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Peripheral neuroblastic tumor of the kidney: case report and review of literature.
Moscheo, Carla; Campari, Alessandro; Podda, Marta Giorgia; Riccipetitoni, Giovanna; Collini, Paola; Renne, Salvatore Lorenzo; Vella, Claudio; Napolitano, Marcello; Luksch, Roberto.
Affiliation
  • Moscheo C; 1 Pediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
  • Campari A; 2 Current affiliation: Neuro-Oncology Unit, Department of Pediatric Oncology, Meyer Children's University Hospital, Florence, Italy.
  • Podda MG; 3 Pediatric Radiology Department, V. Buzzi Children's Hospital, Milan, Italy.
  • Riccipetitoni G; 1 Pediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
  • Collini P; 4 Pediatric Surgery, Children's Hospital "V. Buzzi," University of Milan, Milan, Italy.
  • Renne SL; 5 Soft Tissue and Bone Pathology, Histopathology, and Pediatric Pathology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
  • Vella C; 5 Soft Tissue and Bone Pathology, Histopathology, and Pediatric Pathology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
  • Napolitano M; 4 Pediatric Surgery, Children's Hospital "V. Buzzi," University of Milan, Milan, Italy.
  • Luksch R; 3 Pediatric Radiology Department, V. Buzzi Children's Hospital, Milan, Italy.
Tumori ; 104(6): NP34-NP37, 2018 Dec.
Article in En | MEDLINE | ID: mdl-30021475
ABSTRACT

INTRODUCTION:

Peripheral neuroblastic tumors (PNTs) account for 8%-10% of all pediatric tumors. Adrenal glands and sympathetic ganglia are the commonest site of tumor growth. In the clinicopathologic spectrum of PNTs, neuroblastoma and ganglioneuroma are the most primitive and the most mature tumor form, while ganglioneuroblastoma represents an intermediate state of maturation. Surgical resection is the therapy of choice in localized disease, but can lead to serious complications when performed in the presence of certain imaging-defined risk factors. CASE PRESENTATION We present a rare case of primary intrarenal ganglioneuroblastoma diagnosed in a teenager who underwent conservative surgery and, despite this, developed upper pole renal ischemia without loss of parenchymal function.

CONCLUSION:

We underline the complex management of these extremely rare cases of neuroblastic tumors, which require a dedicated multidisciplinary team.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Peripheral Nervous System Neoplasms / Ganglioneuroblastoma / Kidney Neoplasms / Neuroblastoma Type of study: Risk_factors_studies Limits: Adolescent / Female / Humans Language: En Journal: Tumori Year: 2018 Document type: Article Affiliation country: Italy

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Peripheral Nervous System Neoplasms / Ganglioneuroblastoma / Kidney Neoplasms / Neuroblastoma Type of study: Risk_factors_studies Limits: Adolescent / Female / Humans Language: En Journal: Tumori Year: 2018 Document type: Article Affiliation country: Italy