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<编辑精选>伴 8 号三体周期性发热和 10 号外显子以外多个基因突变的骨髓增生异常综合征:病例报告。

<Editors' Choice> Myelodysplastic syndrome with trisomy 8 presenting periodic fever and multiple gene variants outside exon 10: a case report.

机构信息

Department of Education for Community-Oriented Medicine, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Department of General Medicine, Nagoya University Hospital, Nagoya, Japan.

出版信息

Nagoya J Med Sci. 2023 Feb;85(1):195-203. doi: 10.18999/nagjms.85.1.195.

Abstract

Myelodysplastic syndrome is associated with the development of autoinflammatory conditions, such as recurrent fever, polymyalgia, arthralgia, and erythema. Trisomy 8 is a common chromosomal abnormality in patients with myelodysplastic syndrome. Myelodysplastic syndrome with trisomy 8 involves autoinflammatory conditions, especially Behet's disease-like symptoms with intestinal mucosal damage. variants, particularly those in exon 10, are pathogenic in familial Mediterranean fever, the most common autoinflammatory disease, presenting typical symptoms such as periodic fever and pleuritis/pericarditis/peritonitis. variants outside exon 10 are common in Japanese patients with familial Mediterranean fever and are associated with atypical symptoms, including myalgia and erythema. variants in myelodysplastic syndrome with trisomy 8 have rarely been investigated, although myelodysplastic syndrome with trisomy 8 might develop autoinflammatory conditions similar to those in familial Mediterranean fever. We encountered a 67-year-old man who had myelodysplastic syndrome with trisomy 8 and multiple variants outside exon 10. He presented with periodic fever, as well as chest/abdominal pain, myalgia, and erythema, although the symptoms did not fulfill the diagnostic criteria of familial Mediterranean fever. We discussed the possibility that these symptoms are modified by variants outside exon 10 in myelodysplastic syndrome with trisomy 8.

摘要

骨髓增生异常综合征与自身炎症性疾病的发展有关,如复发性发热、巨细胞性多肌痛、关节炎和红斑。8 三体是骨髓增生异常综合征患者常见的染色体异常。伴有 8 三体的骨髓增生异常综合征涉及自身炎症性疾病,特别是伴有肠黏膜损伤的贝赫切特病样症状。10 号外显子中的 变体在家族性地中海热中是致病的,家族性地中海热是最常见的自身炎症性疾病,表现为周期性发热和胸膜炎/心包炎/腹膜炎。10 号外显子以外的 变体在日本的家族性地中海热患者中很常见,与非典型症状相关,包括肌痛和红斑。伴有 8 三体的骨髓增生异常综合征中的 变体很少被研究,尽管伴有 8 三体的骨髓增生异常综合征可能会出现类似于家族性地中海热的自身炎症性疾病。我们遇到了一位 67 岁的男性,他患有伴有 8 三体的骨髓增生异常综合征和多个 10 号外显子以外的 变体。他表现为周期性发热,以及胸痛/腹痛、肌痛和红斑,尽管这些症状不符合家族性地中海热的诊断标准。我们讨论了这些症状可能是由伴有 8 三体的骨髓增生异常综合征中的 10 号外显子以外的 变体修饰的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eada/10009629/883d9c2c3340/2186-3326-85-0195-g001.jpg

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