嗜铬细胞瘤合并肝脓肿及假性肠梗阻1例。

IF 3.9 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM Therapeutic Advances in Endocrinology and Metabolism Pub Date : 2022-01-01 DOI:10.1177/20420188221139652
Mikiko Okazaki-Hada, Izumi Fukuda, Ryuta Nagaoka, Mototsugu Nagao, Takehito Igarashi, Shunsuke Kobayashi, Takeshi Oba, Yuji Yamaguchi, Tomoko Nagamine, Iwao Sugitani, Hitoshi Sugihara
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摘要

嗜铬细胞瘤可表现为多种症状。嗜铬细胞瘤的非特异性表现包括肠假性梗阻和体重减轻。在此,我们报告一个嗜铬细胞瘤的病例,其中由于过量的儿茶酚胺而导致的长期肠道假性阻塞是导致肝脓肿发展的因素之一。患者男,18岁,有癫痫持续状态史,严重智力障碍,因发热、便秘2个月入院检查。入院时发热,体重指数9.5 kg/m2。经全面检查病人的发烧情况,血培养结果显示拟杆菌阳性。计算机断层扫描显示假性肠梗阻和肝脏低密度区提示肝脓肿。影像学检查还显示右侧肾上腺肿块,内分泌检查显示血浆去甲肾上腺素和尿去甲肾上腺素水平升高。另外,右肾上腺肿块在123I-metaiodobenzylguanidine显像上显示摄取。这些结果明确诊断为嗜铬细胞瘤。患者最终被诊断为嗜铬细胞瘤并发肝脓肿。经抗生素及超声引导引流治疗肝脓肿后,行肾上腺切除术。病理表现符合嗜铬细胞瘤。术后儿茶酚胺过量恢复正常,假性肠梗阻改善,体重减轻。我们怀疑长时间的肠道假性梗阻导致细菌移位和肝脓肿的发展。据我们所知,这是首例嗜铬细胞瘤合并肝脓肿的报告。此外,该患者的临床表现与嗜铬细胞瘤不同,患者没有高血压、心动过速等典型症状,而是出现便秘、假性肠梗阻、体重减轻等症状。本病例为儿茶酚胺过量对肠道和体重的影响提供了有价值的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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A case of pheochromocytoma associated with liver abscess and intestinal pseudo-obstruction.

Pheochromocytomas can present with various symptoms. Nonspecific manifestations of pheochromocytoma include intestinal pseudo-obstruction and weight loss. Here, we present a case of pheochromocytoma in which prolonged intestinal pseudo-obstruction due to excess catecholamines was one of the factors leading to the development of a liver abscess. An 18-year-old male patient with a history of status epilepticus and severe intellectual disability was transferred to our hospital for a thorough examination of fever and constipation that had lasted for 2 months. When admitted to our hospital, he had fever, and his body mass index was 9.5 kg/m2. Upon comprehensive examination of the patient's fever, the blood culture was found positive for Bacteroides. Computed tomography showed findings of intestinal pseudo-obstruction and a low density region in the liver that indicated a liver abscess. Imaging studies also revealed a right adrenal mass and endocrinological test showed elevated plasma norepinephrine and urine normetanephrine levels. In addition, the right adrenal mass showed uptake on 123I-metaiodobenzylguanidine scintigraphy. These findings led to a definite diagnosis of pheochromocytoma. The patient was eventually diagnosed with a pheochromocytoma coexisting with a liver abscess. After treating the liver abscess with antibiotics and ultrasound-guided drainage, an adrenalectomy was performed. The pathological findings were consistent with pheochromocytoma. Postoperatively, the catecholamine excess normalized and intestinal pseudo-obstruction and weight loss improved. We suspected that prolonged intestinal pseudo-obstruction resulted in bacterial translocation and development of a liver abscess. To the best of our knowledge, this is the first report of a pheochromocytoma associated with a liver abscess. Moreover, the clinical presentation of this patient was unusual for pheochromocytoma, as the patient did not have typical symptoms such as hypertension or tachycardia, but rather presented with constipation, intestinal pseudo-obstruction, and weight loss. This case provides valuable insight regarding the impact of catecholamine excess on the intestinal tract and body weight.

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来源期刊
Therapeutic Advances in Endocrinology and Metabolism
Therapeutic Advances in Endocrinology and Metabolism Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
7.70
自引率
2.60%
发文量
42
审稿时长
8 weeks
期刊介绍: Therapeutic Advances in Endocrinology and Metabolism delivers the highest quality peer-reviewed articles, reviews, and scholarly comment on pioneering efforts and innovative studies across all areas of endocrinology and metabolism.
期刊最新文献
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