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https://doi.org/10.21860/medflum2022_271165

Retroperitoneal localization of Castelman's disease in a pediatric patient: case report

Ema Šlabek orcid id orcid.org/0000-0001-8463-282X ; Sveučilište u Rijeci, Medicinski fakultet, Katedra za pedijatriju, Rijeka, Hrvatska
Harry Nikolić ; Sveučilište u Rijeci, Medicinski fakultet, Katedra za pedijatriju, Rijeka, Hrvatska; Klinički bolnički centar Rijeka, Klinika za dječju kirurgiju, Rijeka, Hrvatska
Ana Bosak Veršić ; Sveučilište u Rijeci, Medicinski fakultet, Katedra za pedijatriju, Rijeka, Hrvatska; Klinički bolnički centar Rijeka, Klinika za dječju kirurgiju, Rijeka, Hrvatska


Puni tekst: hrvatski pdf 2.874 Kb

str. 87-92

preuzimanja: 754

citiraj


Sažetak

Aim: Castelman's disease is a rare condition characterized by benign lymph node hyperplasia. The aim of this paper is to present Castelman's disease as a possible cause of retroperitoneal mass in the pediatric population. Case report: A fifteen-year-old boy was admitted to the Department of Pediatric Hematooncology for verification of an expansive formation in the area of omental bursa. The formation was detected by ultrasound during diagnostics due to recurrent vomiting. The boy complained of vomiting during ten days before admission, three to four times daily, usually after breakfast. Ultrasound showed a well-limited formation 4 x 3 centimeters in diameter located between the duodenum and pancreas. Computed tomography confirmed localisation of the tumor showing no signs of infiltration of surrounding structures and magnetic resonance imaging reported benign characteristics. Endoscopic ultrasound guided needle biopsy was preformed and a clinical presumption of a hyaline-vascular variant Castelman's disease was made. Surgical extirpation was performed. Complete tumor resection is a standard treatment for unicentric Castelman's disease. The pathological analysis confirmed the diagnosis of unicentric mixed variant Castelman's. Postoperative recovery went smoothly and the boy was discharged home in good general condition.There were no signs of recurrence of the underlying disease at regular check-ups. Conclusion: Although Castelman's disease is rare, especially localized retroperitoneally and in pediatric population, it should be included in the differential diagnosis when considering retroperitoneal tumorous formations.

Ključne riječi

Castleman disease; pediatrics; retroperitoneal neoplasms; vomiting

Hrčak ID:

271165

URI

https://hrcak.srce.hr/271165

Datum izdavanja:

1.3.2022.

Podaci na drugim jezicima: hrvatski

Posjeta: 2.265 *