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>Journals >Cirujano General >Year 2005, Issue 4


Delgadillo TGH, González RF, Fenig RJ, Velázquez GA, Galindo ML, Bevia PF
Experience in the surgical management of pheochromocytoma
Cir Gen 2005; 27 (4)

Language: Español
References: 13
Page: 301-303
PDF: 4. Kb.


Full text




ABSTRACT

Objective:To know the frequency of presentation of pheochromocytoma at the Specialty Hospital of the Centro Medico Nacional “La Raza”, IMSS, in Mexico City.
Setting:Third level health care institution.
Design:Retrospective, descriptive, transversal study.
Patients and methods:We analyzed the clinical and histological records of all patients with a diagnosis of pheochromocytoma, with a suprarenal location, from January 1989 to December 2000.
Results:A total of 31 patients with pheochromocytoma, suprarenal location, were attended; 87% were women and 13% were men. Average age of presentation was 31 years: The clinical symptoms were characterized by headache, hard to control arterial hypertension, and diaphoresis in 97% of the cases. Diagnosis was reached by determining the presence of catecholamines in a 24-hours urine sample and through an abdominal CAT scan. Affection of the right suprarenal gland was more frequent with 88% of the cases, the left with 9%, and in 3% the affection was bilateral. The most frequent complication was postoperative bleeding in 19% and pancreatitis in one patient. Mortality was of 3%. Histologically, the pathology was benign in 97% and malignant in 3%.
Conclusions:Affection of the suprarenal gland by a pheochromocytoma is a rare pathology in our milieu, it affects more frequently women; a hard to control hypertension is the most frequent sign in young patients, presenting as headache.


Key words: Pheochromocytoma, hypertension, suprarenal gland.


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>Journals >Cirujano General >Year 2005, Issue 4
 

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