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Similar Publications

Spinal ganglioneuroma: a rare and challenging tumor in the pediatric population.

Childs Nerv Syst

December 2024

Pediatric Neurosurgery Department, CHU de Brabois, Nancy, France.

Article Synopsis
  • Spinal ganglioneuromas are rare neuroblastic tumors mostly found in children, originating from sympathetic ganglia near the spine, and can lead to radicular or medullary symptoms when they extend into the spinal canal.
  • A thorough review of pediatric cases was conducted, highlighting a unique case treated in France, focusing on the thoraco-lumbar region due to its different surgical management requirements.
  • The review identified 21 pediatric patients, predominantly females, with the majority (42.85%) of tumors located in the thoracic spine, while the featured case presented unusual symptoms including abdominal pain and renal complications.
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Unusual case of a gigantic bladder mimicking a large pelvic cystic mass.

BJR Case Rep

March 2023

Department of Radiology, Northern Care Alliance, Bury, Lancashire, United Kingdom.

Pelvic masses are more common in females compared to the males. Bladder distension secondary to urinary retention can also mimic as a pelvic mass. However, it is rare to see chronic urinary retention with no clinical urinary symptoms.

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[Urological anomaly in an infant with Soto's syndrome: report of a case].

J Pediatr (Rio J)

January 1999

Fundação Universidade Federal do Rio Grande (FURG), Rio Grande, RS, Brazil.

OBJECTIVE: To discuss the diagnosis and the etiology of a bilateral urologic anomaly in a patient with Soto's Syndrome (cerebral gigantism). To alert the pediatric physicians and urologists about the coexistence of these two malformations. RESULTS: A three month old boy, born of a 35 week uncomplicated first pregnancy by cesarian, with phenotypic, radiologic and metacarpophalangeal profile of Soto's Syndrome was admitted to the Hospital because of hyperpnea, tachycardia and 39o C recurrent fever.

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Soto's syndrome, also known, as cerebral gigantism is a rare syndrome characterized by large size, large head and early psychomotor delay. Major diagnostic criteria include facial dysmorphisms, advanced bone age and developmental delay. Herein, a case of Soto's syndrome with rare finding of bilateral hydronephrosis and hydroureters is being reported.

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A 64-year-old man having backbone pain was referred to our institute, and laboratory examinations revealed that he was suffering from severe renal failure. Abdomino-pelvic CT revealed bilateral hydronephrosis, a giant prostate over 500 g in weight, and multiple para-aortic lymph node metastasis. Histological diagnosis of the prostate was small cell neuroendocrine carcinoma.

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