Primary neurolymphomatosis presenting as foot drop: A rare case report

被引:0
|
作者
Bakshi, Neha [1 ]
Chand, Vineeta [2 ]
Anand, Rajiv [3 ]
Duggal, Rajan [2 ]
机构
[1] Sir Ganga Ram Hosp, Dept Pathol, Histopathol Div, New Delhi, India
[2] BLK MAX Hosp, Dept Histopathol & Cytopathol, Pusa Rd, New Delhi, India
[3] BLK MAX Hosp, Dept Neurol, New Delhi, India
关键词
Diagnosis; lymphoma; management; neuropathy; peripheral nervous system; LYMPHOMA; NEUROPATHY; DIAGNOSIS;
D O I
10.4103/ijpm.ijpm_731_22
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Neurolymphomatosis (NL) is the direct infiltration of the peripheral nervous system (PNS) by lymphoma cells and represents the least common form of PNS involvement by lymphoma. Clinical presentation is varied, and early diagnosis remains challenging. Nerve biopsy remains the diagnostic gold standard, use of magnetic resonance imaging (MRI) and fluorodeoxyglucose-positron emission tomography (FDG-PET) may help in diagnosis and selecting targets for biopsy. We report an account of an older male patient who presented with subacute onset multifocal neuropathy involving bilateral lower limbs and left foot drop. The patient was initially misdiagnosed as chronic inflammatory demyelinating polyneuropathy; however radiological assessment revealed fusiform thickening of the L5 nerve root and biopsy from the site revealed extensive infiltration by diffuse large B cell type non-Hodgkin lymphoma (NHL). High index of suspicion is vital to ensure correct diagnosis, timely treatment, and to improve patient survival.
引用
收藏
页码:918 / 920
页数:3
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