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[MEP - 46] 一例环孢素相关的早期色素沉着病例。

[MEP-46] A Case of Cyclosporine-Associated Early Hyperpigmentation.

作者信息

Güler Ali Umut, Coşkun Yücel Nazlı Melis, Sabuncu Timuçin, Güvener Murat

机构信息

Department of Cardiovascular Surgery, Hacettepe University Faculty of Medicine, Ankara, Türkiye.

出版信息

Turk Gogus Kalp Damar Cerrahisi Derg. 2024 Dec 31;32(4 Suppl 2):144-145. doi: 10.5606/tgkdc.dergisi.2024.mep-46. eCollection 2024 Nov.

Abstract

Cyclosporine is an immunosuppressive agent used to prevent rejection in organ transplants, as well as for the treatment of various immune diseases involving dermatological, hematological, renal, gastroenterological, neurological, and musculoskeletal systems. Cyclosporine has side effects such as blurred vision, fatigue, stomach discomfort, nephrotoxicity, hepatotoxicity, infections, lymphoma, hypertrichosis, gingivitis, and central nervous system toxicity. Herein, we presented a case of heart transplantation where a rare side effect of cyclosporine, hyperpigmentation, was observed. A 46-year-old female patient underwent heart transplantation surgery. Prednisone, mycophenolate mofetil, and tacrolimus were initiated as immunosuppressive therapy. Due to the involvement of tacrolimus in the etiology of posterior reversible encephalopathy syndrome, cyclosporine was chosen as the immunosuppressant. The patient was started on 300 mg of cyclosporine once daily (5 mg/kg/day), and the dosage was adjusted based on daily blood levels. Six days after starting cyclosporine therapy, widespread hyperpigmentation and hirsutism were noticed on the patient's body. Etiological factors such as adrenal insufficiency, drug therapy, and hemochromatosis, which could cause generalized hyperpigmentation, were ruled out. The existing hyperpigmentation was associated with cyclosporine therapy. Cyclosporine is a calcineurin inhibitor. According to the literature, cyclosporine-associated hyperpigmentation, hirsutism, hypertrichosis, and darkening of hair color are rare side effects. These have been observed with both oral and topical use. However, the literature shows that the onset of these side effects typically occurs between 45 days and four months after the initiation of the drug. In our experience, despite the patient not receiving a high dose of cyclosporine, the side effects emerged within six days, and no cases of such early occurrence have been reported in the literature.

摘要

环孢素是一种免疫抑制剂,用于预防器官移植中的排斥反应,以及治疗涉及皮肤、血液、肾脏、胃肠、神经和肌肉骨骼系统的各种免疫疾病。环孢素有副作用,如视力模糊、疲劳、胃部不适、肾毒性、肝毒性、感染、淋巴瘤、多毛症、牙龈炎和中枢神经系统毒性。在此,我们报告了一例心脏移植病例,观察到环孢素一种罕见的副作用——色素沉着。一名46岁女性患者接受了心脏移植手术。开始使用泼尼松、霉酚酸酯和他克莫司作为免疫抑制治疗。由于他克莫司与后部可逆性脑病综合征的病因有关,选择环孢素作为免疫抑制剂。患者开始每天服用300毫克环孢素(5毫克/千克/天),并根据每日血药浓度调整剂量。开始环孢素治疗六天后,患者身体上出现了广泛的色素沉着和多毛症。排除了可能导致全身性色素沉着的病因,如肾上腺功能不全、药物治疗和血色素沉着症。现有的色素沉着与环孢素治疗有关。环孢素是一种钙调神经磷酸酶抑制剂。根据文献,环孢素相关的色素沉着、多毛症、毛发增多和头发颜色变黑是罕见的副作用。口服和外用均有观察到这些情况。然而,文献表明,这些副作用通常在药物开始使用后的45天至四个月之间出现。根据我们的经验,尽管患者没有接受高剂量的环孢素,但副作用在六天内就出现了,文献中尚未报道过如此早出现的病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3669/12045216/6895d45840a0/TJTCS-2024-11-100-144-145-F1.jpg

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