Primary Central Nervous System Lymphoma in an Immunocompetent Young Adult Patient: A Rare Case.

IF 0.7 Q3 MEDICINE, GENERAL & INTERNAL
Acta medica Indonesiana Pub Date : 2023-01-01
Aisyah Wirdah, Norman Djamaludin, Mediarty Syahrir, Yenny Dian Andayani, Mita Andriani, Yunni Diansari
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引用次数: 0

Abstract

Primary CNS Lymphoma (PCNSL) is a rare form aggressive extra nodal     non-Hodgkin Lymphoma (NHL) that comprising 1-2% of the primary brain tumors that develops in the brain, spinal cord, eye or leptomeningeal area without evidence of systemic involvement. The overall incidence of PCNSL with immunocompetent patients is only 0,47/100.000 year in PCNSL. Approximately 10-20% of patients have ocular involvement and around one third have multifocal neurological disease. Overall long-term survival rate only 20-40%, this is because the management of PCNSL is limited to ability of the drug due to cross the blood brain barrier (BBB). We present a B-cell central nervous system lymphoma in an immunocompetent patient who treat responses with chemotherapy.          A 35-year-old man presented to our hospital with suddenly unconscious 4 hours before admission. He was experiencing headache and blurred of vision withing 3 months and have episode seizure. On Examination, GCS E2 M3 Aphasia, Hemiparesis dextra, papil edema, VOD/VOS: NLP. The other physical exam was normal. Laboratory tests  Hb 10,7 g/dl, LDH 446 U/L, and D-dimer 3,21ug/ml.  Rubella IgG 76,9, CMV Ig G 245,6 and, HSV IgG and IgM negative, HIV test non-reactive, Toxoplasma IgG and Toxoplasma IgM negative, HbsAg and HCV test negative. Brain MRI and MRI Spectroscopy: Lobulated mass size 7,08 cm x 4,75 cm at caudates nucleus sinistra-periventricular lateralis sinistra, Cholin/NAA ratio: 5-9, Cholin/Creatin ration 6-11 suspect malignancy dd/Lymphoma. MRI whole spine: Bulging discus intervertebral C4-C5. Chest and Abdomen CT-Scan are normal. Bone Survey normal, EEG: Epileproform left temporal. Cerebrospinal Fluid: Gliosis reaction sup malignancy.The patient underwent craniotomy and biopsy Pathology Anatomy and IHC Basal Ganglia revealed a Diffuse Large B Cell Lymphoma (NHL) Non-Germinal Center, CD 20 +, Ki 67 95% (High Grade), CD 45 +, CD 3 -, BCL6 +, Mum 1+. The patient we give induction therapy with RMP Regimens (Rituximab 375 mg/m2, day 1, 15 and 29, High Dose Methotrexate (HDMTX) 3000mg/m2 day 2, 16 and 30, and Procarbazine 60mg/m2 day 3-12) because Procarbazine in not available in Palembang we change to Dacarbazine 375mg/m2 days 3,17 and 31), Dexamethasone 5mg/6 hours, and has finished  Low Dose Whole Brain Radiotherapy for consolation therapy. PCNSL is rare form aggressive extra nodal NHL, especially in Immunocompetent patient. In this particular case of patients High Dose Methotrexate Chemotherapy has achieved high respond especially for this patient that showed GCS E4M5V6 and recovery neurological deficit after 2 cycle chemotherapy.

原发性中枢神经系统淋巴瘤在免疫能力的年轻成人患者:一个罕见的病例。
原发性中枢神经系统淋巴瘤(PCNSL)是一种罕见的侵袭性淋巴结外非霍奇金淋巴瘤(NHL),占原发性脑肿瘤的1-2%,发生在脑、脊髓、眼睛或脑膜轻脑膜区,无全身累及的证据。在PCNSL中,免疫功能正常患者的总发病率仅为0.47 /100.000年。约10-20%的患者眼部受累,约三分之一的患者患有多灶性神经系统疾病。总体长期生存率仅为20-40%,这是因为PCNSL的治疗受限于药物通过血脑屏障(BBB)的能力。我们提出一个b细胞中枢神经系统淋巴瘤在免疫能力的病人谁治疗反应化疗。一名35岁男性在入院前4小时突然失去意识。他在3个月内出现头痛和视力模糊,并有癫痫发作。检查GCS E2 M3失语、偏瘫、乳头水肿、VOD/VOS: NLP。另一次体检都正常。实验室检测Hb 10.7 g/dl, LDH 446 U/L, d -二聚体3.21 ug/ml。风疹IgG 76、9,巨细胞病毒IgG 245、6和,HSV IgG和IgM阴性,HIV检测无反应,弓形虫IgG和IgM阴性,HbsAg和HCV检测阴性。脑MRI及MRI谱图:尾状窦核-室旁窦侧分叶状肿块大小7,08 cm x 4,75 cm,胆碱/NAA比值:5-9,胆碱/Creatin比值6-11,怀疑恶性dd/淋巴瘤。全脊柱MRI: C4-C5椎间盘状突起。胸部和腹部ct扫描正常。骨检查正常,脑电图:左颞呈癫痫样。脑脊液:恶性胶质瘤反应。患者行开颅和活检病理解剖及基底节区免疫组化检查显示弥漫性大B细胞淋巴瘤(NHL)非生发中心,cd20 +, Ki 67 95%(高级别),cd45 +, cd3 -, BCL6 +, Mum 1+。我们给予患者RMP方案诱导治疗(利妥昔单抗375mg/m2,第1、15和29天,高剂量甲氨蝶呤(HDMTX) 3000mg/m2,第2、16和30天,丙卡巴嗪60mg/m2,第3-12天),因为巨港没有丙卡巴嗪,我们改为达卡巴嗪375mg/m2,第3、17和31天),地塞米松5mg/6小时,并完成了低剂量全脑放疗进行安慰治疗。PCNSL是一种罕见的侵袭性淋巴结外NHL,尤其见于免疫功能正常的患者。在这个特殊的病例中,高剂量甲氨蝶呤化疗取得了很高的疗效,特别是该患者在2个周期化疗后出现了GCS E4M5V6和恢复神经功能缺陷。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Acta medica Indonesiana
Acta medica Indonesiana MEDICINE, GENERAL & INTERNAL-
CiteScore
2.30
自引率
0.00%
发文量
61
审稿时长
12 weeks
期刊介绍: Acta Medica Indonesiana – The Indonesian Journal of Internal Medicine is an open accessed online journal and comprehensive peer-reviewed medical journal published by the Indonesian Society of Internal Medicine since 1968. Our main mission is to encourage the novel and important science in the clinical area in internal medicine. We welcome authors for original articles (research), review articles, interesting case reports, special articles, clinical practices, and medical illustrations that focus on the clinical area of internal medicine. Subjects suitable for publication include, but are not limited to the following fields of: -Allergy and immunology -Emergency medicine -Cancer and stem cells -Cardiovascular -Endocrinology and Metabolism -Gastroenterology -Gerontology -Hematology -Hepatology -Tropical and Infectious Disease -Virology -Internal medicine -Psychosomatic -Pulmonology -Rheumatology -Renal and Hypertension -Thyroid
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