ganglioneuroma/lafyèv

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5 rezilta yo

Intermittent Fever, Progressive Weight Gain, and Personality Changes in a Five-Year-Old Girl: Unusual Paraneoplastic Syndrome due to Presacral Ganglioneuroma.

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Ganglioneuromas are rare tumors in the neuroblastoma group. Paraneoplastic syndrome (PNS) due to presacral ganglioneuromas was hardly reported in previous literature. Here, we reported that a case of a 5-year-old girl with a presacral ganglioneuroma presented with PNS, who presented with

Resection of a thoracoabdominal ganglioneuroma via a retroperitoneal minimally invasive approach.

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A 10-year-old girl presented to her pediatrician with a history of cough and fever. A chest radiograph revealed a paraspinal mass. On cross-sectional imaging, the mass traversed the diaphragm, extending from T9 to L1 spinal levels with involvement of the T10-12 neural foramen. Vanillylmandelic and

Neuroblastoma with concomitant giardiasis: report of a case with diagnosis by fine needle aspiration cytology.

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BACKGROUND Diagnosis of two pathologies, including a neoplasm and infectious condition, by fine needle aspiration (FNA) cytology in the same patient is rare. METHODS A 2-year-old, male child presented with fever, abdominal pain and abdominal mass. Imaging findings were strongly in favor of a

Neuroblastoma in children: a 10-year experience in Saudi Arabia.

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Twenty children with biopsy-proven neuroblastoma were diagnosed and treated between 1984 and 1994 at King Fahd Hospital of the University in Al-Khobar, Saudi Arabia. There were 12 males and eight females with a ratio of 1.5/1. The median age at diagnosis was 3 years. Clinical staging showed: Stage

Clinical characteristics of adrenal tumors in children: a retrospective review of a 15-year single-center experience.

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OBJECTIVE Adrenal tumors are rare in children. The aim of this study is to review and analyze clinical data on the diagnosis and management of adrenal tumors in children. METHODS Between 2001 and 2015, 48 pediatric patients (<14 years old) admitted to our institute with adrenal tumors were reviewed.

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