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重症肌无力揭示霍奇金淋巴瘤

Myasthenia Gravis Revealing Hodgkin's Lymphoma.

作者信息

Yousfi Jaouad, Bensalek Fatimazahra, Zahlane Mouna, Benjilali Laila, Essaadouni Lamiaa

机构信息

University Hospital of Mohammed VI, Department of Internal Medicine, Marrakesh, Morocco.

出版信息

Eur J Case Rep Intern Med. 2021 Mar 12;8(3):002375. doi: 10.12890/2021_002375. eCollection 2021.

Abstract

INTRODUCTION

Myasthenia gravis is a rare autoimmune disease caused by autoantibodies directed against the synapses of the neuromuscular junction.

PATIENT AND METHODS

We report the case of a young patient with myasthenia gravis associated with Hodgkin's lymphoma.

RESULTS

A 22-year-old patient presented with a 2-month history of severe weakness associated with muscle fatigability and intermittent ptosis without dysphonia or respiratory signs. Clinical examination revealed generalized myasthenia. The EMG did not show post-synaptic block, and anti-acetylcholine receptor antibodies were elevated at 3 nmol/l (normal ≤0.3 nmol/l). CT of the thorax showed an anterior medial mass. Immunohistochemistry of the mass revealed mixed cellularity Hodgkin's lymphoma.

CONCLUSION

The association of lymphomas with myasthenia gravis has been rarely reported.

LEARNING POINTS

Myasthenia gravis is an autoimmune disease of the neuromuscular junction and can be associated with malignant haemopathy.The coexistence of myasthenia and Hodgkin's lymphoma is very rare.This association is a therapeutic challenge.

摘要

引言

重症肌无力是一种罕见的自身免疫性疾病,由针对神经肌肉接头突触的自身抗体引起。

患者与方法

我们报告了一例患有重症肌无力并伴有霍奇金淋巴瘤的年轻患者的病例。

结果

一名22岁患者有2个月严重肌无力病史,伴有肌肉疲劳和间歇性上睑下垂,无声音嘶哑或呼吸症状。临床检查发现全身性重症肌无力。肌电图未显示突触后阻滞,抗乙酰胆碱受体抗体升高至3 nmol/l(正常≤0.3 nmol/l)。胸部CT显示前内侧肿块。肿块的免疫组织化学检查显示为混合细胞型霍奇金淋巴瘤。

结论

淋巴瘤与重症肌无力的关联鲜有报道。

学习要点

重症肌无力是一种神经肌肉接头的自身免疫性疾病,可与恶性血液病相关。重症肌无力与霍奇金淋巴瘤并存非常罕见。这种关联是一个治疗挑战。

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