Table of Contents Author Guidelines Submit a Manuscript
Case Reports in Surgery
Volume 2015, Article ID 375416, 5 pages
http://dx.doi.org/10.1155/2015/375416
Case Report

A Pleural Solitary Fibrous Tumor, Multiple Gastrointestinal Stromal Tumors, Moyamoya Disease, and Hyperparathyroidism in a Patient Associated with NF1

1Department of Thoracic Surgery, Yao Municipal Hospital, Yao City, Osaka 581-0069, Japan
2Department of Gastroenterological Surgery, Yao Municipal Hospital, Yao City, Osaka 581-0069, Japan
3Department of Pathology, Yao Municipal Hospital, Yao City, Osaka 581-0069, Japan
4Department of Breast and Endocrine Surgery, Osaka University, Osaka 565-0871, Japan

Received 28 June 2015; Revised 27 August 2015; Accepted 31 August 2015

Academic Editor: Geeta Lal

Copyright © 2015 Yoko Yamamoto et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. S. A. Rasmussen and J. M. Friedman, “NF1 gene and neurofibromatosis,” American Journal of Epidemiology, vol. 151, no. 1, pp. 33–40, 2000. View at Publisher · View at Google Scholar · View at Scopus
  2. J. M. Friedman, J. Arbiter, J. A. Epstein et al., “Cardiovascular disease in neurofibromatosis 1: report of the NF1 Cardiovascular Task Force,” Genetics in Medicine, vol. 4, no. 3, pp. 105–111, 2002. View at Publisher · View at Google Scholar · View at Scopus
  3. C. E. Fuller and G. T. Williams, “Gastrointestinal manifestations of type 1 neurofibromatosis (von Recklinghausen's disease),” Histopathology, vol. 19, no. 1, pp. 1–11, 1991. View at Publisher · View at Google Scholar · View at Scopus
  4. M. Miettinen, J. F. Fetsch, L. H. Sobin, and J. Lasota, “Gastrointestinal stromal tumors in patients with neurofibromatosis 1: a clinicopathologic and molecular genetic study of 45 cases,” American Journal of Surgical Pathology, vol. 30, no. 1, pp. 90–96, 2006. View at Publisher · View at Google Scholar · View at Scopus
  5. V. B. Shidham, M. Chivukula, D. Gupta, R. N. Rao, and R. Komorowski, “Immunohistochemical comparison of gastrointestinal stromal tumor and solitary fibrous tumor,” Archives of Pathology and Laboratory Medicine, vol. 126, no. 10, pp. 1189–1192, 2002. View at Google Scholar · View at Scopus
  6. K. Hirashima, H. Takamori, M. Hirota et al., “Multiple gastrointestinal stromal tumors in neurofibromatosis type 1: report of a case,” Surgery Today, vol. 39, no. 11, pp. 979–983, 2009. View at Publisher · View at Google Scholar · View at Scopus
  7. J. A. Giuly, R. Picand, D. Giuly, B. Monges, and R. Nguyen-Cat, “Von Recklinghausen disease and gastrointestinal stromal tumors,” American Journal of Surgery, vol. 185, no. 1, pp. 86–87, 2003. View at Publisher · View at Google Scholar · View at Scopus
  8. D. M. England, L. Hochholer, and M. J. McCarthy, “Localized benign and malignant fibrous tumors of pleura. A clinicopathologic review of 223 cases,” The American Journal of Surgical Pathology, vol. 13, no. 8, pp. 640–658, 1989. View at Publisher · View at Google Scholar
  9. R. Vogels, M. Vlenterie, Y. Versleijen-Jonkers et al., “Solitary fibrous tumor—clinicopathologic, immunohistochemical and molecular analysis of 28 cases,” Diagnostic Pathology, vol. 9, article 224, 2014. View at Publisher · View at Google Scholar
  10. M. de Perrot, A.-M. Kurt, J. H. Robert, B. Borisch, and A. Spiliopoulos, “Clinical behavior of solitary fibrous tumors of the pleura,” Annals of Thoracic Surgery, vol. 67, no. 5, pp. 1456–1459, 1999. View at Publisher · View at Google Scholar · View at Scopus
  11. G. Conzo, E. Tartaglia, C. Gambardella et al., “Suprarenal solitary fibrous tumor associated with a NF1 gene mutation mimicking a kidney neoplasm: implications for surgical management,” World Journal of Surgical Oncology, vol. 12, article 87, 2014. View at Publisher · View at Google Scholar · View at Scopus
  12. L. C. Cunningham, J.-G. Yu, K. Shilo et al., “Thymoma and parathyroid adenoma: false-positive imaging and intriguing laboratory test results,” JAMA Otolaryngology—Head and Neck Surgery, vol. 140, no. 4, pp. 369–373, 2014. View at Publisher · View at Google Scholar · View at Scopus
  13. E. Vargiami, E. Sapountzi, D. Samakovitis et al., “Moyamoya syndrome and neurofibromatosis type 1,” Italian Journal of Pediatrics, vol. 40, article 59, 2014. View at Publisher · View at Google Scholar · View at Scopus
  14. T. Yamauchi, M. Tada, K. Houkin et al., “Linkage of familial moyamoya disease (spontaneous occlusion of the circle of Willis) to chromosome 17q25,” Stroke, vol. 31, pp. 930–935, 2000. View at Publisher · View at Google Scholar · View at Scopus
  15. D. Daly, M. Kaye, and R. L. Estrada, “Neurofibromatosis and hyperparathyroidism: a new syndrome?” Canadian Medical Association Journal, vol. 103, no. 3, pp. 258–259, 1970. View at Google Scholar · View at Scopus
  16. E. Gkaliagkousi, Z. Erlic, K. Petidis et al., “Neurofibromatosis type 1: should we screen for other genetic syndromes? A case report of co-existence with multiple endocrine neoplasia 2A,” European Journal of Clinical Investigation, vol. 39, no. 9, pp. 828–832, 2009. View at Publisher · View at Google Scholar · View at Scopus
  17. A. E. Altinova, F. Toruner, A. R. Cimen et al., “The association of neurofibromatosis, bilateral pheochromocytoma and primary hyperparathyroidism,” Experimental and Clinical Endocrinology and Diabetes, vol. 115, no. 7, pp. 468–470, 2007. View at Publisher · View at Google Scholar · View at Scopus