继发于弥漫性特发性神经内分泌细胞增生症的异位库欣综合征--2 个病例的报告。

JCEM case reports Pub Date : 2024-08-06 eCollection Date: 2024-08-01 DOI:10.1210/jcemcr/luae128
Raul Lopez Fanas, Travis Goettemoeller, Keerthi Cedeno, Anjali D Manavalan
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引用次数: 0

摘要

异位促肾上腺皮质激素分泌(EAS)占库欣综合征病例总数的 10%至 20%。弥漫性肺内神经内分泌细胞增生症(DIPNECH)是一种鲜为人知的肺部疾病,其特点是支气管粘膜神经内分泌细胞异常增生。它被认为是肺类癌的前兆,在少数病例中与 EAS 有关。我们报告了两名具有 DIPNECH 临床、放射学和病理学特征的患者,他们继发于 EAS,表现为症状发作迅速、血浆促肾上腺皮质激素和皮质醇水平升高,以及大剂量地塞米松抑制试验失败。高皮质醇症的治疗包括切除受累肺部和使用类固醇生成抑制剂。尽管最初采取了积极的治疗措施,但高皮质醇症仍持续存在。这组病例强调了在适当的临床情况下将 DIPNECH 作为库欣综合征病因的重要性,并强调了由于这种疾病的弥漫性,手术可能无法治愈。鉴于 EAS 的死亡率很高,当初始手术失败时,及时的药物治疗、适当的预防措施和双侧肾上腺切除术可能是挽救生命的措施。
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Ectopic Cushing Syndrome Secondary to Diffuse Idiopathic Neuroendocrine Cell Hyperplasia-A Report of 2 Cases.

Ectopic ACTH secretion (EAS) accounts for 10% to 20% of all Cushing syndrome cases. Diffuse intrapulmonary neuroendocrine cell hyperplasia (DIPNECH), a poorly understood lung disease, is characterized by abnormal proliferation of neuroendocrine cells in the bronchial mucosa. It is thought to be a precursor of pulmonary carcinoid and has been associated with EAS in a handful of cases. We present 2 patients with clinical, radiological, and pathological features of DIPNECH who presented with florid Cushing syndrome secondary to EAS evidenced by rapid onset of symptoms, elevated plasma ACTH, and cortisol levels, and failed high-dose dexamethasone suppression testing. Treatment of hypercortisolism included excision of the involved lung and medical therapy with steroidogenesis inhibitors. Despite the aggressive initial management, hypercortisolism persisted. This case series highlights the importance of considering DIPNECH as a cause for Cushing syndrome in the appropriate clinical scenario and underscores the likelihood that surgery may not be curative because of the diffuse nature of this disease. Given the high mortality associated with EAS, prompt medical therapy, appropriate prophylaxis, and bilateral adrenalectomy can be lifesaving measures when initial surgery fails.

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