Evidence map›Paper›PMID 41847315›Full record

ArticleInternational medical case reports journal2026

Double Torsion of a Continuous Type of a Splenogonadal Fusion Presenting as an Inguinoscrotal Emergency: A Rare Case Report.

Osama Ahmad, Abdulrahman Shbani, Yahia Ranjous, Osaid Alkhabbaz, Abd Almueen Mohammad Khabbaz

Abstract readCase Reports
In one paragraph

Article in International medical case reports journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Osama AhmadFaculty of Medicine, Damascus University, Damascus, Syria.
Abdulrahman ShbaniFaculty of Medicine, Tartous University, Tartous, Syria.
Yahia RanjousFaculty of Medicine, Damascus University, Damascus, Syria.ORCID 0009-0005-1681-2198
Osaid AlkhabbazFaculty of Medicine, Damascus University, Damascus, Syria.
Abd Almueen Mohammad KhabbazGeneral Surgery Department, Hama National Hospital, Hama, Syria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Splenogonadal fusion (SGF) is a rare congenital anomaly that presents with an abnormal connection between the gonad and the spleen. Misdiagnosis can lead to unnecessary surgical interventions, underscoring the need for thorough pre-operative assessments and differential diagnoses. Histopathological and imaging evaluations are essential for accurate diagnosis and appropriate management. Case Presentation: A 35-year-old male presented with an acute swelling and pain in the scrotum and the inguinal region. The patient's medical and surgical history was unremarkable, with no known congenital anomalies. Emergency surgery revealed a fibrous cord extending between the orthotopic spleen and the left testis with multiple tissue formations along it in a rosary-like shape. The reason for the acute presentation was double torsion of the abnormal cord at the internal inguinal ring and near the junction between the fibrous cord and the testis. The abnormal tissue was resected and histopathological examination confirmed splenic tissue. confirming the final diagnosis of splenogonadal fusion (continuous form). Conclusion: SGF is a rare congenital anomaly which is difficult to diagnose that is difficult to diagnose due to its nonspecific clinical presentation. Most SGF cases are diagnosed during the exploratory surgery, no single definitive diagnostic modality exists; however, imaging and splenic scintigraphy may aid in selected cases. Surgeons should consider this benign condition in the differential diagnoses of left inguinal or scrotal masses to avoid unnecessary orchiectomy.

Indexed as

congenital anomalyinguinal masssplenogonadal fusiontesticular torsion

Identifiers

PMID41847315
PMCPMC12991299

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