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Extensive noninvasive evaluations failed to demonstrate the disease in other extramedullary sites. The malignant cells were large and polymorphous; lacked terminal transferase; expressed surface CD\u20102, CD\u20103.<\/jats:p><jats:p>CD\u20108, and HLA\u2010DR antigens, and showed rearrangements of the T\u2010cell\u2010receptor \u03b2\u2010chain gene. To our knowledge, this type of lymphoma in an infant has not been reported before. Furthermore, aspergillosis is a rare presenting feature in patients with lymphoproliferative disease. In our case, it may reflect an underlying immune deficiency associated with the transformation and proliferation of a suppressor T cell.<\/jats:p>","DOI":"10.1002\/mpo.2950160314","type":"journal-article","created":{"date-parts":[[2007,2,20]],"date-time":"2007-02-20T17:54:03Z","timestamp":1171994043000},"page":"220-223","source":"Crossref","is-referenced-by-count":5,"title":["Immunoblastic peripheral T\u2010cell lymphoma confined to bone marrow in an infant presenting with aspergillosis"],"prefix":"10.1002","volume":"16","author":[{"given":"Rachelle","family":"Nuss","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Raul 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