Pheochromocytoma is a rarely seen neuroendocrine tumor that causes hypertension, tachycardia, sweating, palpitations, headache and anxiety. Excessive cathecolamin release can occur during surgical mani¬pulation and induction of general anesthesia. Particularly this release can increase during resection of tumor (1). In these clients, a meticu¬lous preoperative preperation and perioperative close monitorisation is important (2). It is possible to come up with these patients which are not diagnosed before, during surgeries other than surrenal surgery. Int¬raoperative malignant hypertension should bring pheochromacytoma in minds and postoperative tests should be done for diagnosis. In this report we aimed to share a case which had malignant hypertansive cri¬sis during ortophedic surgery and diagnosed as a pheochromocytoma postoperatively.
Konular | Sağlık Kurumları Yönetimi |
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Bölüm | Olgu Sunumu |
Yazarlar | |
Yayımlanma Tarihi | 26 Aralık 2016 |
Kabul Tarihi | 3 Ocak 2016 |
Yayımlandığı Sayı | Yıl 2016 Cilt: 6 Sayı: 4 |