ArticleInternational journal of women's health2025
Abdominopelvic Splenosis Resembling an Ovarian Malignancy: A Case Report.
Article in International journal of women's health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
2 citing papers in PubMed.
- Splenoses and Other Ectopic and Heterotopic Splenic Tissue: The Use of Long-Lasting Enhancement in Contrast-Enhanced Ultrasound to Avoid Unnecessary Intervention.Diagnostics (Basel, Switzerland) · 2026Review
- Omental Splenosis Mimicking Peritoneal Carcinomatosis.Mediterranean journal of hematology and infectious diseases · 2026Article
Corrections and comments
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: Splenosis is a benign condition that most commonly occurs following traumatic splenic rupture or splenectomy. It is characterized by ectopic autotransplantation of splenic tissue, typically within the abdominal or pelvic cavities. Due to its nonspecific clinical and imaging features, splenosis is often mistaken for malignant or metastatic disease, making accurate diagnosis a persistent clinical challenge. Materials and Methods: The diagnosis was established using multimodal imaging techniques, including transvaginal and abdominal ultrasonography with color Doppler flow imaging (CDFI), contrast-enhanced computed tomography (CECT) of the abdomen, and evaluation of serum tumor markers. Case Report: We report a case of a 31-year-old woman who underwent follow-up after an abortion and intrauterine device (IUD) placement. Transvaginal ultrasound revealed a hypoechoic, vascularized mass in the right adnexal region, which was attached to but poorly demarcated from the right ovary and adjacent bowel. Abdominal ultrasound failed to identify a spleen with typical features. Subsequent contrast-enhanced abdominal computed tomography (CECT) demonstrated multiple well-defined nodules with homogeneous soft tissue density throughout the right adnexal region, abdomen, and pelvis. Detailed medical history revealed prior traumatic splenic rupture with surgical repair. Based on these findings, a diagnosis of splenosis was established. As the patient remained asymptomatic, conservative management was adopted. Conclusion: This case highlights the importance of considering splenosis in the differential diagnosis of adnexal or abdominopelvic masses, particularly in patients with a history of splenic trauma or surgery. Accurate diagnosis depends on comprehensive imaging evaluation and thorough medical history review, which are critical to preventing misdiagnosis as malignancy and avoiding unnecessary surgical intervention.
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