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葡萄膜炎和肌炎作为难治性NK/T细胞鼻型淋巴瘤免疫并发症经异基因干细胞移植成功治疗

Uveitis and Myositis as Immune Complications in Chemorefractory NK/T-Cell Nasal-Type Lymphoma Successfully Treated with Allogeneic Stem-Cell Transplant.

作者信息

Gómez-Crespo Maria José, García-Raso Aránzazu, López-Lorenzo Jose Luis, Villaescusa Teresa, Rodríguez-Pinilla María, Fortes José, Serrano Cristina, Machan Salma, Llamas Pilar, Córdoba Raúl

机构信息

Lymphoma Unit, Department of Hematology, Fundación Jiménez Díaz University Hospital, Health Research Institute IIS-FJD, Madrid, Spain.

Department of Pathology, Fundación Jiménez Díaz University Hospital, Health Research Institute IIS-FJD, Madrid, Spain.

出版信息

Case Rep Hematol. 2016;2016:7297920. doi: 10.1155/2016/7297920. Epub 2016 Oct 11.

Abstract

NK/T-cell lymphomas are a group of clonal proliferations of NK- or, rarely, T-cell types and have peculiar clinicopathologic features. Most common site of involvement is the upper aerodigestive tract (nasal cavity, nasopharynx, paranasal sinuses, and palate). Association of autoimmune paraneoplastic disorders with NK/T-cell lymphomas is not well studied. Our patient was diagnosed with NK/T-cell lymphoma stage IV with skin involvement and treated frontline with CHOEP regimen. While he was under treatment, two immune complications presented: anterior uveitis of autoimmune origin refractory to steroids and myositis in lower limbs muscles. Autologous transplantation was rejected due to confirmed early relapse after first-line treatment, and the patient received second-line treatment according to the SMILE scheme, reaching complete response after four cycles. The patient underwent allogeneic transplantation and at the time of manuscript preparation is alive despite multiple complications. The disease should be suspected in patients with rhinitis or recurrent sinusitis, and early biopsy is recommended for all patients to avoid a delay in diagnosis. Our patient also presented symptoms of disease progression after first-line treatment, representing a paraneoplastic process, a very rare phenomenon in T-type lymphomas. This case is novel for the appearance of an inflammatory myositis, a histologically verified paraneoplastic phenomenon that responded to treatment for lymphoma.

摘要

NK/T细胞淋巴瘤是一组自然杀伤(NK)细胞或罕见的T细胞类型的克隆性增殖疾病,具有独特的临床病理特征。最常累及的部位是上消化道(鼻腔、鼻咽、鼻窦和腭部)。自身免疫性副肿瘤性疾病与NK/T细胞淋巴瘤的关联尚未得到充分研究。我们的患者被诊断为IV期NK/T细胞淋巴瘤伴皮肤受累,并接受了一线CHOEP方案治疗。在治疗期间,出现了两种免疫并发症:对类固醇难治的自身免疫性前葡萄膜炎和下肢肌肉的肌炎。由于一线治疗后确诊早期复发,自体移植被拒绝,患者根据SMILE方案接受二线治疗,四个周期后达到完全缓解。患者接受了异基因移植,在撰写本文时,尽管有多种并发症,但仍然存活。对于患有鼻炎或复发性鼻窦炎的患者应怀疑该病,建议所有患者尽早进行活检以避免诊断延误。我们的患者在一线治疗后也出现了疾病进展的症状,表现为一种副肿瘤过程,这在T型淋巴瘤中是一种非常罕见的现象。该病例的新颖之处在于出现了炎性肌炎,这是一种经组织学证实的对淋巴瘤治疗有反应的副肿瘤现象。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/498b/5078671/2f96274d4ed4/CRIHEM2016-7297920.001.jpg

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