Abstract
Splenogonadal fusion (SGF) is a rare malformation occurring in both men and women (male-female ratio 16.6:1). This generally relatively rare benign embryonic malformation has been described in the literature often in the form of a case report, mainly by urologists, pediatric surgeons, radiologists and pathologists. A case of a 63-year-old man with no external deformities in whom SGF of the continuous type was documented as an incidental finding during a forensic autopsy and in the post-mortem computed tomography (CT) is described. A comparison with the international literature shows that this case constitutes a great rarity within the last 20 years.
Dokumententyp: | Zeitschriftenartikel |
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Fakultät: | Medizin |
Themengebiete: | 600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin und Gesundheit |
ISSN: | 0937-9819 |
Sprache: | Englisch |
Dokumenten ID: | 55223 |
Datum der Veröffentlichung auf Open Access LMU: | 14. Jun. 2018, 09:58 |
Letzte Änderungen: | 04. Nov. 2020, 13:35 |