复发性自发性纵隔气肿合并神经性厌食症1例。

Keita Tokumitsu, Keiichiro Hatoyama, Yuka Kubota, Kengo Asami, Masayuki Ohsato, Michitaka Okamoto, Junko Takeuchi, Koji Yachimori
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引用次数: 0

摘要

在本案例中,受试者是一名患有肥胖恐惧症的31岁女性,她限制自己的能量摄入,并在暴饮暴食后反复引起呕吐和误用泻药,这导致她在大约5个月内体重突然减轻了29公斤。xx年1月,在其长子的推荐下,患者首次作为门诊患者在我精神科接受检查。诊断为神经性厌食症后,受试者接受门诊治疗;然而,在自我感知的体重或体型方面没有任何改善,并且受试者表达了减肥的愿望。xx年5月,受试者自诉胸痛、咽痛、自吐后呼吸窘迫,在精神科门诊接受检查。胸部x线及CT显示纵隔气肿及皮下肺气肿。怀疑自发性食管破裂,这是一种致命的情况,因此,该对象被转移到能够进行食管手术的更先进的医疗机构。入院后,根据上消化道食管造影结果排除自发性食管破裂,诊断为自发性纵隔气肿。保守治疗后膈肌消失;然而,大约8个月后,自发性纵隔气肿复发,并伴有自我诱导的呕吐。对于饮食失调和自我诱导呕吐的患者,我们认为呕吐可引起纵隔气肿,并且假设持续或重新开始呕吐可能增加纵隔气肿复发的风险。因此,我们报告复发性肺膈作为一种由自我诱导的呕吐引起的生理并发症,在精神科的临床实践中应予以注意。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[A Case of Recurrent Spontaneous Pneumomediastinum with Anorexia Nervosa].

In the present case, the subject was a 31-year-old woman with obesophobia who restricted her energy intake and repeatedly induced vomiting and misused laxatives after binge eating, which caused a sudden weight loss of 29 kg in approximately 5 months. In January 20XX, the subject was first examined as an outpatient at our psychiatric department at the recommendation of her eldest son. Upon diagnosis of anorexia nervosa, the subject underwent outpatient treatment ; however, there was no improvement in the disturbance in self-per- ceived weight or shape, and the subject voiced her desire to lose weight. In May 20XX, the subject complained of chest pain, pharyngeal pain, and respiratory distress after self-induced vomiting and was, thus, examined at the psychiatric outpatient services. Chest X-ray and chest CT revealed pneumomediastinum and subcutaneous emphysema. Spontaneous oesophageal rupture, a fatal condition, was suspected and, therefore, the subject was transferred to a more advanced medical institution capable of esophageal surgery. After admission, spontane- ous oesophageal rupture was ruled out based on the results of upper gastrointestinal endos- copy with esophagography, and spontaneous pneumomediastinum was diagnosed. The pneu- momediastinum disappeared with conservative treatment ; however, after approximately 8 months, spontaneous pneumomediastinum recurred, following self-induced vomiting. For patients with eating disorders and who are involved in self-induce vomiting, we believe that the vomiting can cause pneumomediastinum, and it is assumed that continuation or recommencement of vomiting can potentially increase the risk that pneumomediastinum will recur. We, therefore, report recurring pneumoediastinum as a physical complication caused by self- induced vomiting that should be noted in clinical practice of the psychiatric department.

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