A rare case report of neurolymphomatosis with NK-T-cell lymphoma

Ruta Savaj, Megha Harke Uppin, Megha Dhamne
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Abstract

Neurolymphomatosis (NL) is a rare entity. It is usually a manifestation of B-cell lymphoma. Here we describe a case of neurolymphomatosis in a 72 year old man who was in remission for Nasal T-cell lymphoma and presented to us with subacute onset painful mononeuritis like weakness involving all 4 limbs sequentially over a period of 4 months. he was initially treated as CIDP with steroids but later in view of progression he was evaluated further. His FDG PET-CT showed increased uptake in left brachial plexus which was confirmed by subsequent MRI neurography. He underwent biopsy of left brachial plexus and diagnosis of neurolymphomatosis was confirmed. He was treated with intravenous immunoglobulins (2 gm/kg) over 5 days with minimal improvement in his neurological symptoms, his shoulder pain improved and he could feed himself with right hand. He was offered palliative treatment in view of poor prognosis seen in neurolymphomatosis. He succumbed to the illness 3 months later.
神经淋巴瘤合并nk - t细胞淋巴瘤1例
神经淋巴瘤(NL)是一种罕见的疾病。它通常是b细胞淋巴瘤的表现。在这里,我们描述了一个72岁的神经淋巴瘤患者,他的鼻t细胞淋巴瘤处于缓解期,向我们提出了亚急性发作的疼痛性单神经炎,如四肢无力,持续4个月。他最初接受类固醇治疗,但后来鉴于病情进展,对他进行了进一步评估。他的FDG PET-CT显示左臂丛摄取增加,随后的MRI神经造影证实了这一点。他接受了左臂丛活检,确诊为神经淋巴瘤。患者接受静脉注射免疫球蛋白(2 gm/kg)治疗5天,其神经症状改善甚微,肩部疼痛得到改善,并能用右手进食。鉴于神经淋巴瘤预后不良,给予姑息治疗。3个月后他病逝了。
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