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泊沙康唑致慢性粒单核细胞白血病患者肾上腺功能不全一例

Posaconazole-Induced Adrenal Insufficiency in a Case of Chronic Myelomonocytic Leukemia.

作者信息

Miller Ann, Brooks Lauren K, Poola-Kella Silpa, Malek Rana

机构信息

Department of Medicine, University of Maryland Medical Center, Baltimore, MD, USA.

Department of Medicine, Division of Endocrinology, Diabetes and Nutrition, University of Maryland Medical Center, Baltimore, MD, USA.

出版信息

Case Rep Endocrinol. 2018 Jan 16;2018:2170484. doi: 10.1155/2018/2170484. eCollection 2018.

Abstract

INTRODUCTION

Posaconazole is an azole used in treatment and prophylaxis of a broad spectrum of fungal infections. Antifungals such as ketoconazole have been shown to cause primary adrenal insufficiency (AI) as a result of direct inhibition on the steroidogenesis pathway. There is only one reported case of primary AI induced by posaconazole in a patient with mucormycosis. We report a case of posaconazole-related primary AI.

CASE

A 63-year-old man with chronic myelomonocytic leukemia was admitted for fatigue and intermittent nausea and vomiting. He had recently discontinued prophylactic posaconazole 300 mg daily. He was assessed for AI with a morning cortisol of 1.9 mcg/dL followed by a failed cosyntropin stimulation (CS) test. Adrenocorticotropic hormone (ACTH) level was 154.6 pg/mL with negative 21-hydroxylase antibodies. The patient's symptoms improved with initiation of hydrocortisone and fludrocortisone. One year after discontinuation of posaconazole, he underwent a repeat CS test which showed normal adrenal function with normal ACTH at 34.1 pg/mL.

CONCLUSION

In this case, we demonstrate that prolonged use of posaconazole is associated with primary AI. As use of posaconazole increases, knowledge of the potential risk of AI is important and must be included in the differential diagnosis when these patients present with hypotension, hypoglycemia, and failure to thrive.

摘要

引言

泊沙康唑是一种用于治疗和预防多种真菌感染的唑类药物。酮康唑等抗真菌药物已被证明可因直接抑制类固醇生成途径而导致原发性肾上腺皮质功能减退(AI)。仅有一例报告显示患有毛霉菌病的患者因泊沙康唑诱发原发性AI。我们报告一例与泊沙康唑相关的原发性AI病例。

病例

一名63岁慢性粒单核细胞白血病男性因疲劳及间歇性恶心呕吐入院。他最近停用了每日300毫克的预防性泊沙康唑。对其进行AI评估时,晨间皮质醇水平为1.9微克/分升,随后促肾上腺皮质激素(ACTH)刺激试验(CS)结果不佳。促肾上腺皮质激素(ACTH)水平为154.6皮克/毫升,21-羟化酶抗体阴性。患者在开始使用氢化可的松和氟氢可的松后症状改善。停用泊沙康唑一年后,他接受了重复CS试验,结果显示肾上腺功能正常,ACTH正常,为34.1皮克/毫升。

结论

在本病例中,我们证明长期使用泊沙康唑与原发性AI有关。随着泊沙康唑使用的增加,了解AI的潜在风险很重要,当这些患者出现低血压、低血糖和发育不良时,必须将其纳入鉴别诊断。

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