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嗜铬细胞瘤的不寻常表现:十三年焦虑症需精神科治疗。

Unusual presentation of pheochromocytoma: thirteen years of anxiety requiring psychiatric treatment.

作者信息

Alguire Catherine, Chbat Jessica, Forest Isabelle, Godbout Ariane, Bourdeau Isabelle

机构信息

Division of Endocrinology, Department of Medicine and Research Center (CRCHUM), Centre hospitalier de l'Université de Montréal, Montreal, Québec, Canada.

Department of Psychiatry, Centre hospitalier Pierre-Le Gardeur, Terrebonne, Québec, Canada.

出版信息

Endocrinol Diabetes Metab Case Rep. 2018 Apr 6;2018. doi: 10.1530/EDM-17-0176. eCollection 2018.

Abstract

UNLABELLED

Pheochromocytoma is a rare tumor of the adrenal gland. It often presents with the classic triad of headache, palpitations and generalized sweating. Although not described as a typical symptom of pheochromocytoma, anxiety is the fourth most common symptom reported by patients suffering of pheochromocytoma. We report the case of a 64 year old man who had severe anxiety and panic disorder as presenting symptoms of pheochromocytoma. After 13 years of psychiatric follow-up, the patient was diagnosed with malignant pheochromocytoma. After surgical resection of his pheochromocytoma and his hepatic metastases, the major panic attacks completely disappeared, the anxiety symptoms improved significantly and the psychiatric medications were stopped except for a very low maintenance dose of venlafaxine. We found in our cohort of 160 patients with pheochromocytoma 2 others cases of apparently benign tumors with severe anxiety that resolved after pheochromocytoma resection. These cases highlight that pheochromocytoma should be included in the differential diagnosis of refractory anxiety disorder.

LEARNING POINTS

Anxiety and panic disorder may be the main presenting symptoms of pheochromocytoma.The diagnosis of pheochromocytoma should be excluded in cases of long-term panic disorder refractory to medications since the anxiety may be secondary to a catecholamine-secreting tumor.Surgical treatment of pheochromocytoma leads to significant improvement of anxiety disorders.

摘要

未标注

嗜铬细胞瘤是一种罕见的肾上腺肿瘤。它常表现为头痛、心悸和全身出汗的典型三联征。尽管焦虑未被描述为嗜铬细胞瘤的典型症状,但它是嗜铬细胞瘤患者报告的第四大常见症状。我们报告一例64岁男性病例,其以严重焦虑和惊恐障碍作为嗜铬细胞瘤的首发症状。经过13年的精神科随访,该患者被诊断为恶性嗜铬细胞瘤。在手术切除其嗜铬细胞瘤及其肝转移灶后,主要的惊恐发作完全消失,焦虑症状显著改善,除了极低剂量维持治疗的文拉法辛外,精神科药物均停用。我们在160例嗜铬细胞瘤患者队列中发现另外2例明显为良性肿瘤但伴有严重焦虑的病例,在嗜铬细胞瘤切除后焦虑症状缓解。这些病例突出表明,嗜铬细胞瘤应纳入难治性焦虑症的鉴别诊断中。

学习要点

焦虑和惊恐障碍可能是嗜铬细胞瘤的主要首发症状。对于药物治疗难治的长期惊恐障碍病例,应排除嗜铬细胞瘤的诊断,因为焦虑可能继发于分泌儿茶酚胺的肿瘤。嗜铬细胞瘤的手术治疗可显著改善焦虑症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf87/5890079/911e596f58f2/edmcr-2018-170176-g001.jpg

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