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Extranodal NK/T-cell Lymphoma Mimicking Granulomatous Myositis.模仿肉芽肿性肌炎的结外NK/T细胞淋巴瘤
Intern Med. 2019 Jan 15;58(2):277-282. doi: 10.2169/internalmedicine.0859-18. Epub 2018 Aug 24.
2
Skeletal Muscle Lymphoma Presenting with Chronic Compartment Syndrome of Leg after Trauma.创伤后出现腿部慢性骨筋膜室综合征的骨骼肌淋巴瘤
Case Rep Oncol Med. 2018 Apr 1;2018:4078672. doi: 10.1155/2018/4078672. eCollection 2018.
3
CD30 expression and survival in extranodal NK/T-cell lymphoma: a systematic review and meta-analysis.结外NK/T细胞淋巴瘤中CD30表达与生存情况:一项系统评价和Meta分析
Oncotarget. 2018 Jan 8;9(23):16547-16556. doi: 10.18632/oncotarget.24044. eCollection 2018 Mar 27.
4
Primary skeletal muscle diffuse large B cell lymphoma: A case report and review of the literature.原发性骨骼肌弥漫性大B细胞淋巴瘤:一例报告并文献复习
Oncol Lett. 2015 Oct;10(4):2156-2160. doi: 10.3892/ol.2015.3505. Epub 2015 Jul 17.
5
CD56-negative extranodal NK/T cell lymphoma should be regarded as a distinct subtype with poor prognosis.CD56阴性的结外NK/T细胞淋巴瘤应被视为一种预后较差的独特亚型。
Tumour Biol. 2015 Sep;36(10):7717-23. doi: 10.1007/s13277-015-3485-0. Epub 2015 May 3.
6
NK/T cell lymphoma associated with peripheral eosinophilia.与外周嗜酸性粒细胞增多相关的NK/T细胞淋巴瘤
Malays J Pathol. 2014 Dec;36(3):201-5.
7
CD30 extranodal natural killer/T-cell lymphoma mimicking phlegmonous myositis: A case report.模仿脓性肌炎的CD30结外自然杀伤/T细胞淋巴瘤:一例报告
Oncol Lett. 2014 May;7(5):1419-1421. doi: 10.3892/ol.2014.1924. Epub 2014 Feb 28.
8
Unusual case of metachronous EBV-associated B-cell and NK/T-cell lymphoma mimicking polymyositis-diagnostic challenges and pitfalls.异时性EB病毒相关B细胞和NK/T细胞淋巴瘤酷似多发性肌炎的罕见病例——诊断挑战与陷阱
Am J Hematol. 2014 Jan;89(1):110-3. doi: 10.1002/ajh.23572. Epub 2013 Oct 15.
9
How I treat NK/T-cell lymphomas.我如何治疗 NK/T 细胞淋巴瘤。
Blood. 2013 Jun 20;121(25):4997-5005. doi: 10.1182/blood-2013-01-453233. Epub 2013 May 7.
10
Clinical differences between nasal and extranasal natural killer/T-cell lymphoma: a study of 136 cases from the International Peripheral T-Cell Lymphoma Project.鼻型与鼻外型自然杀伤/T细胞淋巴瘤的临床差异:一项来自国际外周T细胞淋巴瘤项目的136例病例研究。
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误诊为多发性肌炎的结外自然杀伤/T细胞淋巴瘤的肌肉受累:一例报告并文献复习

Muscular involvement of extranodal natural killer/T cell lymphoma misdiagnosed as polymyositis: A case report and review of literature.

作者信息

Liu Li-Hui, Huang Qing, Liu Yun-Hai, Yang Jie, Fu Han, Jin Lin

机构信息

Department of Neurology, Xiangya Hospital of Central South University, Changsha 410008, Hunan Province, China.

Department of Dermatology, Xiangya Hospital of Central South University, Changsha 410008, Hunan Province, China.

出版信息

World J Clin Cases. 2020 Mar 6;8(5):963-970. doi: 10.12998/wjcc.v8.i5.963.

DOI:10.12998/wjcc.v8.i5.963
PMID:32190634
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7062622/
Abstract

BACKGROUND

Natural killer (NK)/T cell lymphoma is a rare and highly aggressive malignant tumor, and is a special form of non-Hodgkin's lymphoma. Although extranodal involvement is frequently found in tissues such as the skin, testicular and gastrointestinal tract , its presence in skeletal muscle has scarcely been reported in the literature.

CASE SUMMARY

We report a case of extranodal NK/T cell lymphoma with muscle swelling as the first clinical manifestation. A 42-year-old man, who initially presented with localized swelling in the double lower extremities, demonstrated gradual facial and eyelid swelling, and his imaging results showed multiple sites of muscle damage throughout the body. The final pathological results suggested NK/T cell lymphoma, and immunohistochemistry showed CD20 (-), CD3Ɛ (+), CD30 (+), CD56 (-), EBER (+), Ki67 (60%), TIA-1 (+) and CD68 (±) staining. The muscle swelling significantly improved after treatment with chemotherapy regimens.

CONCLUSION

This disease is difficult to diagnose and highly invasive, and should be included in the differential diagnosis of unexplained muscle swelling.

摘要

背景

自然杀伤(NK)/T细胞淋巴瘤是一种罕见且侵袭性很强的恶性肿瘤,是非霍奇金淋巴瘤的一种特殊形式。尽管结外受累常见于皮肤、睾丸和胃肠道等组织,但其在骨骼肌中的存在在文献中鲜有报道。

病例摘要

我们报告一例以肌肉肿胀为首发临床表现的结外NK/T细胞淋巴瘤病例。一名42岁男性,最初表现为双下肢局部肿胀,随后面部和眼睑逐渐肿胀,其影像学检查结果显示全身多处肌肉受损。最终病理结果提示NK/T细胞淋巴瘤,免疫组化显示CD20(-)、CD3Ɛ(+)、CD30(+)、CD56(-)、EBER(+)、Ki67(60%)、TIA-1(+)和CD68(±)染色。化疗方案治疗后肌肉肿胀明显改善。

结论

本病诊断困难且侵袭性强,应列入不明原因肌肉肿胀的鉴别诊断。