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.
| Titel in Übersetzung | Splenogonadal fusion: Incidental finding in post-mortem imaging in a 63-year-old man |
|---|---|
| Originalsprache | Deutsch |
| Zeitschrift | Rechtsmedizin |
| Jahrgang | 27 |
| Ausgabenummer | 1 |
| Seiten (von - bis) | 27-32 |
| Seitenumfang | 6 |
| ISSN | 0937-9819 |
| DOIs | |
| Publikationsstatus | Veröffentlicht - 01.02.2017 |
UN SDGs
Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung
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SDG 3 – Gesundheit und Wohlergehen
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