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本文引用的文献

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Primary bilateral macronodular adrenal hyperplasia: definitely a genetic disease.双侧原发性巨结节性肾上腺增生:明确的遗传性疾病。
Nat Rev Endocrinol. 2022 Nov;18(11):699-711. doi: 10.1038/s41574-022-00718-y. Epub 2022 Aug 3.
2
How to rule out non-neoplastic hypercortisolemia (previously known as pseudo-cushing).如何排除非肿瘤性皮质醇增多症(以前称为假性库欣综合征)。
Pituitary. 2022 Oct;25(5):701-704. doi: 10.1007/s11102-022-01222-2. Epub 2022 May 26.
3
Primary Hepatic Neuroendocrine Tumor With Ectopic Adrenocorticotropic Hormone Production.原发性肝神经内分泌肿瘤伴异位促肾上腺皮质激素分泌
Cureus. 2022 Mar 2;14(3):e22771. doi: 10.7759/cureus.22771. eCollection 2022 Mar.
4
Paraneoplastic Cushing Syndrome in Gastrointestinal Neuroendocrine Tumour.胃肠道神经内分泌肿瘤伴发的副肿瘤性库欣综合征
Case Rep Oncol. 2021 Sep 23;14(3):1407-1413. doi: 10.1159/000518316. eCollection 2021 Sep-Dec.
5
Pitfalls in Performing and Interpreting Inferior Petrosal Sinus Sampling: Personal Experience and Literature Review.岩下窦取样操作与解读中的陷阱:个人经验及文献综述
J Clin Endocrinol Metab. 2021 Apr 23;106(5):e1953-e1967. doi: 10.1210/clinem/dgab012.
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The 2019 WHO classification of tumours of the digestive system.2019年世界卫生组织消化系统肿瘤分类。
Histopathology. 2020 Jan;76(2):182-188. doi: 10.1111/his.13975. Epub 2019 Nov 13.
7
Clinicopathological correlates of adrenal Cushing's syndrome.肾上腺库欣综合征的临床病理相关性
J Clin Pathol. 2015 Mar;68(3):175-86. doi: 10.1136/jclinpath-2014-202612. Epub 2014 Nov 25.
8
Gastroenteropancreatic high-grade neuroendocrine carcinoma.胃肠胰高分化神经内分泌癌
Cancer. 2014 Sep 15;120(18):2814-23. doi: 10.1002/cncr.28721. Epub 2014 Apr 25.
9
Neuroendocrine tumor in liver with positive ACTH receptor: a case report.肝脏中具有促肾上腺皮质激素(ACTH)受体阳性的神经内分泌肿瘤:一例报告
J Pediatr Hematol Oncol. 2014 Jan;36(1):e1-4. doi: 10.1097/MPH.0b013e318286d2ba.
10
Primary hepatic carcinoid tumor presenting as Cushing's syndrome.以库欣综合征为表现的原发性肝类癌肿瘤。
J Endocrinol Invest. 2007 Apr;30(4):327-33. doi: 10.1007/BF03346308.

伴有库欣综合征的肝脏促肾上腺皮质激素分泌性神经内分泌癌

ACTH-Producing Neuroendocrine Carcinoma of the Liver with Cushing's Syndrome.

作者信息

Sandozi Mudassar, Pamulapati Saagar, Zaidi Aniqa, Stuart Zuzanna, Pamulapati Sneha, Doniparthi Ajay

机构信息

Javon Bea Hospital-Rockton, Rockford, IL, USA.

Midwestern University, Downers Grove, IL, USA.

出版信息

Case Rep Oncol Med. 2023 Sep 26;2023:9946271. doi: 10.1155/2023/9946271. eCollection 2023.

DOI:10.1155/2023/9946271
PMID:37794851
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10547567/
Abstract

Paraneoplastic Cushing's syndrome arises when neuroendocrine tumors cause excess glucocorticoid production. We report a case of ectopic ACTH-producing liver neuroendocrine tumor. A 71 y.o. female with a history of rectal squamous carcinoma presented with fatigue and diffuse swelling. Liver biopsy revealed metastatic neuroendocrine carcinoma. Workup revealed markedly elevated morning cortisol and ACTH. Overnight dexamethasone suppression testing and positive immunostaining for ACTH on biopsy suggested paraneoplastic Cushing's syndrome secondary to neuroendocrine hepatic tumors with bony metastasis. This explained the patient's persistent anasarca, hyperglycemia, and electrolyte abnormalities. Despite multiple interventions, the patient's clinical status declined, and she expired.

摘要

副肿瘤性库欣综合征是由神经内分泌肿瘤导致糖皮质激素分泌过多引起的。我们报告一例异位分泌促肾上腺皮质激素(ACTH)的肝脏神经内分泌肿瘤病例。一名71岁女性,有直肠鳞癌病史,出现疲劳和全身弥漫性肿胀。肝脏活检显示为转移性神经内分泌癌。检查发现晨起皮质醇和ACTH水平显著升高。过夜地塞米松抑制试验及活检中ACTH免疫染色阳性提示继发于伴有骨转移的神经内分泌性肝肿瘤的副肿瘤性库欣综合征。这解释了患者持续的全身性水肿、高血糖和电解质异常。尽管进行了多种干预措施,患者的临床状况仍恶化,最终死亡。