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BibTex RIS Kaynak Göster
Yıl 2023, Cilt: 9 Sayı: 1, 173 - 177, 04.01.2023
https://doi.org/10.18621/eurj.1022302

Öz

Kaynakça

  • 1. Young WF. Clinical presentation and diagnosis of pheochromocytoma. 2022. https://www.uptodate.com/contents/clinical-presentation-and-diagnosis-of-pheochromocytoma. Accessed date: February 21, 2022.
  • 2. Lenders JW, Eisenhofer G, Mannelli M, Pacak K. Phaeochromocytoma. Lancet 2005;366:665-75.
  • 3. Linet MS, Ries LA, Smith MA, Tarone RE, Devesa VV. Cancer surveillance series: recenttrends in childhood cancer incidence and mortality in the United States. J Natl Cancer Inst 1999; 91:1051-8.
  • 4. Bholah R, Bunchman TE. Review of pediatric pheochromocytoma and paraganglioma. Front Pediatr 2017;5:155.
  • 5. Wyszyńska T, Cichocka E, Wieteska-Klimczak A, Januszewicz P. A single pediatric center experience with 1025 children with hypertension. Acta Paediatr 1992;81:244-6.
  • 6. Barontini M, Levin G, Sanso G. Characteristics of pheochromocytoma in a 4- to 20-year-old population. Ann N Y Acad Sci 2006;1073:30-7.
  • 7. Waguespack SG, Rich T, Grubbs E, Ying AK, Perrier ND, Ayala-Ramirez M, et al. A current review of the etiology, diagnosis, andtreatment of pediatric pheochromocytoma and paraganglioma. J Clin Endocrinol Metab 2010;95:2023-37.
  • 8. Loosli N, Kohler BB, Pechere-Bertschi A, Karenovics W, Triponex F. Pheochromocytome et paragangliome: Que doit retenir le praticien? Rev Med Suisse 2014;10:1650-2.
  • 9. Ilias I, Meristoudis G, Notopoulos A. A probabilistic assessment of the diagnosis of paraganglioma/pheochromocytoma based on clinical criteria and biochemical/imaging findings. Hell J Nucl Med 2015;18:63-5.
  • 10. Gimenez-Roqueplo AP, Dahia PL, Robledo M. An update on thegenetics of paraganglioma, pheochromocytoma, and associated hereditary syndromes. Horm Metab Res 2012;44:328-33.
  • 11. Molaei A, Abarzadeh-Bairami V, Sadat-Ebrahimi S-R. A case of pheochromocytoma presenting with cardiac manifestation: case report. BMC Pediatr 2020;20:299.
  • 12. Beltsevich DG, Kuznetsov NS, Kazaryan AM, Lysenko MA. Pheochromocytoma surgery: epidemiologic peculiarities in children. World J Surg 2004;28:592-6.
  • 13. Pham TH, Moir C, Thompson GB, Zarroug AE, Hamner CE, Farley D, et al. Pheochromocytoma and paraganglioma in children: a review of medical and surgical management at a tertiary care center. Pediatrics 2006;18:1109-17.
  • 14. van der Zee PA, de Boer A. Pheochromocytoma: a review on preoperative treatment with phenoxybenzamine or doxazosin. Neth J Med 2014;72:190-201.

Paraganglioma admitting with stage-4 hypertensive retinopathy

Yıl 2023, Cilt: 9 Sayı: 1, 173 - 177, 04.01.2023
https://doi.org/10.18621/eurj.1022302

Öz

Paragangliomas and pheochromocytomas are rare tumors originating in chromaffin cells which are predominantly located in adrenal glands. This tumor is generally bilateral and much more rarely seen in pediatric patients. Sustained or paroxysmal hypertension is the most frequent sign of paragangliomas /pheochromocytoma. Here, we present a 15-year-old patient diagnosed with the complaint of blurred vision.

Kaynakça

  • 1. Young WF. Clinical presentation and diagnosis of pheochromocytoma. 2022. https://www.uptodate.com/contents/clinical-presentation-and-diagnosis-of-pheochromocytoma. Accessed date: February 21, 2022.
  • 2. Lenders JW, Eisenhofer G, Mannelli M, Pacak K. Phaeochromocytoma. Lancet 2005;366:665-75.
  • 3. Linet MS, Ries LA, Smith MA, Tarone RE, Devesa VV. Cancer surveillance series: recenttrends in childhood cancer incidence and mortality in the United States. J Natl Cancer Inst 1999; 91:1051-8.
  • 4. Bholah R, Bunchman TE. Review of pediatric pheochromocytoma and paraganglioma. Front Pediatr 2017;5:155.
  • 5. Wyszyńska T, Cichocka E, Wieteska-Klimczak A, Januszewicz P. A single pediatric center experience with 1025 children with hypertension. Acta Paediatr 1992;81:244-6.
  • 6. Barontini M, Levin G, Sanso G. Characteristics of pheochromocytoma in a 4- to 20-year-old population. Ann N Y Acad Sci 2006;1073:30-7.
  • 7. Waguespack SG, Rich T, Grubbs E, Ying AK, Perrier ND, Ayala-Ramirez M, et al. A current review of the etiology, diagnosis, andtreatment of pediatric pheochromocytoma and paraganglioma. J Clin Endocrinol Metab 2010;95:2023-37.
  • 8. Loosli N, Kohler BB, Pechere-Bertschi A, Karenovics W, Triponex F. Pheochromocytome et paragangliome: Que doit retenir le praticien? Rev Med Suisse 2014;10:1650-2.
  • 9. Ilias I, Meristoudis G, Notopoulos A. A probabilistic assessment of the diagnosis of paraganglioma/pheochromocytoma based on clinical criteria and biochemical/imaging findings. Hell J Nucl Med 2015;18:63-5.
  • 10. Gimenez-Roqueplo AP, Dahia PL, Robledo M. An update on thegenetics of paraganglioma, pheochromocytoma, and associated hereditary syndromes. Horm Metab Res 2012;44:328-33.
  • 11. Molaei A, Abarzadeh-Bairami V, Sadat-Ebrahimi S-R. A case of pheochromocytoma presenting with cardiac manifestation: case report. BMC Pediatr 2020;20:299.
  • 12. Beltsevich DG, Kuznetsov NS, Kazaryan AM, Lysenko MA. Pheochromocytoma surgery: epidemiologic peculiarities in children. World J Surg 2004;28:592-6.
  • 13. Pham TH, Moir C, Thompson GB, Zarroug AE, Hamner CE, Farley D, et al. Pheochromocytoma and paraganglioma in children: a review of medical and surgical management at a tertiary care center. Pediatrics 2006;18:1109-17.
  • 14. van der Zee PA, de Boer A. Pheochromocytoma: a review on preoperative treatment with phenoxybenzamine or doxazosin. Neth J Med 2014;72:190-201.
Toplam 14 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Çocuk Sağlığı ve Hastalıkları
Bölüm Case Report
Yazarlar

İsa Yılmaz 0000-0001-8654-9173

Fatma Özcan Sıkı 0000-0002-4461-3461

Mehmet Öztürk 0000-0001-5585-1476

Fuat Buğrul 0000-0002-2276-4410

Zeliha Esin Çelik 0000-0002-3220-7845

Şükrü  Arslan 0000-0001-5632-8273

Yayımlanma Tarihi 4 Ocak 2023
Gönderilme Tarihi 11 Kasım 2021
Kabul Tarihi 21 Şubat 2022
Yayımlandığı Sayı Yıl 2023 Cilt: 9 Sayı: 1

Kaynak Göster

AMA Yılmaz İ, Özcan Sıkı F, Öztürk M, Buğrul F, Çelik ZE, Arslan Ş. Paraganglioma admitting with stage-4 hypertensive retinopathy. Eur Res J. Ocak 2023;9(1):173-177. doi:10.18621/eurj.1022302

e-ISSN: 2149-3189 


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