Sarcoidosis in Close Family Members and Susceptibility to High Grade B-Cell Lymphoma: A Case Report Study

Hana Magrooni, N. Javadian, Ghasem Farahmand, Sakineh Ranji-Burachaloo
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Abstract

The presented case is an 81- year-old woman who had experienced episodes of facial twitching without loss of consciousness and flu like symptoms for a few weeks prior to her admission. examinations were unremarkable except for left 3rd nerve and right 6th nerve palsy, right peripheral facial palsy and right -side hemiparesis. FH was positive for sarcoidosis. neuroimaging were in favor of PCNSL. Sarcoidosis and malignancy maybe etiologically related in at least 25% of cases. Coexis- tence of sarcoidosis and lymphoma have been reported previously. Our patient had two daughters with sarcoidosis and her chest CT scan showed multiple lymph nodes inmedias- tinum. Unfortunately, due to the location and the technical restriction, biopsy of mediasti- nal lymph nodes was not performedfor our patient and we could not differentiate whether it was reactive, paraneoplastic or granulomatous. We present this case as concurrence of lymphoma and sarcoidosis in a family, which could guide a new concern for the patient with granulomatous infiltrative disease for early diagnosis and familial screening.
近亲属结节病与高级别b细胞淋巴瘤易感性:一个病例报告研究
该病例是一名81岁的女性,在入院前的几周内,她经历了面部抽搐,没有失去意识和流感样症状。除左侧第3神经和右侧第6神经麻痹、右侧周围性面瘫和右侧偏瘫外,其余检查均无异常。FH结节病阳性。神经影像学检查有利于PCNSL。结节病和恶性肿瘤可能在至少25%的病例中与病因有关。结节病和淋巴瘤的并发症已有报道。我们的病人有两个女儿患有结节病,她的胸部CT扫描显示中间有多个淋巴结。不幸的是,由于位置和技术限制,我们的患者没有进行中间淋巴结活检,我们无法区分它是反应性的、副肿瘤性的还是肉芽肿性的。我们将该病例描述为淋巴瘤和结节病在一个家族中同时发生,这可能为肉芽肿性浸润性疾病患者的早期诊断和家族筛查提供新的关注点。
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