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一名13岁女性,患有原发性骨T细胞丰富型B细胞淋巴瘤,临床表现为慢性复发性多灶性骨髓炎。

A thirteen year old female with primary T-cell rich B-cell lymphoma of bone masquerading as chronic recurrent multifocal osteomyelitis.

作者信息

Haque Saadiya A, Shad Aziza, Ozdemirli Metin, Shanmugam Victoria K, Kallakury Bhaskar

机构信息

Department of Pathology;

出版信息

Pediatr Rep. 2009 Jun 8;1(1):e3. doi: 10.4081/pr.2009.e3.

Abstract

Primary lymphoma of the bone (PLB) accounts for 2% of all non-Hodgkin's lymphomas, and until recently it had not been well characterized in literature. Most cases present in adulthood (average age 50), with localized painful lesions in the long bones, cranium, or axial skeleton.We describe a case of multifocal PLB in an adolescent female. In this case, the initial presentation, with migratory large joint polyarthralgias and bone pain, mimicked chronic recurrent multifocal osteomyelitis (CRMO). Had a biopsy not been performed the diagnosis would have been missed.

摘要

原发性骨淋巴瘤(PLB)占所有非霍奇金淋巴瘤的2%,直到最近其在文献中仍未得到很好的描述。大多数病例发生在成年期(平均年龄50岁),表现为长骨、颅骨或中轴骨骼的局限性疼痛性病变。我们描述了一例青春期女性多灶性PLB病例。在该病例中,最初表现为游走性大关节多关节痛和骨痛,酷似慢性复发性多灶性骨髓炎(CRMO)。若未进行活检,可能会漏诊。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43e9/3096024/bfec570eb20a/pr-2009-1-e3-g001.jpg

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