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成人斯蒂尔病作为急性髓系白血病的首发表现:一例病例报告

Adult-onset Still's disease as the first manifestation of acute myeloid leukemia: a case report.

作者信息

Ibrahim Ranim, Drie Tasneem, Shahada Zienab, Al Halabi Hayat, Kudsi Maysoun

机构信息

Department of Rheumatology, Al-Mouwasat University Hospital.

Departmen of Rheumatology, Damascus University/Syrian Private University, Damascus, Syria.

出版信息

Ann Med Surg (Lond). 2023 Feb 17;85(3):532-535. doi: 10.1097/MS9.0000000000000256. eCollection 2023 Mar.

DOI:10.1097/MS9.0000000000000256
PMID:36923783
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10010820/
Abstract

UNLABELLED

The association between adult-onset Still's disease (AOSD) and malignancy has previously been observed. However, only a limited number of cases described a combination of AOSD and leukemia, none of which reported AOSD-related symptoms as the first manifestation of acute myeloid leukemia (AML). This presentation might represent a paraneoplastic syndrome or leukemic arthritis mimicking AOSD.

CASE PRESENTATION

Here the authors report a case of a 23-year-old female who fulfilled the Yamaguchi criteria for an AOSD diagnosis. She presented with complaints of polyarthritis, sore throat, and daily fever spikes with the appearance of a nonpruritic maculopapular salmon-colored rash. Her laboratory work showed marked pancytopenia, which led to a bone marrow examination and an AML diagnosis. The patient started receiving chemotherapy with considerable improvement in the AOSD-related symptoms.

CLINICAL DISCUSSION

Patients with underlying malignancies could present with systemic features compatible with AOSD, which necessitates excluding malignancy in any patient with this presentation, specifically in light of some warning signs like pancytopenia.

CONCLUSION

This case interprets a rare association between AOSD and AML. In addition, it highlights how crucial it is to be aware of the signs that should warn the clinician of a possible underlying malignancy in any patient presenting with AOSD-related symptoms.

摘要

未标注

此前已观察到成人斯蒂尔病(AOSD)与恶性肿瘤之间的关联。然而,仅有少数病例描述了AOSD与白血病的合并情况,其中无一例报告AOSD相关症状为急性髓系白血病(AML)的首发表现。这种表现可能代表一种副肿瘤综合征或类似AOSD的白血病性关节炎。

病例报告

本文作者报告一例23岁女性病例,该病例符合AOSD诊断的山口标准。她主诉多关节炎、咽痛,每日发热高峰时出现非瘙痒性斑丘疹样鲑鱼色皮疹。她的实验室检查显示明显全血细胞减少,这导致进行骨髓检查并诊断为AML。患者开始接受化疗,AOSD相关症状有显著改善。

临床讨论

潜在恶性肿瘤患者可能出现与AOSD相符的全身特征,这就需要在任何有此表现的患者中排除恶性肿瘤,特别是鉴于一些警示信号如全血细胞减少。

结论

该病例诠释了AOSD与AML之间罕见的关联。此外,它凸显了对于任何出现AOSD相关症状的患者,意识到那些应警示临床医生可能存在潜在恶性肿瘤的体征是多么关键。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54d0/10010820/dc6c8427df23/ms9-85-579-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54d0/10010820/dc6c8427df23/ms9-85-579-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54d0/10010820/dc6c8427df23/ms9-85-579-g001.jpg

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