Anaesthesic Problems in Bilateral Pheochromocytoma
نویسندگان
چکیده
منابع مشابه
Bilateral stellate neuroretinitis revealing a pheochromocytoma
Neuroretinitis (NR) is an inflammatory disorder characterized by optic disc edema and subsequent formation of a macular star. We present a case of a 33 year old woman patient admitted for a progressive bilateral visual loss since two weeks. Fundus examination showed bilateral stellate neuroretinitis. Physical examination revealed a malignant hypertension of 210/150 mmHg. Magnetic resonance imag...
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BACKGROUND Pheochromocytoma is a disease where catecholamines are secreted. If pheochromocytoma occurs during pregnancy, it can be difficult to diagnose because it is similar to pregnancy-induced hypertension. Furthermore, bilateral pheochromocytoma during pregnancy is even rarer than unilateral pheochromocytoma. CASE PRESENTATION A 32-year-old primigravida, who was 12 weeks' pregnant, was aw...
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summary: pheochromocytoma is an adrenal tumor characterized by symptoms of hypertension, headache, increased sweating, and tachycardia .in one third of patients, the tumor is discovered incidentally during radiological evaluation of the abdomen. in this article a case of bilateral pheochromocytoma is reported. the patient, a twelve years old boy, referred with complaints of headache, flushing, ...
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conclusions we described successful perioperative management of a child who underwent bilateral laparoscopic cortical sparing adrenalectomy and a repeated surgery for the residual tumor removal. case presentation the child might present with a spectrum of clinical manifestation including hypertension, headache, visual disturbances, and behavioral problems. a meticulous preoperative preparation ...
متن کاملLaparoscopic Cortical Sparing Adrenalectomy for Pediatric Bilateral Pheochromocytoma: Anesthetic Management
INTRODUCTION Pheochromocytoma is a catecholamine-secreting tumor, which is seen rarely in children. These tumors predominantly secrete norepinephrine and epinephrine. They might be familial and associated with hereditary tumors such as Von Hippel-Lindau syndrome and multiple endocrine neoplasia type II. CASE PRESENTATION The child might present with a spectrum of clinical manifestation includ...
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ژورنال
عنوان ژورنال: The Journal of Tepecik Education and Research Hospital
سال: 1998
ISSN: 1305-7073
DOI: 10.5222/terh.1998.80947