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A rarely encountered but distinctive type of aggressive malignant tumor of childhood and adolescence has been recently described as occurring predominantly or exclusively intrabdominally. It is characterized by a generally diffuse pattern of growth of small cells with hyperchromatic nuclei, scanty cytoplasm, patchy epithelial differentiation, immunohistochemical co-expression of keratin and desmin intermediate filaments and a focal but pronounced desmoplastic stromal component. It is regarded as yet another variant in the group of small round cell tumors (SRCT) of infancy and childhood. This case report of a mass in the greater omentum of a 15 yr-old girl adds to the 33 cases already described in the English literature.
G Yeoh, and
P Russell, and
E J Wills, and
S Fleming
January 1999,
The Yale journal of biology and medicine,
G Yeoh, and
P Russell, and
E J Wills, and
S Fleming
January 2014,
Annals of gastroenterology,
G Yeoh, and
P Russell, and
E J Wills, and
S Fleming
January 2001,
The Yale journal of biology and medicine,
G Yeoh, and
P Russell, and
E J Wills, and
S Fleming
December 2006,
JPMA. The Journal of the Pakistan Medical Association,
G Yeoh, and
P Russell, and
E J Wills, and
S Fleming
January 2000,
Journal of gastroenterology,
G Yeoh, and
P Russell, and
E J Wills, and
S Fleming
December 2014,
Journal of gastrointestinal cancer,
G Yeoh, and
P Russell, and
E J Wills, and
S Fleming
February 2015,
The Indian journal of surgery,
G Yeoh, and
P Russell, and
E J Wills, and
S Fleming
January 2004,
Revue medicale de Liege,
G Yeoh, and
P Russell, and
E J Wills, and
S Fleming
December 2000,
Archives of pathology & laboratory medicine,
G Yeoh, and
P Russell, and
E J Wills, and
S Fleming
January 2015,
Cirugia y cirujanos,
