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Int Cancer Conf J. 2024 Jan 25;13(2):111-118. doi: 10.1007/s13691-023-00646-2. eCollection 2024 Apr.
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本文引用的文献

1
Dermatomyositis following Biosimilar Trastuzumab in a Breast Cancer Patient: A Case Report.一名乳腺癌患者使用生物类似药曲妥珠单抗后发生皮肌炎:病例报告
Case Rep Oncol. 2021 Jul 19;14(2):1134-1138. doi: 10.1159/000517819. eCollection 2021 May-Aug.
2
A Case of Pathological Complete Response and Resolution of Dermatomyositis Following Neoadjuvant Chemotherapy in HER2-Positive Early Breast Cancer.HER2 阳性早期乳腺癌新辅助化疗后病理完全缓解及皮肌炎消退 1 例报告
Curr Oncol. 2021 May 24;28(3):1957-1961. doi: 10.3390/curroncol28030182.
3
Inflammatory breast cancer associated with amyopathic dermatomyositis: a case report.与无肌病性皮肌炎相关的炎性乳腺癌:一例报告
Surg Case Rep. 2020 Nov 11;6(1):284. doi: 10.1186/s40792-020-01066-7.
4
Dermatomyositis: A Presenting Clinical Vignette in a Patient With Breast Cancer.皮肌炎:一例乳腺癌患者的首发临床病例
Cureus. 2020 Sep 23;12(9):e10624. doi: 10.7759/cureus.10624.
5
Paraneoplastic dermatomyositis in hereditary breast and ovarian cancer syndrome.
Breast J. 2020 Sep;26(9):1836-1837. doi: 10.1111/tbj.13888. Epub 2020 May 18.
6
Clinico-Immunological Profile of a 67-Year-Old Woman Affected by HER2-Positive Breast Cancer and Autoimmune Dermatomyositis.一名67岁HER2阳性乳腺癌合并自身免疫性皮肌炎女性的临床免疫学特征
Front Oncol. 2020 Feb 25;10:192. doi: 10.3389/fonc.2020.00192. eCollection 2020.
7
Dermatomyositis and malignancy.皮肌炎与恶性肿瘤
Can Fam Physician. 2019 Jun;65(6):409-411.
8
Breast Cancer with Paraneoplastic Syndrome in a 72 Year Old Male Patient.一名72岁男性患者的伴副肿瘤综合征的乳腺癌
Mymensingh Med J. 2019 Jan;28(1):254-258.
9
Breast cancer with dermatomyositis as initial presentation.以皮肌炎为首发表现的乳腺癌。
Med J Malaysia. 2018 Feb;73(1):44-45.
10
[A Case of Breast Cancer Associated with Dermatitis That Was Difficult to Differentiate from Dermatomyositis].
Gan To Kagaku Ryoho. 2017 Nov;44(12):1930-1932.

根治性乳腺癌手术后症状性皮肌炎显著缓解。

Remarkable remission of symptomatic dermatomyositis after curative breast cancer surgery.

作者信息

Fujino Makoto, Kawashima Masahiro, Yoshifuji Hajime, Nakashima Ran, Yamada Yosuke, Matsumoto Yoshiaki, Kawaguchi-Sakita Nobuko, Mori Yukiko, Pu Fengling, Yamaguchi Ayane, Kawaguchi Kosuke, Takada Masahiro, Toi Masakazu

机构信息

Department of Breast Surgery, Kyoto University Hospital, 54 Shogoin-Kawahara-cho, Sakyo-ku, Kyoto, 6068507 Japan.

Department of Breast Surgery, Uji Tokushukai Hospital, 145 Ishibashi, Makishima-cho, Uji City, Kyoto 6110041 Japan.

出版信息

Int Cancer Conf J. 2024 Jan 25;13(2):111-118. doi: 10.1007/s13691-023-00646-2. eCollection 2024 Apr.

DOI:10.1007/s13691-023-00646-2
PMID:38524641
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10957833/
Abstract

Dermatomyositis (DM) is an autoimmune disease that causes proximal muscle weakness in the extremities leading to severe immobility and dysphagia. Approximately 20% of patients with DM are positive for anti-TIF-1γ antibody and frequently accompanied by malignant tumors. Although DM remission after tumor resection has been reported, the indications for surgery in patients with severe DM are unknown. Herein, we report a case of a 79-year-old Japanese woman who presented with breast cancer and anti-TIF-1γ antibody-positive DM. She became bedridden shortly after DM onset. Although pulsed steroid therapy, intravenous immunoglobulin, tacrolimus, and endocrine therapy with fulvestrant did not improve her symptoms, tumor resection with axillary lymph node dissection resulted in complete remission of the DM after 8 months. Immunohistochemistry revealed high expression of TIF-1γ in cancer cells, both in the primary tumor and axillary lymph nodes. Since the serum levels of anti-TIF-1γ antibody decreased after the surgery, the existence of breast cancer with TIF-1γ expression may have contributed to the worsening of DM. The present case suggests that curative surgery should be considered as a treatment option even if the patient has severe symptoms, such as immobility and dysphagia. Careful discussions with patients and multidisciplinary collaboration are essential to make surgery feasible, particularly for those with severe symptomatic DM.

摘要

皮肌炎(DM)是一种自身免疫性疾病,可导致四肢近端肌肉无力,进而引起严重的活动障碍和吞咽困难。约20%的DM患者抗TIF-1γ抗体呈阳性,且常伴有恶性肿瘤。尽管已有肿瘤切除后DM缓解的报道,但严重DM患者的手术指征尚不清楚。在此,我们报告一例79岁日本女性患者,她患有乳腺癌且抗TIF-1γ抗体阳性的DM。DM发病后不久她就卧床不起。尽管脉冲类固醇疗法、静脉注射免疫球蛋白、他克莫司以及氟维司群内分泌治疗均未能改善她的症状,但行腋窝淋巴结清扫的肿瘤切除术8个月后DM完全缓解。免疫组化显示,原发肿瘤和腋窝淋巴结的癌细胞中TIF-1γ均高表达。由于术后抗TIF-1γ抗体血清水平下降,表达TIF-1γ的乳腺癌可能促使了DM病情恶化。本病例提示,即使患者有严重症状,如活动障碍和吞咽困难,也应考虑将根治性手术作为一种治疗选择。与患者进行仔细讨论并开展多学科协作对于使手术可行至关重要,尤其是对于那些有严重症状性DM的患者。