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A Rare Case of Continuous Type Splenogonadal Fusion in a Young Male with Primary Infertility
Author(s) -
Santosh Kumar,
Kumar Jayant,
Swati Agrawal,
Kalpesh Parmar,
Shrawan Kumar Singh
Publication year - 2014
Publication title -
case reports in urology
Language(s) - English
Resource type - Journals
eISSN - 2090-696X
pISSN - 2090-6978
DOI - 10.1155/2014/796761
Subject(s) - primary infertility , medicine , mesonephric duct , abdomen , infertility , pelvis , differential diagnosis , radiology , pregnancy , pathology , genetics , biology , kidney
Splenogonadal fusion is a rare developmental anomaly in which an abnormal connection between splenic tissue and gonads or mesonephric derivatives is present. Here we present a case of young man with the complaint of primary infertility for 3 years. On evaluation (USG and MRI abdomen and pelvis), his right scrotal testis was atrophied and left intra-abdominal undescended testis. On laparoscopic assessment, a mass was seen on the left side due to continuous type of splenogonadal fusion for which excision and left orchidectomy were done. Postoperative period was uneventful and he was discharged under satisfactory condition. Splenogonadal fusion is a rare entity and it is commonly mistaken for testicular tumour. It should be considered in the differential diagnosis of testicular masses especially when there are associated congenital anomalies and preoperative laparoscopic assessment, should be done to avoid unnecessary radical surgery.

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