Unusual Presentation of Splenogonadal Fusion in a 7-Month-Old Male Infant

被引:0
作者
Ghorbani, Hamidreza [1 ]
Alimohammadi, Sina [2 ]
Jamshidi, Shirin Taraz [3 ]
Mirsani, Amin [1 ]
机构
[1] Mashhad Univ Med Sci, Kidney Transplantat Complicat Res Ctr, Mashhad, Razavi Khorasan, Iran
[2] Mashhad Univ Med Sci, Student Res Comm, Mashhad, Razavi Khorasan, Iran
[3] Mashhad Univ Med Sci, Imam Reza Hosp, Dept Pathol, Mashhad, Razavi Khorasan, Iran
来源
INTERNATIONAL JOURNAL OF PEDIATRICS-MASHHAD | 2020年 / 8卷 / 02期
关键词
Infant; Iran; Splenogonadal fusion; Testicular neoplasm; Orchiectomy;
D O I
10.22038/ijp.2019.41498.3499
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Introduction: Splenogonadal fusion is a rare congenital anomaly characterized with anomalous fusion of the spleen and the gonad or mesonephric derivatives. Herein, we report the case of a 7-month-old boy with unusual presentation of splenogonadal fusion. Case Presentation: A 7-month-old boy was brought to the Urology Clinic, Imam Reza Hospital, Mashhad, Iran, by his parents complaining of a painless palpable scrotal mass with a sudden increase in the size after a respiratory infection. The patient underwent surgery with a suspicion of testicular malignant tumors. However, pathologic study revealed a benign mass with splenic origin. Conclusion: Preoperative diagnosis of splenogonadal fusion is almost impossible and most cases undergo an unnecessary orchiectomy, especially when the clinical presentation resembles a primary testicular neoplasm. Although surgery is necessary to remove the benign splenic tissue as well, proper knowledge and consideration along with appropriate imaging studies and histopathological examination contribute in avoiding an unnecessary orchiectomy.
引用
收藏
页码:10905 / 10910
页数:6
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