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Hipofisitis granulomatosa
J. Sala, J.M. Izquierdo, E. Bráñez
Departamento de Cirugía (Neurocirugía) y de A. Patológica. Facultad de Medicina y Centro Médico de Asturias. Oviedo
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        "resumen" => "<p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">We report a case of granulomatous hypophysitis in a 38 year old woman who suffered cephalea and dyplopia&#44; caused by left abducens palsy&#46; No relevant endocrine alteration was observed&#46;</p><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">Plain x-ray films and C&#46;T&#46; were normal&#44; but M&#46;R&#46;I&#46; disclosed an enlarged sellar content&#44; what was supossed to be a pituitary tumor&#46;</p><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Transphenoidal surgical exploration of the sella revealed a hypertrophic hypophysis&#44; without adenomatous tissue&#46;</p><p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">Histopathological analysis of the taken samples showed definite signs of granulomatous hypophysitis&#46;</p><p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">After two months of corticoid treatment&#44; dyplopia disappeared&#46;</p>"
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