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A case report of subclinical hypercortisolism due to adrenal incidentaloma complicated by myasthenia gravis after adrenalectomy.
Petramala, Luigi; Marinelli, Cristiano; Giallonardo, Anna Teresa; Concistrè, Antonio; Lucia, Piernatale; Venuta, Federico; Cerbelli, Bruna; Ciardi, Antonio; De Toma, Giorgio; Letizia, Claudio.
Afiliação
  • Petramala L; Department of Internal Medicine and Medical Specialties, La Sapienza University, Rome - Italy.
  • Marinelli C; Department of Internal Medicine and Medical Specialties, La Sapienza University, Rome - Italy.
  • Giallonardo AT; Department of Neurological Sciences, La Sapienza University, Rome - Italy.
  • Concistrè A; Department of Internal Medicine and Medical Specialties, La Sapienza University, Rome - Italy.
  • Lucia P; Department of Internal Medicine and Medical Specialties, La Sapienza University, Rome - Italy.
  • Venuta F; Department of Thoracic Surgery, Policlinico Umberto I, La Sapienza University, Rome - Italy.
  • Cerbelli B; Department of Surgery "Pietro Valdoni", La Sapienza University, Rome - Italy.
  • Ciardi A; Department of Surgery "Pietro Valdoni", La Sapienza University, Rome - Italy.
  • De Toma G; Department of Surgery "Pietro Valdoni", La Sapienza University, Rome - Italy.
  • Letizia C; Department of Internal Medicine and Medical Specialties, La Sapienza University, Rome - Italy.
Tumori ; 102(Suppl. 2)2016 Nov 11.
Article em En | MEDLINE | ID: mdl-27103206
ABSTRACT
A 62-year-old woman was admitted for evaluation of an incidentally discovered adrenal mass and hypertension. CT scan revealed a 7 cm mass in the right adrenal gland. After careful examination, the patient was diagnosed with subclinical hypercortisolism (SH). Adrenalectomy was performed. Histopathological examination showed an adrenocortical adenoma. Symptoms and signs of myasthenia gravis appeared 5 months later. CT of the chest showed a solid tissue mass in the mediastinum. The patient underwent a sternotomy with excision of the tumor, which histologically proved to be a type 2B thymoma. We describe a rare case of SH due to an incidentally discovered adrenocortical adenoma in a patient who manifested myasthenia gravis after surgical remission of the cortisol excess.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias das Glândulas Suprarrenais / Adrenalectomia / Miastenia Gravis Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias das Glândulas Suprarrenais / Adrenalectomia / Miastenia Gravis Idioma: En Ano de publicação: 2016 Tipo de documento: Article