Splenogonadal fusion in a female: A case report of a rare congenital anomaly.

Autor:	Mohamed SEMK; Body Imaging Department, HGH, Hamad Medical Corporation, Doha, Qatar., Elawad MF; Hamad Medical Corporation, Doha, Qatar., Mohamed MA; Body Imaging Department, HGH, Hamad Medical Corporation, Doha, Qatar., Hussain SA; Hamad Medical Corporation, Doha, Qatar., Al-Rashid AA; Department of Radiology-College of Medicine, Qatar University, Hamad Medical Corporation, Doha, Qatar.
Jazyk:	angličtina
Zdroj:	Radiology case reports [Radiol Case Rep] 2024 Jan 16; Vol. 19 (4), pp. 1409-1412. Date of Electronic Publication: 2024 Jan 16 (Print Publication: 2024).
DOI:	10.1016/j.radcr.2023.12.054
Abstrakt:	We present a case of an 18-year-old female referred for an MRI pelvis to evaluate suspected uterine anomaly by ultrasound. The MRI showed a complete septate uterus and in addition, an elongated tubular structure (isointense to the spleen) extending from the left ovary in the left retroperitoneal region/left paracolic gutter to the under-splenic surface. CT abdomen and pelvis revealed this to be a similarly enhancing structure as the spleen and appears as a tubular retroperitoneal structure connecting the left ovary to the spleen with associated vasculature joining the splenic vein cranially and the ovarian vessels caudally consistent with splenogonadal fusion. (© 2023 The Authors. Published by Elsevier Inc. on behalf of University of Washington.)
Databáze:	MEDLINE
Externí odkaz:	Zobrazit plný text záznamu