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Malignant atrophic papulosis with motor aphasia and intestinal perforation: A case report and review of published works

机译:恶性萎缩性丘疹病伴运动性失语和肠穿孔:病例报告和已发表著作的综述

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摘要

Malignant atrophic papulosis (MAP) is a rare type of obliterating vasculopathy that can present as pure cutaneous lesions or a systemic entity affecting multiple organs. Systemic disease, such as gastrointestinal or central nervous system involvement, may predispose the patients to poorer or even fatal outcomes. We present a 30‐year‐old female patient with systemic manifestation of MAP 10 days after delivery of a full‐term pregnancy who subsequently developed motor aphasia and intestinal perforation. The patient was administrated empirical treatment with an antiplatelet, anticoagulant, methylprednisolone sodium succinate and alprostadil. Antibiotics were administrated due to intestinal perforation and secondary sepsis. Despite all treatment, the patient died a week later. We summarized all the previous reports of MAP based on thorough review of previous published work. Overall, this is the first patient with MAP combined with motor aphasia and intestinal perforation and may provide insights for future studies on the treatment of this disease.
机译:恶性萎缩性丘疹病(MAP)是一种罕见的闭塞性血管病,可表现为单纯的皮肤病变或影响多个器官的全身性实体。系统性疾病,例如胃肠道或中枢神经系统受累,可能使患者更容易出现甚至致命的后果。我们介绍了一名30岁的女性患者,该患者在足月妊娠分娩10天后出现全身性MAP,随后出现运动性失语和肠穿孔。使用抗血小板,抗凝剂,甲基泼尼松龙琥珀酸钠和前列地尔对患者进行经验性治疗。由于肠穿孔和继发性败血症而使用了抗生素。尽管进行了所有治疗,该患者在一周后死亡。我们在全面回顾了先前发表的工作的基础上,总结了MAP的所有先前报告。总体而言,这是首例MAP合并运动性失语和肠穿孔的MAP患者,可能为该疾病的治疗研究提供参考。

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