Literature DB >> 18484478

Primary hepatic Burkitt lymphoma.

Elpis Mantadakis1, Maria Raissaki, Maria Tzardi, Nikolaos Katzilakis, Athanasios Chatzimichael, Maria Kalmanti.   

Abstract

Primary hepatic lymphomas are exceedingly rare in children, with less than a dozen cases described to date. The authors present an 8.5-year-old boy with Burkitt lymphoma of the liver who had isolated multifocal liver lesions that exhibited a multilayered progressive enhancing pattern on MRI. Diagnosis was achieved after laparotomy and incisional biopsy that failed to detect disease outside the liver. The patient received short, intensive multiagent chemotherapy. He is currently well 22 months after the end of chemotherapy. This case illustrates that clinical judgment in conjunction with unusual imaging findings may contribute to the diagnosis of common tumors in rare locations.

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Year:  2008        PMID: 18484478     DOI: 10.1080/08880010802016466

Source DB:  PubMed          Journal:  Pediatr Hematol Oncol        ISSN: 0888-0018            Impact factor:   1.969


  1 in total

Review 1.  Primary hepatic lymphoma: dilemmas in diagnostic approach and therapeutic management.

Authors:  Aikaterini Mastoraki; Maria Ioanna Stefanou; Evangelos Chatzoglou; Nikolaos Danias; Maria Kyriazi; Nikolaos Arkadopoulos; Vasilios Smyrniotis
Journal:  Indian J Hematol Blood Transfus       Date:  2013-05-15       Impact factor: 0.900

  1 in total

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