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抗凝及慢性免疫性血小板减少症导致双侧肾上腺出血后出现肾上腺皮质功能不全。

Adrenocortical insufficiency after bilateral adrenal hemorrhage due to anticoagulation and chronic immunothrombocytopenia.

作者信息

Hintze Sophie Charlotte, Beuschlein Felix

机构信息

Department of Endocrinology, Diabetology and Clinical Nutrition, University Hospital Zurich, Zurich, Switzerland.

出版信息

Endocrinol Diabetes Metab Case Rep. 2024 Nov 20;2024(4). doi: 10.1530/EDM-24-0034. Print 2024 Oct 1.

Abstract

SUMMARY

Adrenocortical insufficiency is defined as the clinical manifestation of chronic glucocorticoid and/or mineralocorticoid deficiency due to failure of the adrenal cortex. It may result in an adrenal crisis, which is a life-threatening disease; thus, prompt initiation of therapy with hydrocortisone is necessary. Symptoms such as hypotension, weight loss, or fatigue are not specific, which is why diagnosis is delayed in many cases. Our patient suffered from immune thrombocytopenia (ITP), an acquired thrombocytopenia caused by an autoimmune reaction against platelets and megakaryocytes. Primary ITP, in which no triggering cause can be identified, must be distinguished from secondary forms (e.g. in the context of systemic autoimmune diseases, lymphomas, or (rarely) by drugs). Patients may be asymptomatic at presentation or may present with a range of mild mucocutaneous to life-threatening bleeding. Here, we report on a 43-year-old woman who had developed adrenocortical insufficiency due to bilateral hemorrhage in the adrenal glands. Because of anticoagulation with phenprocoumon after pulmonary embolism and thrombocytopenia on the basis of ITP, the patient had an increased risk of bleeding. Due to the nonspecific and ambiguous symptoms of adrenocortical insufficiency, prompt diagnosis remains a challenge.

LEARNING POINTS

Hypocortisolism or adrenal crisis with nonspecific symptoms, especially abdominal and gastrointestinal, is often misinterpreted. Diagnosis of adrenal insufficiency is often delayed because of the initial ambiguous presentation; physicians must be aware to avoid adrenal crisis. Especially in patients with several risk factors for bleeding, unusual bleeding manifestations, such as adrenal hemorrhage, must be considered. Immediate treatment is necessary by substituting hydrocortisone in a higher dosage, and in most cases, fludrocortisone. During the course of treatment, the amount of hydrocortisone can be reduced to a substitution dosage (15-25 mg/day divided into two to three doses/day). Fludrocortisone should be continued at a dosage of 0.05-0.1 mg/day, depending on blood pressure and sodium and potassium levels. All patients should carry a medical alert notification or a steroid emergency card. In the case of trauma, surgery, or other stressful events, hydrocortisone must be administered in higher dosages (e.g. 100 mg i.v.).

摘要

摘要

肾上腺皮质功能不全被定义为由于肾上腺皮质功能衰竭导致慢性糖皮质激素和/或盐皮质激素缺乏的临床表现。它可能会引发肾上腺危象,这是一种危及生命的疾病;因此,必须立即开始用氢化可的松进行治疗。低血压、体重减轻或疲劳等症状并不具有特异性,这就是为什么在许多情况下诊断会延迟。我们的患者患有免疫性血小板减少症(ITP),这是一种由针对血小板和巨核细胞的自身免疫反应引起的获得性血小板减少症。必须将无法确定触发原因的原发性ITP与继发性形式(例如在系统性自身免疫性疾病、淋巴瘤或(罕见)药物的背景下)区分开来。患者在就诊时可能无症状,也可能表现出一系列从轻度黏膜皮肤出血到危及生命的出血症状。在此,我们报告一名43岁女性,她因双侧肾上腺出血而出现肾上腺皮质功能不全。由于肺栓塞后使用苯丙香豆素抗凝以及基于ITP的血小板减少症,该患者出血风险增加。由于肾上腺皮质功能不全的症状不具有特异性且模糊不清,及时诊断仍然是一项挑战。

学习要点

低皮质醇血症或肾上腺危象伴有非特异性症状,尤其是腹部和胃肠道症状,常常被误解。由于最初表现不明确,肾上腺功能不全的诊断常常延迟;医生必须意识到要避免肾上腺危象。特别是在有多种出血危险因素的患者中,必须考虑不寻常的出血表现,如肾上腺出血。必须立即用更高剂量的氢化可的松进行治疗,在大多数情况下还需使用氟氢可的松。在治疗过程中,氢化可的松的剂量可减至替代剂量(每天15 - 25毫克,分为每日两到三次给药)。氟氢可的松应根据血压以及钠和钾水平,以每天0.05 - 0.1毫克的剂量持续使用。所有患者都应携带医疗警示通知或类固醇急救卡。在发生创伤、手术或其他应激事件时,必须给予更高剂量的氢化可的松(例如静脉注射100毫克)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02ef/11623252/14e9ef0672cf/EDM24-0034fig1.jpg

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