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http://dx.doi.org/10.1177/1066896918810428 | DOI Listing |
Int J Surg Pathol
August 2019
1 Hartford Hospital, Hartford, CT, USA.
Schmerz
August 2008
Klinik für Allgemeine Chirurgie, Viszeral-, Gefäss- und Kinderchirurgie, Universitätsklinikum des Saarlandes, Kirrberger Strasse, 66424, Homburg/Saar, Deutschland.
A 39-year-old female patient presented with a 3-year history of lower back pain which had not been alleviated by pain treatment combined with physiotherapy. Radiological findings were normal with the exception of a cystic paravertebral tumor in the left retroperitoneum. The cyst was primarily regarded as a coincidental finding because no criteria for malignancy were present.
View Article and Find Full Text PDFPediatr Blood Cancer
August 2004
Department of Pediatric Oncology, Ankara University Faculty of medicine, Cebeci Ankara, Turkey.
The current report describes a 23-month-old boy with paratesticular rhabdomyosarcoma who was incidentally diagnosed as also having an isolated mediastinal cystic lymphangioma. The association of childhood rhabdomyosarcoma with various congenital anomalies and genetic alterations such as p53 mutations have been well known. However, mediastinal cystic lymphangioma has not been reported among the congenital anomalies diagnosed in rhabdomyosarcoma.
View Article and Find Full Text PDFJ Pediatr Surg
August 2003
Department of Pediatric Surgery, Celal Bayar University, Medical School, Manisa, Turkey.
Cystic lymphangiomas, which are localized on the mesentery of the intestine, are rarely seen. The presence of intestinal atresia together with cystic lymphangioma in the same location has never been described before. In this study, a premature girl weighing 2,630 g who had jejunal atresia, cystic lymphangioma localized in the mesentery of the distal atretic jejunal segment, and multiple rib anomalies is presented.
View Article and Find Full Text PDFAm Surg
July 1989
Department of Pathology, Cleveland Metropolitan General Hospital, Case Western Reserve University, OH 41109.
An exceedingly rare tumor was found coincidentally in a young woman who had salpingectomy. The benign tumor was complex in nature and consisted of a lymphangioma and a well-encapsulated lipoma located in the mesentery of the small intestine. This tumor is compared with the similar ones mentioned so far in the literature.
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