Document Detail


Splenogonadal fusion-a rare congenital anomaly demonstrated by 99Tc-sulfur colloid imaging: case report.
MedLine Citation:
PMID:  240914     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
A case report illustrating the value of spleen scanning in the diagnosis of a rare anomaly characterized by fusion of the spleen and left testis is described. This malformation results from faulty organogenesis during the fifth to the eighth week of fetal development. Only 65 cases have been reported in the world literature. In most instances, the anomaly is recognized as an incidental finding at autopsy or at surgical exploration of the abdomen. In 20% of cases the anomaly is associated with osseous malformations such as peromelia, ectromelia, micrognathia, and talipes.
Authors:
U Guarin; Z Dimitrieva; S J Ashley
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Journal of nuclear medicine : official publication, Society of Nuclear Medicine     Volume:  16     ISSN:  0161-5505     ISO Abbreviation:  J. Nucl. Med.     Publication Date:  1975 Oct 
Date Detail:
Created Date:  1975-12-18     Completed Date:  1975-12-18     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  0217410     Medline TA:  J Nucl Med     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  922-4     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
Clubfoot
Cryptorchidism
Humans
Infant
Male
Micrognathism
Radionuclide Imaging*
Spleen / abnormalities*
Technetium / diagnostic use*
Testis / abnormalities*
Chemical
Reg. No./Substance:
7440-26-8/Technetium

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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