库欣病表现为复发性脓肿,缓解后出现甲状腺功能亢进。

IF 0.7 Q4 ENDOCRINOLOGY & METABOLISM Endocrinology, Diabetes and Metabolism Case Reports Pub Date : 2024-05-31 Print Date: 2024-04-01 DOI:10.1530/EDM-23-0040
Ewa Stogowska, Agnieszka Łebkowska, Maria Kościuszko, Grzegorz Zieliński, Irina Kowalska, Monika Karczewska-Kupczewska
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引用次数: 0

摘要

摘要:我们报告了一例患有库欣病的 59 岁女性患者,她在接受高皮质醇血症治疗后出现了甲状腺功能亢进。患者曾因多处软组织脓肿反复住院,入院时已出现败血症。病史和体格检查均提示她患有库欣综合征。脓毒症治疗后进行的最初激素诊断过程得出了相互矛盾的结果。然而,3 个月后再次进行的激素评估显示患者患有垂体高皮质血症,通过双侧下蝶窦取样证实了这一情况,并通过经蝶垂体手术成功治疗。术后三个月,患者因甲状腺功能亢进症状再次入院,经实验室检查证实为甲状腺功能亢进。甲状腺闪烁扫描显示患者患有巴塞杜氏病。然而,患者体内没有抗促甲状腺激素抗体,这表明甲亢还有其他病因。最终,患者接受了放射性碘治疗。目前,她的病情正在好转,没有再出现脓肿、严重感染或甲亢。总之,虽然高皮质醇血症的临床表现可能是非特异性的,但其治疗可能会引发自身免疫性疾病:学习要点:反复出现严重感染应促使医生考虑高皮质醇血症的可能性。慢性高皮质醇血症会使人衰弱,并可能导致严重残疾。对患有活动性或近期严重炎症或感染性疾病的患者进行地塞米松抑制试验,可能会产生误导或混淆的结果。临床医生应注意,在成功治疗高皮质醇血症后,可能会出现自身免疫性疾病。
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Cushing's disease presenting with recurrent abscesses followed by post-remission hyperthyroidism.

Summary: We report a case of a 59-year-old woman with Cushing's disease who developed hyperthyroidism following treatment of hypercortisolaemia. The patient with a history of recurrent hospitalisations caused by multi-sited soft tissue abscesses was admitted with sepsis. Both her medical history and physical examination suggested Cushing's syndrome. The initial hormonal diagnostic process, conducted after sepsis treatment, brought forth conflicting results. However, hormonal assessment repeated 3 months later indicated pituitary hypercortisolaemia, which was confirmed through bilateral inferior petrosal sinus sampling and was successfully treated with transsphenoidal pituitary surgery. Three months after the surgery, the patient was readmitted to our epartment with symptoms of hyperthyroidism, which was confirmed by laboratory tests. Thyroid scintiscans indicated Graves' disease. However, the absence of anti-thyroid stimulating hormone antibodies suggested other etiologies of hyperthyroidism. Eventually, the patient underwent radioiodine therapy. Currently, her condition is improving and she has had no recurrence of abscesses, severe infections, or hyperthyroidism. In conclusion, while clinical manifestation of hypercortisolaemia might be non-specific, its treatment may trigger the development of autoimmune diseases.

Learning points: The presence of recurrent severe infections should prompt physicians to consider the possibility of hypercortisolaemia. Chronic hypercortisolism is debilitating and can lead to significant disability. Dexamethasone suppression testing in patients with active or recent severe inflammatory or infectious illnesses may produce misleading or confusing results. Clinicians should be aware of the potential development of autoimmune diseases following successful treatment of hypercortisolaemia.

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来源期刊
CiteScore
1.50
自引率
0.00%
发文量
142
审稿时长
9 weeks
期刊介绍: Endocrinology, Diabetes & Metabolism Case Reports publishes case reports on common and rare conditions in all areas of clinical endocrinology, diabetes and metabolism. Articles should include clear learning points which readers can use to inform medical education or clinical practice. The types of cases of interest to Endocrinology, Diabetes & Metabolism Case Reports include: -Insight into disease pathogenesis or mechanism of therapy - Novel diagnostic procedure - Novel treatment - Unique/unexpected symptoms or presentations of a disease - New disease or syndrome: presentations/diagnosis/management - Unusual effects of medical treatment - Error in diagnosis/pitfalls and caveats
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