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肿块:脊柱中的难题。

Mass: The Conundrum in Spine.

作者信息

Rath P D, Katoch Sunil, Agrawal Abhijeet Kumar, Chouhan Swetal, Bajaj H N, Bisaralli Rahul

机构信息

Department of Rheumatology, Max Healthcare, Saket, New Delhi, India.

Department of Spine Surgery, Max Healthcare, Saket, New Delhi, India.

出版信息

J Orthop Case Rep. 2023 Apr;13(4):37-40. doi: 10.13107/jocr.2023.v13.i04.3606.

Abstract

INTRODUCTION

Immunoglobulin (Ig)G4-related disease belongs to a rare compilation of conditions in rheumatology and may involve a multitude of organs. Amidst the central nervous system (CNS) presentation, involvement of spinal cord is rarer still.

CASE REPORT

Case 1: A 50-year-old male came with chief complaints of tingling sensation over both soles since 2 months associated with lower back ache and gait disturbance in the form of spastic gait. X-rays of spine were suggestive of a growth at the level of D10-D12 compressing the spinal cord with no focal sclerotic/lytic lesions, and MRI dorsolumbar spine showed dural tail sign. The patient underwent excision of dural mass, and histopathology revealed majority of plasma cells positive for IgG4. Case 2: A 65-year-old female came with complaints of cough, shortness of breath, and fever on and off since 2 months. No history of hemoptysis, purulent sputum, weight loss. On examination: There were bilateral rhonchi in the left upper zone. MRI spine showed focal erosion with soft-tissue thickening at the right paravertebral region extending from D5-9. The patient underwent surgery (fusion D6-8 and ostectomy D7 posterior rib resection D7 right side) with the right pleural biopsy and transpendicular intracorporal biopsy D7. Histopathology was compatible with findings of IgG4 disease.

CONCLUSION

IgG4 tumors presenting in CNS itself is rare and rarer in spinal cord. Histopathological examination is central to diagnose and prognosticate the disease further as IgG4-related disease manifestations may recur without proper treatment.

摘要

引言

免疫球蛋白(Ig)G4相关疾病属于风湿病学中罕见的病症集合,可能累及多个器官。在中枢神经系统(CNS)表现中,脊髓受累更为罕见。

病例报告

病例1:一名50岁男性,自2个月以来主要抱怨双足底有刺痛感,并伴有下背部疼痛以及痉挛性步态形式的步态障碍。脊柱X线提示在D10 - D12水平有一个肿物压迫脊髓,无局灶性硬化/溶骨性病变,胸腰椎MRI显示硬膜尾征。患者接受了硬膜肿物切除术,组织病理学显示大多数浆细胞IgG4阳性。病例2:一名65岁女性,自2个月以来断断续续出现咳嗽、气短和发热。无咯血、脓性痰、体重减轻病史。检查:左上肺区有双侧啰音。脊柱MRI显示右侧椎旁区域从D5 - 9有局灶性侵蚀伴软组织增厚。患者接受了手术(D6 - 8融合术、D7椎板切除术、右侧第7后肋切除术)以及右侧胸膜活检和D7经椎弓根体内活检。组织病理学与IgG4疾病的表现相符。

结论

IgG4肿瘤在中枢神经系统本身就很罕见,在脊髓中更为罕见。组织病理学检查对于进一步诊断和预测该疾病至关重要,因为如果没有适当治疗,IgG4相关疾病表现可能会复发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd8f/10182585/3bf944c9f151/JOCR-13-37-g001.jpg

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