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冻伤和冷凝集素病:两种实体共存导致不良临床结局。

Frostbite and Cold Agglutinin Disease: Coexistence of Two Entities Leading to Poor Clinical Outcomes.

机构信息

Service de Médecine Interne, Diabète et Maladies Métaboliques, Hôpitaux Universitaires de Strasbourg, 67000 Strasbourg, France.

Service des Urgences, Hôpitaux Universitaires de Strasbourg, 67000 Strasbourg, France.

出版信息

Medicina (Kaunas). 2021 Jun 8;57(6):592. doi: 10.3390/medicina57060592.

DOI:10.3390/medicina57060592
PMID:34201186
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8230137/
Abstract

An 83-year-old woman was admitted to the emergency department for a 7-day history of fatigue and progressive cyanosis in the feet and hands after cold exposure despite physical protective measures. Upon arrival, the patient presented with necrotic cutaneous lesions in both hands and distal lower extremities. Upon admission, hemoglobin was 7.6 g/dL and laboratory tests were consistent with cold agglutinin disease (CAD), the presence of monoclonal IgM, and flow cytometry consistent with lymphoplasmacytic lymphoma, but MYD88 L265P mutation was negative. The patient required blood transfusion, resulting in stabilized hemoglobin and a decrease in markers of hemolysis. Treatment with aspirin 250 mg daily and intravenous iloprost 0.5 mL/h was initiated with a poor clinical response at day 4. Amputation was required. Plasma exchange was performed and chemotherapy with rituximab and bendamustine was initiated. The clinical course was marked by further necrosis, prompting discussions regarding an additional amputation that was not performed considering the high surgical risk and refusal by the patient. Supportive treatment was initiated, and the patient expired one month after hospital admission.

摘要

一位 83 岁女性,因在寒冷暴露后出现 7 天疲劳和手足进行性发绀而入住急诊部,尽管采取了身体保护措施。入院时,患者双手和下肢远端均出现坏死性皮肤病变。入院时血红蛋白为 7.6g/dL,实验室检查符合冷凝集素病(CAD),存在单克隆 IgM,流式细胞术符合淋巴浆细胞淋巴瘤,但 MYD88 L265P 突变阴性。患者需要输血,血红蛋白稳定,溶血标志物下降。给予每日 250mg 阿司匹林和 0.5ml/h 静脉内伊洛前列素治疗,但第 4 天临床反应不佳。需要截肢。进行了血浆置换,并开始用利妥昔单抗和苯达莫司汀进行化疗。临床过程中出现进一步的坏死,促使讨论是否进行额外的截肢,但由于手术风险高和患者拒绝,未进行截肢。开始了支持性治疗,患者在入院后一个月死亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a26d/8230137/a1e42eb9e698/medicina-57-00592-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a26d/8230137/35792919efca/medicina-57-00592-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a26d/8230137/a1e42eb9e698/medicina-57-00592-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a26d/8230137/35792919efca/medicina-57-00592-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a26d/8230137/a1e42eb9e698/medicina-57-00592-g002.jpg

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Int J Circumpolar Health. 2023 Dec;82(1):2189552. doi: 10.1080/22423982.2023.2189552.

本文引用的文献

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Frostbite: Pathophysiology, Epidemiology, Diagnosis, Treatment, and Prevention.冻伤:病理生理学、流行病学、诊断、治疗及预防
J Spec Oper Med. 2020 Winter;20(4):123-135. doi: 10.55460/PDX9-BG8G.
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Cold agglutinin disease: current challenges and future prospects.冷凝集素病:当前挑战与未来展望
J Blood Med. 2019 Apr 9;10:93-103. doi: 10.2147/JBM.S177621. eCollection 2019.
3
How I manage patients with cold agglutinin disease.冷抗体自身免疫性溶血性贫血的诊治策略
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Cold agglutinin disease presenting as livedo racemosa.以网状青斑为表现的冷凝集素病。
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Blood. 2017 Jul 27;130(4):537-541. doi: 10.1182/blood-2017-04-778175. Epub 2017 May 22.
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Primary cold agglutinin-associated lymphoproliferative disease: a B-cell lymphoma of the bone marrow distinct from lymphoplasmacytic lymphoma.原发性冷凝集素相关淋巴增殖性疾病:一种与淋巴浆细胞淋巴瘤不同的骨髓B细胞淋巴瘤。
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7
Cold agglutinin-mediated autoimmune hemolytic anemia in Waldenström's macroglobulinemia.华氏巨球蛋白血症中冷凝集素介导的自身免疫性溶血性贫血。
Clin Lymphoma Myeloma. 2009 Mar;9(1):110-2. doi: 10.3816/CLM.2009.n.030.
8
Primary chronic cold agglutinin disease: a population based clinical study of 86 patients.原发性慢性冷凝集素病:一项基于86例患者的人群临床研究。
Haematologica. 2006 Apr;91(4):460-6.