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Musculoskeletal lymphoma: MRI of bone or soft tissue presentations

医学 软组织 磁共振成像 淋巴瘤 病理 放射科 软组织病理学 病变 皮下组织
作者
G.M.A. Carroll,William Breidahl,Peter Robbins
出处
期刊:Journal of Medical Imaging and Radiation Oncology 卷期号:57 (6): 663-673 被引量:21
标识
DOI:10.1111/1754-9485.12071
摘要

Abstract Aim To assess the MRI findings of musculoskeletal lymphoma primarily presenting clinically as a bone lesion or soft tissue mass. Methods Magnetic resonance imaging of 23 cases of musculoskeletal lymphoma were retrospectively reviewed. Features assessed included tumour location, morphology, signal intensity ( SI ) characteristics, cortical destruction, involvement of multiple anatomic compartments, encasement of adjacent neurovascular structures/tendons and subcutaneous oedema. Results Osseous lesions were typically poorly defined and hypointense on T 1‐weighted imaging. T 2‐weighted SI was usually heterogeneous, with 54% of cases having a ‘mosaic’ pattern of marrow replacement. Ninety‐two per cent of osseous tumours had cortical abnormalities, most commonly a permeative pattern. A periosseous soft tissue cuff was present in 46% of cases while 38% had a more significant extraosseous component. All cases of soft tissue lymphoma were iso‐/slightly hyperintense to muscle on T 1‐weighted images and hyperintense on T 2‐weighted images. Multicompartment involvement by extraosseous tumour was present in 75% of cases, and 67% had subcutaneous oedema. Eighty‐three per cent of soft tissue tumours showed encasement of adjacent structures. Multifocal lymphoma had similar morphology and SI characteristics to single‐site lesions. Histopathologically, there were 21 cases of non‐ H odgkin's lymphoma and two of H odgkin's lymphoma. Conclusion Magnetic resonance imaging features of primary osseous lymphoma include T 2 heterogeneity, a periosseous soft tissue cuff or a more substantial mass, and cortical disruption often disproportionate to the extent of extraosseous tumour. Features characteristic of soft tissue lymphoma include relative homogeneity on T 1‐ and T 2‐weighted imaging, multicompartment involvement and encasement of neurovascular structures.
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