Kondle Shreya, Cohen Stanley
Internal Medicine, Texas Health Presbyterian Hospital of Dallas, Dallas, USA.
Internal Medicine, The University of Texas Southwestern Medical School, Dallas, USA.
Cureus. 2025 Feb 17;17(2):e79178. doi: 10.7759/cureus.79178. eCollection 2025 Feb.
Dermatomyositis (DM) is an immune-mediated inflammatory myopathy that can present with proximal muscle weakness and characteristic skin findings. Nuclear matrix protein 2 (NXP-2)-positive DM, while rare, has a strong association with malignancy. It can display features such as muscle weakness, subcutaneous edema, and refractory dysphagia, all of which were present in our 63-year-old male patient. He experienced a prolonged hospitalization and percutaneous endoscopic gastrostomy (PEG) tube placement. He improved with prednisone, azathioprine, rituximab, and intravenous immunoglobulin (IVIG) treatments. For over two years, he has had no evidence of malignancy. This case underscores the complexity of NXP-2-positive DM and the potential for severe presentations that may require the usage of second-line therapies.
皮肌炎(DM)是一种免疫介导的炎症性肌病,可表现为近端肌无力和特征性皮肤表现。核基质蛋白2(NXP-2)阳性的皮肌炎虽然罕见,但与恶性肿瘤密切相关。它可表现出肌无力、皮下水肿和难治性吞咽困难等特征,我们这位63岁的男性患者就出现了所有这些症状。他经历了长时间住院并接受了经皮内镜下胃造口术(PEG)置管。他在接受泼尼松、硫唑嘌呤、利妥昔单抗和静脉注射免疫球蛋白(IVIG)治疗后病情有所改善。两年多来,他没有恶性肿瘤的迹象。该病例突显了NXP-2阳性皮肌炎的复杂性以及可能需要使用二线治疗的严重临床表现的可能性。