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小指骨原发性淋巴瘤:一例报告并文献复习。

Primary lymphoma of bone of the little finger: a case report and review of the literature.

机构信息

Department of Radiology, Oregon Health & Science University, Portland, OR, USA.

Department of Pathology, Oregon Health & Science University, Portland, OR, USA.

出版信息

Skeletal Radiol. 2024 Aug;53(8):1645-1650. doi: 10.1007/s00256-024-04576-9. Epub 2024 Jan 16.

Abstract

Primary lymphoma of bone (PLB) is a rare, malignant lymphoid proliferation within bone accounting for less than 3% of all malignant bone tumors. In this case report, a 61-year-old female with past medical history of gout presented with pain and swelling in her right little finger. Initial radiographs demonstrated periostitis and soft tissue swelling about the right little finger. She returned three months later with progressive pain. Subsequent MRI and repeat radiographs demonstrated near complete destruction of the right little finger middle phalanx and periostitis with marrow infiltration at the right long finger. Given the rapid progression of disease, the differential diagnosis consisted primarily of aggressive neoplastic processes. The little finger ray was amputated through the level of the metacarpophalangeal joint and histopathology demonstrated large neoplastic cells that stained positive with CD45, CD20, and PAX5, compatible with diffuse large B-cell lymphoma. A subsequent normal bone marrow aspiration and PET-CT demonstrated no additional sites of disease, thus excluding secondary lymphoma to bone. To the best of our knowledge, this is the first case report of polyostotic PLB involving the hand. PLB of the hands may be initially misdiagnosed due to its rarity and clinical presentation mimicking rheumatological disease. Clinical vigilance in concert with close imaging follow-up is required to make the diagnosis in a timely fashion. We also review the existing PLB hand literature which consists of five cases.

摘要

原发性骨淋巴瘤(PLB)是一种罕见的恶性淋巴组织增生,占所有恶性骨肿瘤的比例不到 3%。在本病例报告中,一名 61 岁女性,既往有痛风病史,出现右手小指疼痛和肿胀。最初的 X 线片显示小指周围骨膜炎和软组织肿胀。三个月后她因疼痛加重而再次就诊。随后的 MRI 和重复 X 线片显示右手小指中节指骨几乎完全破坏,伴有骨膜炎和右手食指骨髓浸润。鉴于疾病的快速进展,主要鉴别诊断为侵袭性肿瘤性病变。小指通过掌指关节水平被截断,组织病理学显示大的肿瘤细胞 CD45、CD20 和 PAX5 阳性,符合弥漫性大 B 细胞淋巴瘤。随后的正常骨髓抽吸和 PET-CT 显示无其他部位的疾病,因此排除了继发性骨淋巴瘤。据我们所知,这是首例累及手部的多灶性 PLB 病例。由于其罕见性和临床表现类似于风湿病,手部的 PLB 可能最初被误诊。为了及时做出诊断,需要临床警惕并密切影像学随访。我们还回顾了现有的关于手部 PLB 的文献,其中包括 5 例病例。

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