Pericardial artery lymphoma in a patient with dermatomyositis: A case report.

IF 0.9 Q4 RHEUMATOLOGY
Kei Hirose, Takayuki Katsuyama, Natsuki Kubota, Yuya Terajima, Kazuya Matsumoto, Kenta Shidahara, Takato Nakadoi, Shoichi Nawachi, Yu Katayama, Yoshia Miyawaki, Eri Katsuyama, Mariko Narazaki-Takano, Yoshinori Matsumoto, Noboru Asada, Ken-Ei Sada, Jun Wada
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引用次数: 0

Abstract

A woman in her 60s presented with erythema on both elbows, dyspnea on exertion, discomfort, and swelling of the left upper extremity, followed by swelling and myalgia of the right upper and lower extremities. She was diagnosed with anti-TIF1γ antibody-positive dermatomyositis with interstitial pneumonia. The initial screening tests for malignant diseases including contrast-enhanced CT, upper and lower endoscopy, and gynecological examination did not reveal any obvious abnormalities. The patient experienced two recurrent episodes of muscle weakness and dysphagia during treatment with intravenous glucocorticoids and cyclophosphamide. Five months after diagnosis, a bone marrow biopsy and positron emission tomography- computed tomography (PET-CT) scan revealed a coronary malignant lymphoma with suspected systemic metastasis. Although chemotherapy was initiated, the patient ultimately succumbed to alveolar hemorrhage. Coronary lymphoma is very rare and there has been no report of a cases associated with myositis. PET-CT may be useful for searching malignancy in anti-TIF1γ antibody-positive dermatomyositis cases of recurrent relapse.

皮肌炎患者的心包动脉淋巴瘤:病例报告。
一名 60 多岁的妇女出现双肘红斑、用力时呼吸困难、不适以及左上肢肿胀,随后右上下肢肿胀和肌痛。她被诊断为抗 TIF1γ 抗体阳性皮肌炎伴间质性肺炎。最初的恶性疾病筛查包括对比增强 CT、上下内窥镜检查和妇科检查,均未发现明显异常。在静脉注射糖皮质激素和环磷酰胺治疗期间,患者反复出现两次肌无力和吞咽困难。确诊五个月后,骨髓活检和正电子发射计算机断层扫描(PET-CT)发现了冠状恶性淋巴瘤,并怀疑有全身转移。虽然进行了化疗,但患者最终还是死于肺泡出血。冠状淋巴瘤非常罕见,目前还没有与肌炎相关的病例报道。正电子发射计算机断层扫描(PET-CT)可用于搜索抗TIF1γ抗体阳性皮肌炎复发病例中的恶性肿瘤。
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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CiteScore
1.40
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