| Literature DB >> 24293913 |
Mehdi Soufi1, Mohammed K Lahlou, Said Benamr, Rahal Massrouri, Jalil Mdaghri, Abdelhamid Essadel, Mohammadine El Hamid, Ahmed Taghy, Abdelatif Settaf, Bouziane Chad.
Abstract
Cystic malignant pheochromocytomas are uncommon. Differing from solid pheochromocytomas, which produce catecholamines and present adrenergic syndrome, cystic pheochromocytomas, may not produce these. Preoperative diagnosis may be difficult. Ct scan is useful for preoperative management. In this report, we describe a case of a giant malignant cystic pheochromocytoma in a young woman (17 years old) which presented as giant abdominal mass. The malignancy was confirmed by the presence of liver metastasis. Two years after curative resection, the patient is in good health with no recurrence.Entities:
Keywords: Adrenalectomy; Chemotherapy; Malignant Pheochromocytoma; Neuroendocrine tumors
Year: 2012 PMID: 24293913 PMCID: PMC3538001 DOI: 10.1007/s12262-012-0719-x
Source DB: PubMed Journal: Indian J Surg ISSN: 0973-9793 Impact factor: 0.656