2010
DOI: 10.1016/j.jpedsurg.2010.04.020
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Sclerosing angiomatoid nodular transformation of the spleen in an adolescent with chronic abdominal pain

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Cited by 21 publications
(9 citation statements)
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“…Our case described a rare finding of SANT in the paediatric population with histological characteristics of slit-like or irregular shaped vascular spaces that was typical of SANT. Immunohistochemistry was positive for CD8-, CD31+ and CD34+, which was in keeping with results found in previous cases [2,9]. In addition, we also found CD240 to be positive.…”
Section: Discussionsupporting
confidence: 92%
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“…Our case described a rare finding of SANT in the paediatric population with histological characteristics of slit-like or irregular shaped vascular spaces that was typical of SANT. Immunohistochemistry was positive for CD8-, CD31+ and CD34+, which was in keeping with results found in previous cases [2,9]. In addition, we also found CD240 to be positive.…”
Section: Discussionsupporting
confidence: 92%
“…SANT in children is exceptionally rare and review of the existing literature in children less than 18 years old revealed 4 patients, with a median age of 10.5 years (range: 3-17 years), of which 75% (n=3) males [2,3,10,11]. (Table1).…”
Section: Discussionmentioning
confidence: 99%
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“…Nevertheless, the high frequency of complications such as bleeding or splenic rupture was noted after percutaneous biopsy of vascular splenic regions. To the best of our knowledge, there were six cases reported in English literatures that were diagnosed as a SANT by imaging study and follow-up, and operations were finally completed, according to the growing mass ( Table 1 ) [14] , [15] , [16] , [17] , [18] , [19] . The follow-up period ranged from 3 to 36 months.…”
Section: Discussionmentioning
confidence: 99%