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一例原发性结外非霍奇金淋巴瘤首次表现为腕部周围软组织肿胀的病例报告。

A Case Report of Primary Extranodal Non-hodgkin Lymphoma First Presentation as a Soft Tissue Swelling Around the Wrist.

作者信息

Sopu Alexandra, Green Connor, McHugh Gavin, Quinlan John

机构信息

Department of Trauma and Orthopaedics, Royal College of Surgeons, Ireland.

出版信息

J Orthop Case Rep. 2015 Apr-Jun;5(2):3-5. doi: 10.13107/jocr.2250-0685.284.

Abstract

INTRODUCTION

Primary musculoskeletal extranodal non-Hodgkin lymphoma is a rare presentation and account for 5% of all primary extranodal non-Hodgkin lymphomas. Treatment uses a combination of chemotherapy and radiotherapy with good prognosis in unifocal manifestation. We report an unusual case of primary musculoskeletal extranodal lymphoma presenting as a soft tissue swelling around the wrist.

CASE REPORT

A 75 year old lady was referred to the Orthopaedic Outpatients Department with a painless, slowly growing mass on the dorsum of the right wrist. Clinical examination revealed a 6 X 9 cm round painless mass on the dorsum of the distal radius adherent to both the underlying structures and skin. MRI of the wrist showed a large mass causing extensive osteolysis of the distal radius and extending proximally with abnormal replacement of the marrow. The patient was brought to theatre for biopsy and subsequent histopathological examination confirmed a B-cell non-Hodgkin lymphoma. The patient was referred to the Haematology Service for further treatment and follow-up. She received chemotherapy and radiotherapy with satisfactory results.

CONCLUSION

Lymphoma presenting as a soft tissue mass is relatively uncommon and can easily be confused with a wide variety of inflammatory conditions, more common neoplasias as well as infectious diseases (tuberculosis). Though rare, extranodal lymphoma should be regularly included in the differential diagnosis of mass lesions.

摘要

引言

原发性肌肉骨骼结外非霍奇金淋巴瘤是一种罕见的表现形式,占所有原发性结外非霍奇金淋巴瘤的5%。对于单灶性表现的患者,治疗采用化疗和放疗相结合的方法,预后良好。我们报告一例罕见的原发性肌肉骨骼结外淋巴瘤,表现为腕部周围软组织肿胀。

病例报告

一名75岁女性因右腕背部无痛性、生长缓慢的肿块被转诊至骨科门诊。临床检查发现桡骨远端背部有一个6×9厘米的圆形无痛性肿块,与下方结构和皮肤均粘连。腕部MRI显示一个大肿块,导致桡骨远端广泛骨质溶解,并向近端延伸,骨髓被异常取代。患者被送往手术室进行活检,随后的组织病理学检查证实为B细胞非霍奇金淋巴瘤。患者被转诊至血液科接受进一步治疗和随访。她接受了化疗和放疗,效果满意。

结论

表现为软组织肿块的淋巴瘤相对少见,容易与多种炎症性疾病、更常见的肿瘤以及传染病(如结核病)相混淆。尽管罕见,但在肿块病变的鉴别诊断中应常规考虑结外淋巴瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51c9/4722583/2a97e58afc68/JOCR-5-3-g001.jpg

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