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利妥昔单抗治疗人类免疫缺陷病毒相关的杆状体肌病：文献能告诉我们什么？

Rituximab as a treatment for human immunodeficiency virus-associated nemaline myopathy: What does the literature have to tell us?

作者信息

Gonçalves Júnior Jucier, Shinjo Samuel Katsuyuki

机构信息

Division of Rheumatology, São Paulo University, São Paulo 01246-903, Brazil.

出版信息

World J Clin Cases. 2022 Feb 6;10(4):1454-1456. doi: 10.12998/wjcc.v10.i4.1454.

DOI:10.12998/wjcc.v10.i4.1454
PMID:35211583
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8855173/
Abstract

We presented a letter about a case of a 37-year-old Black female with a history of human immunodeficiency virus and an undetectable viral load. She was evaluated with weakness in the scapular (grade III) and pelvic girdles (grade II), elevation of creatine phosphokinase levels and muscle biopsy compatible with nemaline myopathy. She was treated with rituximab showing improvement of the condition.

摘要

我们提交了一封信，内容是关于一名37岁的黑人女性病例，她有人类免疫缺陷病毒病史且病毒载量检测不到。她接受了评估，发现肩胛带肌无力（III级）和骨盆带肌无力（II级），肌酸磷酸激酶水平升高，肌肉活检结果符合杆状体肌病。她接受了利妥昔单抗治疗，病情有所改善。

相似文献

1
Rituximab as a treatment for human immunodeficiency virus-associated nemaline myopathy: What does the literature have to tell us?利妥昔单抗治疗人类免疫缺陷病毒相关的杆状体肌病：文献能告诉我们什么？
World J Clin Cases. 2022 Feb 6;10(4):1454-1456. doi: 10.12998/wjcc.v10.i4.1454.
2
Mild phenotype of nemaline myopathy with sleep hypoventilation due to a mutation in the skeletal muscle alpha-actin (ACTA1) gene.由于骨骼肌α-肌动蛋白（ACTA1）基因突变导致的伴有睡眠低通气的杆状体肌病的轻度表型。
Neuromuscul Disord. 2001 Jan;11(1):35-40. doi: 10.1016/s0960-8966(00)00167-x.
3
Human immunodeficiency virus-associated myopathy: analysis of 11 patients.
Ann Neurol. 1988 Jul;24(1):79-84. doi: 10.1002/ana.410240114.
4
An adult nemaline myopathy patient with respiratory and heart failure harboring a novel variant.一名患有呼吸和心力衰竭的成年杆状体肌病患者携带一种新的变异。
eNeurologicalSci. 2020 Aug 26;21:100268. doi: 10.1016/j.ensci.2020.100268. eCollection 2020 Dec.
5
[An adulthood progressive case of congenital nemaline myopathy showing rimmed vacuoles in muscle biopsy and diffuse neurogenic changes on electromyography].[一例成年期进展性先天性杆状体肌病，肌肉活检显示镶边空泡，肌电图显示弥漫性神经源性改变]
Rinsho Shinkeigaku. 2004 Jul;44(7):450-3.
6
[A comparative study of the clinical and histological characteristics between classic nemaline myopathy and that associated with the human immunodeficiency virus].
Med Clin (Barc). 1995 Oct 21;105(13):500-3.
7
Adult-onset nemaline myopathy: a case report and review of the literature.
Arch Pathol Lab Med. 1997 Nov;121(11):1210-3.
8
[Two adult cases of nemaline myopathy presenting different clinical symptoms and CT findings].
No To Shinkei. 2001 Jul;53(7):653-8.
9
[Nemaline rod myopathy treated with L-tyrosine to relieve symptoms in a neonate].[用L-酪氨酸治疗新生儿杆状体肌病以缓解症状]
Arch Argent Pediatr. 2019 Aug 1;117(4):e382-e386. doi: 10.5546/aap.2019.e386.
10
Identification of a novel nemaline myopathy-causing mutation in the troponin T1 (TNNT1) gene: a case outside of the old order Amish.肌钙蛋白T1（TNNT1）基因中一个导致杆状体肌病的新突变的鉴定：一例非旧秩序阿米什人的病例。
Muscle Nerve. 2015 May;51(5):767-72. doi: 10.1002/mus.24528. Epub 2015 Feb 17.

本文引用的文献

1
Nemaline myopathy with dilated cardiomyopathy and severe heart failure: A case report.伴有扩张型心肌病和严重心力衰竭的杆状体肌病：一例报告。
World J Clin Cases. 2021 Apr 16;9(11):2569-2575. doi: 10.12998/wjcc.v9.i11.2569.
2
Sporadic late-onset nemaline myopathy: a case report of a treatable cause of cardiac failure.散发性迟发性杆状体肌病：一例心力衰竭可治疗病因的病例报告。
Eur Heart J Case Rep. 2020 Dec 22;5(1):ytaa480. doi: 10.1093/ehjcr/ytaa480. eCollection 2021 Jan.
3
Sporadic late-onset nemaline myopathy with monoclonal gammopathy of undetermined significance: Report of four patients.散发型迟发性杆状体肌病伴意义未明的单克隆丙种球蛋白血症：4 例报告。
Neuromuscul Disord. 2021 Jan;31(1):29-34. doi: 10.1016/j.nmd.2020.11.004. Epub 2020 Nov 12.
4
Sporadic late-onset nemaline myopathy: Clinical spectrum, survival, and treatment outcomes.散发性晚发性杆状体肌病：临床谱、生存和治疗结果。
Neurology. 2019 Jul 16;93(3):e298-e305. doi: 10.1212/WNL.0000000000007777. Epub 2019 Jun 5.
5
Sporadic late-onset nemaline myopathy with monoclonal gammopathy of undetermined significance (SLONM-MGUS): An alternative treatment using cyclophosphamide-thalidomide-dexamethasone (CTD) regimen.散发型迟发性肌病伴意义未明的单克隆丙种球蛋白血症（SLONM-MGUS）：使用环磷酰胺-沙利度胺-地塞米松（CTD）方案的一种替代治疗方法。
Neuromuscul Disord. 2018 Jul;28(7):610-613. doi: 10.1016/j.nmd.2018.04.011. Epub 2018 May 16.
6
Sporadic late-onset nemaline myopathy: clinico-pathological characteristics and review of 76 cases.散发性迟发性杆状体肌病：76例临床病理特征及文献复习
Orphanet J Rare Dis. 2017 May 11;12(1):86. doi: 10.1186/s13023-017-0640-2.
7
Review of Cardiac Disease in Nemaline Myopathy.杆状体肌病中心脏疾病的综述
Pediatr Neurol. 2015 Dec;53(6):473-7. doi: 10.1016/j.pediatrneurol.2015.08.014. Epub 2015 Aug 28.
8
Effects of rituximab in two patients with dysferlin-deficient muscular dystrophy.利妥昔单抗治疗两例肌营养不良症患者的效果。
BMC Musculoskelet Disord. 2010 Jul 11;11:157. doi: 10.1186/1471-2474-11-157.