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Ghazizadeh, F., Ebadi, M., Alavi, S., Arzanian, M., Shamsian, B. and Jadali, F. (2013) Adrenocortical Carcinoma Presenting with Heterosexual Pseudoprecocious Puberty Shortly after Birth: Case Report and Review. Ecancermedicalscience, 7, 289.

has been cited by the following article:

• TITLE: Cushing Syndrome Revealing an Adrenocortical Carcinoma

  AUTHORS: Bintou Sanogo, Senkaye-Lagom Aimée Kissou, Zakari Nikiema, Makoura Barro, Djingri Lankouandé, Boubacar Nacro

  KEYWORDS: Cushing Syndrome, Adrenocortical Carcinoma, Child

  JOURNAL NAME: Open Journal of Pediatrics, Vol.8 No.2, April 18, 2018

  ABSTRACT: Adrenocortical carcinoma is a malignant tumor of the adrenal gland, very rare in pediatric pathology. Authors presented a pediatric case of adrenocortical carcinoma which showed neurology symptoms at 1st visit and Cushing syndrome secondarily. The patient received a ketoconazole-based treatment. The outcome was fatal before the surgical excision of the tumor, because of delayed diagnosis. Early diagnosis and multidisciplinary management of adrenocortical carcinoma could improve the prognosis in children.