Splenogonadal fusion - A review of rare anomaly.

dc.contributor.authorSuthar, Kaushal D
dc.contributor.authorMewada, Bhavna N
dc.date.accessioned2014-07-19T05:33:56Z
dc.date.available2014-07-19T05:33:56Z
dc.date.issued2013-01
dc.description.abstractSplenogonadal fusion is a rare congenital malformation that involves an abnormal connection between the spleen and the gonad or mesonephric derivatives. It manifests itself as a mass consisting of splenic and testicular or ovarian tissue. Splenogonadal fusion has been classified into two types; continuous, where there is a direct connection between spleen and gonad; and discontinuous, where ectopic splenic tissue is attached to the gonad, but there is no connection to the spleen. Many cases had an associated other anomalies either genital or systemic. Knowledge about the existence of such an uncommon entity is essential even to be suspected preoperatively as the appearance at exploration can be misleading as a malignant mass and often results in unnecessary gonadal removal.en_US
dc.identifier.citationSuthar Kaushal D , Mewada Bhavna N. Splenogonadal fusion - A review of rare anomaly. International Journal of Medical Science and Public Health. 2013 ; 2(1): 16-19.en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/152803
dc.language.isoenen_US
dc.source.urihttps://www.ijmsph.com/?mno=26711en_US
dc.subjectSplenogonadal Fusionen_US
dc.subjectCongenitalen_US
dc.subjectAnomalyen_US
dc.titleSplenogonadal fusion - A review of rare anomaly.en_US
dc.typeArticleen_US
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