scholarly journals Splenogonadal fusion: a radiologic-pathologic correlation and review of the literature

2020 ◽  
Vol 15 (10) ◽  
pp. 1817-1822
Author(s):  
Amir Qadeer ◽  
Caroline Quincey ◽  
Kanwar Gill ◽  
Michael Paddock
2009 ◽  
Vol 76 (2) ◽  
pp. 137-139 ◽  
Author(s):  
M. Arancio ◽  
C. Marchetti ◽  
G. Landi ◽  
A. Mina ◽  
A. Delsignore ◽  
...  

Splenogonadal fusion (SGF) is a rare congenital abnormality in which there is a fusion between spleen and gonad. Approximately 150 cases have been described in world literature. SGF can be continuous, where there is a connection between ectopic and orthotopic spleen, and discontinuous, with no connection. In our paper we report a case of SGF in a 36-year-old female with ultrasound and MR findings of space-occupying lesion in lower abdomen, and a review of the literature.


2006 ◽  
Vol 88 (2) ◽  
pp. 163-164 ◽  
Author(s):  
KP Kennedy ◽  
S Barnard ◽  
MJ Speakman

Splenogonadal fusion is a rare congenital abnormality. In this case report, the diagnosis of splenogonadal fusion was made after the removal of an abnormal mass at ‘routine’ left herniotomy. A cautious approach at surgery resulted in no apparent damage to the testicle. A short review of the literature is included.


1996 ◽  
Vol 155 (1) ◽  
pp. 309-311 ◽  
Author(s):  
Mulhammet Ihsan Karaman ◽  
Edmond T. Gonzales

2013 ◽  
Vol 6 (3) ◽  
pp. 816-818 ◽  
Author(s):  
WAN-FU LI ◽  
MEI-XIANG LUAN ◽  
ZHU MA ◽  
YA-JUN CHEN

2014 ◽  
Vol 2 (2) ◽  
pp. 67-69 ◽  
Author(s):  
Cinzia Chiaramonte ◽  
Fortunato Siracusa ◽  
Giuseppe Li Voti

2016 ◽  
Vol 24 ◽  
pp. 30-34 ◽  
Author(s):  
Elizabeth J. Cochran ◽  
Abraham Schlauderaff ◽  
Scott D. Rand ◽  
Gerald W. Eckardt ◽  
Shekar Kurpad

2012 ◽  
Vol 10 (1) ◽  
pp. 92-95 ◽  
Author(s):  
Roberto Iglesias Lopes ◽  
Mabel Tatty de Medeiros ◽  
Marco Antônio Arap ◽  
Marcello Cocuzza ◽  
Miguel Srougi ◽  
...  

A 36 year-old man after tests for assessing male infertility was diagnosed with primary infertility, bilateral cryptorchidism, non-obstructive azoospermia and discontinuous splenogonadal fusion. Carcinoma in situ was found in his left testicle, which was intra-abdominal and associated with splenogonadal fusion. To our knowledge, this is the fourth case of splenogonadal fusion associated with testicular cancer reported. One should always bear in mind the possibility of this association for the left cryptorchid testicle.


2020 ◽  
Vol 2020 ◽  
pp. 1-7
Author(s):  
Youssef Kadouri ◽  
Damien Carnicelli ◽  
Hachem El Sayegh ◽  
Lounis Benslimane ◽  
Yassine Nouini

Introduction. Splenogonadal fusion is a rare congenital anomaly, defined by the presence of ectopic splenic tissue caused by an abnormal connection between the spleen and the gonad or mesonephrotic derivatives during the embryonic period. Materials and Methods. By reporting an observational case and performing a review of the literature according to the CARE guidelines (using the PubMed database and guidelines from urology, general surgery, and pediatric learned societies), we present the embryological genesis of the splenogonadal fusion, the associated anatomical anomalies, and the diagnostic procedure. Observation. We report the case of a patient aged 45, with no notable history, reporting left testicular pain. A small nodule on the upper pole of the left testicular was clinically palpable. Tumor markers were normal, and scrotal ultrasound depicted a hypoechoic hypervascular nodule measuring 8∗6∗8 mm. After validation in a multidisciplinary oncology consultation meeting and opinion from a uro-andrologist expert, the patient underwent an inguinal lumpectomy with an extemporaneous examination which did not objectify any signs of malignancy. Ultimately, it is a normal spleen tissue in the testicular ectopic position. Discussion. Splenogonadal fusion corresponds to a rare congenital malformation; less than 200 cases have been published in the literature, most often affecting boys, with a sex ratio of 15/1. Two types are described, depending on the continuity of the link between the orthotopic spleen and the gonad: the continuous and discontinuous forms. In a third of the cases, there are associated congenital malformations and particularly in the continuous forms (44 to 50% of the cases): anomalies of the limbs, micrognathia, microgyria, and hepatic and digestive abnormalities. Cryptorchidism is associated with the continuous form in 31% of cases. The preoperative diagnosis remains difficult because of its morphological and clinical characteristics suggesting a tumor process.


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