Polysplenia syndrome in adulthood: a case report.

Autor: Malki, Manal Cherkaoui, Outznit, Mustapha, Mechhor, Salma, Bouibaouen, Boutaina, Nkurunziza, Lambert, El Bacha, Hicham, Benzzoubeir, Nadia, Laamrani, Fatime Zahrae, Jroundi, Laila, Errabih, Ikram
Předmět:
Zdroj: Pan African Medical Journal; Jan-Apr2022, Vol. 41, p1-6, 6p
Abstrakt: Polysplenia syndrome mainly described in pediatrics; rarely and incidentally in adulthood. Most patients had their diagnosis done during childhood due to the frequent association to cardiac anomalies that speak for themselves earlier in life. Multiple spleens, cardiac defect and vascular malformation of the inferior vena cava with azygos or hemiazygos continuation are the most frequent observed malformations. Our patient was one this rarest adulthood incidental diagnosis, who presented in the emergency department for nephritic colic, and while imaging for this, multiples spleens and other visceral malformations were diagnosed. Hopefully, cardiac ultrasound hadn't showed any cardiac malformation and the patient was discharged aware of this condition. Through this publication we report the possible incidental diagnosis of polysplenia condition and highlight the fact that people with such important malformation can lead a normal life, and only awareness should be given for future surgeries, instrumental treatment or else. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index