ju-Ming Lu und Yi-Ming Mu EMAIL logo
Veröffentlicht/Copyright: 23. Oktober 2015

Abstract

Background: Reninoma is an extremely rare renal tumor characterized by excessive renin secretion causing secondary hypertension and hypokalemia. Reninoma is a benign and highly manageable lesion if it is discovered early and removed surgically.

Methods: We report six cases of reninoma and provide a literature review on this rare disease, highlighting the diagnostic evaluation and follow-up of each patient.

Results and conclusions: Reninoma should be considered in young adults with elevated renin activity and refractory hypertension. Imaging studies and selective venous catheterization are often helpful in identifying the lesion. In most cases of reninoma presenting with renin-mediated hypertension, conservative surgical treatment should be considered to remove the small, superficial lesion.


Corresponding authors: Jian-Ming Ba, MD, PhD, Department of Endocrinology, Chinese PLA General Hospital, Beijing 100853, P.R. China, Phone: +86-10-5549 9102, Fax: +86-10-6816 8631, E-mail: ; and Yi-Ming Mu, MD, PhD, Department of Endocrinology, Chinese PLA General Hospital, Beijing 100853, P.R. China, Phone: +86-10-5549 9001, Fax: +86-10-6816 8917, E-mail:
aWei-Jun Gu and Lin-Xi Zhang: These authors contributed equally to this work.

Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

Research funding: None declared.

Employment or leadership: None declared.

Honorarium: None declared.

Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

References

1. Saito T, Fukamizu A, Okada K, Ishikawa S, Iwamoto Y, et al. Ectopic production of renin by ileal carcinoma. Endocrinol Jpn 1989;36:117–24.10.1507/endocrj1954.36.117Suche in Google Scholar

2. Pursell RN, Quinlan PM. Secondary hypertension due to a renin-producing teratoma. Am J Hypertens 2003;16:592–5.10.1016/S0895-7061(03)00865-3Suche in Google Scholar

3. Wong L, Hsu TH, Perlroth MG, Hofmann LV, Haynes CM, et al. Reninoma: case report and literature review. J Hypertens 2008;26:368–73.10.1097/HJH.0b013e3282f283f3Suche in Google Scholar

4. Corvol P, Ménard J. Renin inhibition: immunological procedures and renin inhibitor peptides. Kidney Int 1988;26(Supp l):S73–9.Suche in Google Scholar

5. Lin SY, Liu WY, Chen WC, Chen RH. Secondary hypertension due to a renin-secreting juxtaglomerular cell tumor. J Formos Med Assoc 2010;109:237–40.10.1016/S0929-6646(10)60047-2Suche in Google Scholar

6. Gottardo F, Cesari M, Morra A, Gardiman M, Fassina A, et al. A kidney tumor in an adolescent with severe hypertension and hypokalemia: an uncommon case – case report and review of the literature on reninoma. Urol Int 2010;85:121–4.10.1159/000314339Suche in Google Scholar

7. Mete UK, Niranjan J, Kusum J, Rajesh LS, Goswami AK, et al. Reninoma treated with nephron-sparing surgery. Urology 2003;61:1259iii-v.10.1016/S0090-4295(03)00104-3Suche in Google Scholar

8. Sakata R, Shimoyamada H, Yanagisawa M, Murakami T, Makiyama K, et al. Nonfunctioning juxtaglomerular cell tumor. Case Rep Pathol 2013;2013:973865.10.1155/2013/973865Suche in Google Scholar PubMed PubMed Central

9. Endoh Y, Motoyama T, Hayami S, Kihara I. Juxtaglomerular cell tumor of the kidney: report of a nonfunctioning variant. Pathol Int 1997;47:393–6.10.1111/j.1440-1827.1997.tb04513.xSuche in Google Scholar PubMed

10. Henderson NL, Mason RC. Juxtaglomerular cell tumor in pregnancy. Obstet Gynecol 2001;98:943–5.Suche in Google Scholar

11. Liborio AB, Marques Fde O, Testagrossa L, Leite CA, Leitao AA, et al. Malignant hypertension with intestinal ischemia secondary to juxtaglomerular cell tumor. Am J Kidney Dis 2005;46:957–61.10.1053/j.ajkd.2005.07.032Suche in Google Scholar PubMed

12. Kim HJ, Kim CH, Choi YJ, Ayala AG, Amirikachi M, et al. Juxtaglomerular cell tumor of kidney with CD34 and CD117 immunoreactivity: report of 5 cases. Arch Pathol Lab Med 2006;130:707–11.10.5858/2006-130-707-JCTOKWSuche in Google Scholar PubMed

13. Brand G, Vandongen R, Beilin LJ, Matz L. Juxtaglomerular tumour: diagnostic renal vein renin measurements obscured by chronic captopril therapy. Aust NZ J Med 1985;15:755–7.Suche in Google Scholar

14. Corvol P, Pinet F, Plouin PF, Bruneval P, Menard J. Renin-secreting tumors. Endocrinol Metab Clin North Am 1994;23:255–70.10.1016/S0889-8529(18)30096-3Suche in Google Scholar

15. Hanna W, Tepperman B, Logan AG, Robinette MA, Colapinto R, et al. Juxtaglomerular cell tumour (reninoma) with paroxysmal hypertension. Can Med Assoc J 1979;120:957–9.Suche in Google Scholar

16. Duan X, Bruneval P, Hammadeh R, Fresco R, Eble JN, et al. Meastatic juxtaglomerular cell tumor in a 52-year-old man. Am J Surg Pathol 2004;28:1098–102.10.1097/01.pas.0000126722.29212.a7Suche in Google Scholar PubMed

17. Beaudoin J, Périgny M, Têtu B, Lebel M. A patient with a juxtaglomerular cell tumor with histological vascular invasion. Nat Clin Pract Nephrol 2008;4:458–62.10.1038/ncpneph0890Suche in Google Scholar PubMed

Received: 2015-1-15
Accepted: 2015-8-27
Published Online: 2015-10-23
Published in Print: 2016-2-1

©2016 by De Gruyter

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