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Polysplenia syndrome in adulthood: a case report

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 malformatio...

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Detalles Bibliográficos
Autores principales: Malki, Manal Cherkaoui, Outznit, Mustapha, Mechhor, Salma, Bouibaouen, Boutaina, Nkurunziza, Lambert, Bacha, Hicham El, Benzzoubeir, Nadia, Laamrani, Fatime Zahrae, Jroundi, Laila, Errabih, Ikram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8933446/
https://www.ncbi.nlm.nih.gov/pubmed/35371381
http://dx.doi.org/10.11604/pamj.2022.41.67.29014
Descripción
Sumario: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.