椎板Lucida型线性IgA病并发结肠息肉病和直肠腺癌1例。

IF 0.9 Q4 DERMATOLOGY Case Reports in Dermatology Pub Date : 2023-09-01 eCollection Date: 2023-01-01 DOI:10.1159/000532104
Akiko Miyazaki, Saori Itoi-Ochi, Mami Hayashi, Asako Ota, Kengo Nagai, Shinya Inoue, Naohiro Tomita, Hidetaka Eguchi, Yasushi Okazaki, Hideyuki Ishida, Takashi Hashimoto
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摘要

线性IgA病(LAD)是一种罕见的自身免疫性大疱性疾病,其特征是IgA沉积在基底膜区(BMZ)。一位66岁的男性因骨髓增生异常综合征在我院接受了5年的治疗,在此期间他的病情保持稳定。他因红斑伴瘙痒而来我科就诊,这种情况在1年前出现,并随着水泡和糜烂的发展而逐渐加剧。在第一次就诊期间,在躯干和下肢上观察到多处红斑,周围有侵蚀和结皮。组织病理学检查显示表皮下水疱伴炎性细胞浸润,主要由中性粒细胞、嗜酸性粒细胞和淋巴细胞组成。直接和间接免疫荧光分别在BMZ和IgA抗BMZ抗体中显示线性IgA沉积,而使用HaCaT细胞的浓缩培养上清液的免疫印迹检测到对120kDa LAD-1反应的IgA抗体。因此,患者被诊断为透明层型LAD。随后的结肠镜检查显示多发性结肠息肉和直肠腺癌(Tis、N0和M0)。多基因小组试验显示ATM变异具有未知意义,但未检测到任何与肠息肉病综合征相关的致病变异。口服50毫克/天的黄砜,切除结肠息肉和腺癌,皮肤病变迅速消退。据我们所知,这是第一例LAD合并多发性结直肠息肉和直肠腺癌的报道。此外,我们还分析了文献中报道的LAD与恶性肿瘤相关的病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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A Case of Lamina Lucida-Type Linear IgA Disease Complicated by Colon Polyposis and Rectal Adenocarcinoma.

Linear IgA disease (LAD) is a rare autoimmune bullous disease characterized by IgA deposition in the basement membrane zone (BMZ). A 66-year-old male was treated for myelodysplastic syndrome at our hospital for 5 years, during which his condition remained stable. He visited our department because of erythema with itching, which appeared 1 year ago and gradually exacerbated with the development of blisters and erosions. During the first visit, multiple erythemas with erosions and crusts on their periphery were observed on the trunk and lower limbs. Histopathological examination revealed subepidermal blisters with inflammatory cell infiltration, mainly constituting of neutrophils, eosinophils, and lymphocytes. Direct and indirect immunofluorescence showed linear IgA deposits in the BMZ and IgA anti-BMZ antibodies, respectively, while immunoblotting using a concentrated culture supernatant of HaCaT cells detected IgA antibodies reactive to 120-kDa LAD-1. Accordingly, the patient was diagnosed with lamina lucida-type LAD. Subsequent colonoscopy revealed multiple colorectal polyps and rectal adenocarcinoma (Tis, N0, and M0). Multigene panel test showed an ATM variant of unknown significance but did not detect any pathogenic variants associated with intestinal polyposis syndrome. The skin lesions quickly resolved with oral diaphenylsulfone 50 mg/day and resection of the colorectal polyps and adenocarcinoma. To our knowledge, this is the first reported case of LAD associated with multiple colorectal polyps and rectal adenocarcinoma. Additionally, we also analyzed reported cases of LAD associated with malignancy from the literature.

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来源期刊
CiteScore
1.60
自引率
0.00%
发文量
57
审稿时长
9 weeks
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