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1.
Langenbecks Arch Surg ; 392(6): 663-70, 2007 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-17375321

RESUMO

BACKGROUND: The persistent hyperinsulinemic hypoglycemia is characterized by clinical symptoms that occur when the blood glucose levels drop below the normal range. Two pathological situations cause this clinical problem: The presence of a tumor of the pancreas secreting excessive amounts of insulin, known as insulinoma, and congenital beta-cell hyperplasia in the pancreas in children and noninsulinoma pancreatogenic hypoglycemia syndrome in adults. PATIENTS AND METHODS: Clinical characteristic and surgical outcome of a group of 20 patients operated on for this hypoglycemic syndrome; 18 for insulinoma and two for nesidioblastosis in children was studied. RESULTS: eight of the insulinomas were in the head of the pancreas, two in the body, and the remaining eight in the tail. The surgical technique was enucleation in nine cases, local resection in one case because of suspicious malignancy, and distal pancreatectomy in eight cases. Both children with nesidioblastosis underwent 85% pancreatectomy with splenic preservation. There was no mortality in the study, but three patients developed a low-volume pancreatic fistula after head enucleation. CONCLUSIONS: Negative results in diagnostic localization together with the small size of the insulinoma represent a poor combination for successful surgery. The intraoperative ultrasonography is the method of choice for the identification of the tumor, as it is able to identify nonpalpable lesions.


Assuntos
Hiperinsulinismo/cirurgia , Insulinoma/cirurgia , Neoplasia Endócrina Múltipla Tipo 1/cirurgia , Nesidioblastose/cirurgia , Neoplasias Pancreáticas/cirurgia , Adulto , Idoso , Hiperinsulinismo Congênito/diagnóstico , Hiperinsulinismo Congênito/cirurgia , Feminino , Humanos , Hiperinsulinismo/diagnóstico , Lactente , Insulinoma/diagnóstico , Laparoscopia/métodos , Masculino , Pessoa de Meia-Idade , Neoplasia Endócrina Múltipla Tipo 1/diagnóstico , Nesidioblastose/diagnóstico , Pancreatectomia/métodos , Neoplasias Pancreáticas/diagnóstico , Complicações Pós-Operatórias/etiologia
2.
J Clin Endocrinol Metab ; 90(1): 316-22, 2005 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-15507518

RESUMO

Metabolic alterations such as insulin resistance are thought to underlie the endothelial dysfunction and low grade inflammation found in morbid obesity. Twenty-six morbidly obese patients, aged 39.0 +/- 10.0 (mean +/- sd), were evaluated before and 4.2 +/- 0.8 months after bariatric surgery. A marked increment in the insulin sensitivity index (S(I)) and the endothelium-dependent vasodilatory response in a dorsal hand vein was observed after weight loss following bariatric surgery. Circulating levels of E-selectin, P-selectin, plasminogen activator inhibitor-1, and von Willebrand factor, which were higher than those in the control group, decreased significantly after surgery. Plasma vascular cell adhesion molecule-1, angiotensin-converting enzyme, intercellular adhesion molecule-1, thrombomodulin, and plasma and intraplatelet cGMP levels did not change after weight loss. All inflammatory markers were higher in morbidly obese patients. After surgery, C- reactive protein and sialic acid diminished, whereas circulating levels of IL-6, TNF-alpha, and its soluble receptors did not. Positive correlations were found between changes in adiposity and S(I) and changes in C-reactive protein and between changes in sialic acid and changes in endothelial function. In conclusion, a marked improvement in S(I), endothelial function, and low grade inflammation was observed in the weight-losing, morbidly obese patients after bariatric surgery. S(I) and adiposity appear to play roles in obesity-related, low grade inflammation that contribute to the endothelial dysfunction observed in morbid obesity.


Assuntos
Peso Corporal , Endotélio/fisiologia , Derivação Gástrica , Inflamação/etiologia , Resistência à Insulina , Obesidade Mórbida/cirurgia , Adulto , Feminino , Humanos , Interleucina-6/fisiologia , Masculino , Pessoa de Meia-Idade , Obesidade Mórbida/fisiopatologia , Fator de Necrose Tumoral alfa/fisiologia , Molécula 1 de Adesão de Célula Vascular/sangue
3.
Pain ; 47(3): 341-344, 1991 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-1664509

RESUMO

We report a patient with acromegaly who had severe, intractable headache unrelated to tumor size which dramatically resolved with the somatostatin analog octreotide. The analgesic effects of octreotide were neither related to significant inhibition of growth hormone nor influenced by naloxone. Our data suggest that octreotide should be considered in patients with intractable headache associated with pituitary adenomas. Mechanisms other than tumor size or interaction with the opioid system, such as non-opioid algesic peptide secretion, may be the explanation for severe head pain in some pituitary adenomas.


Assuntos
Acromegalia/complicações , Cefaleia/tratamento farmacológico , Octreotida/uso terapêutico , Adenoma/complicações , Adulto , Hormônio do Crescimento/metabolismo , Cefaleia/etiologia , Cefaleia/fisiopatologia , Humanos , Masculino , Naloxona/farmacologia , Dor Intratável/tratamento farmacológico , Dor Intratável/fisiopatologia , Neoplasias Hipofisárias/complicações , Receptores Opioides/efeitos dos fármacos
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