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Hepatosplenic T-Cell Lymphoma: A Rare Complication of Monotherapy with Thiopurines in Crohns Disease

机译:肝脾性T细胞淋巴瘤:克罗恩病硫嘌呤单一疗法的罕见并发症

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摘要

Hepatosplenic T-cell lymphoma (HSTCL) is an extremely rare and aggressive form of non-Hodgkin lymphoma associated with poor response to treatment and high mortality. There is an increased incidence among patients with inflammatory bowel disease, especially young male patients under 35 years old and on combination therapy (thiopurine and anti-TNF-α). We describe a case of HSTCL in a young male patient with stenosing ileal Crohn's disease on azathioprine monotherapy for 4.8 years admitted to our hospital with intra- abdominal sepsis. Despite chemotherapy, the patient eventually died 1 month after the diagnosis. Through a literature review, we identified 18 additional cases of HSTCL in Crohn's disease patients that had only been treated with thiopurine monotherapy. The authors intend to highlight the rarity of this diagnosis especially with azathioprine monotherapy and the diagnostic challenge in a case that presented with intra-abdominal sepsis.
机译:肝脾T细胞淋巴瘤(HSTCL)是一种非霍奇金淋巴瘤,极为罕见且侵袭性,与治疗反应差,死亡率高有关。在炎症性肠病患者中,尤其是在35岁以下且接受联合治疗(硫嘌呤和抗TNF-α)的年轻男性患者中,发病率增加。我们描述了一名年轻男性男性患者在接受硫唑嘌呤单药治疗的狭窄性回肠克罗恩氏病4.8年的HSTCL病例,该患者入院腹腔内败血症。尽管进行了化疗,该患者最终在诊断后1个月死亡。通过文献综述,我们在仅用硫嘌呤单一疗法治疗的克罗恩病患者中发现了另外18例HSTCL病例。作者打算强调这种诊断的罕见性,尤其是硫唑嘌呤单药治疗,以及腹内脓毒症患者的诊断挑战。

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