Literature DB >> 16438086

An adult adrenal neuroblastoma: a case report.

H Genc1, M Haciyanli, S G Haciyanli, F Gelal, A Avci Uçarsoy, F Dag.   

Abstract

Neuroblastoma of the adrenal gland is an extremely rare tumour in adulthood although it is one of the most common malignancies in childhood. In this report, we present a 52-year-old man who had a left adrenal mass on preoperative imaging. On laboratory, slightly elevated catecholamine metabolites were detected in the urine that was collected over 24 hours. He was operated and the mass was resected in en-block manner along with the regional lymph nodes. The histopathological examination of the specimen revealed the diagnosis of neuroblastoma. He had no metastatic disease at the time of diagnosis and received chemotherapy after the operation. However, the prognosis was poor and he died 10 months after the operation. Although neuroblastoma of adrenal gland is rare in adulthood, it should be considered in the differential diagnosis for patients with adrenal masses.

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Year:  2005        PMID: 16438086     DOI: 10.1080/00015458.2005.11679803

Source DB:  PubMed          Journal:  Acta Chir Belg        ISSN: 0001-5458            Impact factor:   1.090


  1 in total

1.  Adrenal Neuroblastoma Producing Catecholamines Diagnosed in Adults: Case Report.

Authors:  Guillermo Edinson Guzman Gómez; Maria Alejandra Urbano; Veline Martínez
Journal:  Case Rep Oncol       Date:  2022-07-07
  1 in total

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