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.
Zusammenfassung
Die splenogonadale Fusion (SGF) ist eine seltene Fehlbildung, die bei Männern und Frauen zu finden ist (Verhältnis von Männern zu Frauen: 16,6:1). Diese i. Allg. gutartige embryonale Fehlbildung wurde in der Literatur – meist in Form von „case reports“ – v. a. von Urologen, Kinderchirurgen, Radiologen oder Pathologen beschrieben. Im gegenständlichen Fall eines 63 Jahre alt gewordenen Mannes wurde die SGF vom kontinuierlichen Typ erst als postmortaler Zufallsbefund im Rahmen der gerichtlichen Sektion und postmortalen bildgebenden Untersuchung festgestellt. Eine ausführliche internationale Literaturrecherche konnte zeigen, dass es sich bei dieser Konstellation um einen in den letzten 20 Jahren sehr seltenen Befund handelt.
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N. Wilke-Schalhorst, C. Braun, H. Vogel and K. Püschel state that they have no competing interests.
This article does not contain any studies with human participants or animals performed by any of the authors. All investigations described in the present manuscript were carried with the approval of the responsible ethics committee and in accordance with national law and the Helsinki Declaration from 1975 (in its current revised form). Informed consent was obtained from the relatives or legal guardian of the subject identifiable from images or other information within the manuscript.
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Wilke-Schalhorst, N., Braun, C., Vogel, H. et al. Splenogonadal fusion. Rechtsmedizin 27, 27–32 (2017). https://doi.org/10.1007/s00194-016-0125-y
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DOI: https://doi.org/10.1007/s00194-016-0125-y
Keywords
- Testicular mass
- Post-mortem computed tomography
- Congenital abnormalities
- Malformation
- Splenogonadal fusion