A Green Surprise: Bilateral Bilious Pleural Effusion Secondary to Esophageal Rupture-A Case Report.

IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL Journal of investigative medicine high impact case reports Pub Date : 2024-01-01 DOI:10.1177/23247096241231634
Diviya Bharathi Ravikumar, Barath Prashanth Sivasubramanian, Francis Vino Dominic Savio, Tharajan Gunendran, Saketh Palasamudram Shekar
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Abstract

Bilothorax, an exudative pleural effusion due to the accumulation of bile. It is also called cholethorax or thoracobilia and was initially reported in 1971. Here, we report a rare case of an elderly male presenting with bilateral bilothorax due to esophageal rupture. A 78-year-old man with multiple medical ailments presented to the emergency room (ER) with a severe episode of vomiting accompanied by a popping sound, respiratory distress, and right sided chest pain. The patient had tachycardia, BP of 101/89 mm Hg, and tachypnea. Computed tomography scan of the chest and abdomen revealed air adjacent to the esophagus, suggesting perforation, atelectasis of right lung, and bilateral pleural effusion (R > L). However, an esophagram did not reveal any perforation. Right-sided chest tube drained dark green bilious fluid. The day after admission, he experienced hemodynamic compromise and hypoxemia requiring intubation, along with fluids and inotropes support. Diagnosis of bilateral bilothorax complicated by hypoxemic respiratory failure with septic shock was made. Cultures were drawn, and empiric antibiotics were started. Nuclear hepatobiliary scan (HIDA) was performed to rule out a hepatobiliary fistula. Results showed reflux activity in the stomach, and distal esophageal leak was identified. Gastrojejunal stenting was performed. However, after prolonged intubation, the family decided on terminal extubation, and he died while receiving hospice care. This case highlights the rarity of bilateral bilothorax, where the HIDA scan played a crucial role in identifying an esophageal leak as the underlying cause, despite normal esophagram results. This condition necessitates prompt diagnosis and aggressive therapeutic interventions.

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绿色惊喜:食管破裂继发双侧双腔胸腔积液--病例报告。
胆胸(Bilothorax)是一种因胆汁积聚而引起的渗出性胸腔积液。它也被称为胆胸或胸腔积液,最初报道于 1971 年。在此,我们报告了一例因食管破裂导致双侧胆气胸的罕见老年男性病例。一名患有多种疾病的 78 岁男性因严重呕吐、伴有爆裂声、呼吸困难和右侧胸痛来到急诊室(ER)。患者心动过速,血压 101/89 mm Hg,呼吸急促。胸部和腹部的计算机断层扫描显示食管附近有空气,提示食管穿孔、右肺无气淤血和双侧胸腔积液(R>L)。然而,食管造影并未发现任何穿孔。右侧胸管引流出深绿色胆汁样液体。入院第二天,他出现了血流动力学损害和低氧血症,需要插管、输液和肌力支持。诊断结果为双侧胆气胸并发低氧血症呼吸衰竭和脓毒性休克。对患者进行了培养,并开始使用经验性抗生素。为了排除肝胆瘘的可能性,医生进行了核素肝胆扫描(HIDA)。结果显示胃部有反流活动,并发现了远端食管漏。医生为患者进行了胃空肠支架植入术。然而,在长时间插管后,家属决定终末期拔管,他在接受临终关怀时死亡。本病例突显了双侧胆气胸的罕见性,尽管食管造影结果正常,但 HIDA 扫描在确定食管漏为根本原因方面发挥了关键作用。这种情况需要及时诊断和积极的治疗干预。
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来源期刊
CiteScore
1.90
自引率
0.00%
发文量
165
审稿时长
12 weeks
期刊介绍: The AFMR is committed to enhancing the training and career development of our members and to furthering its mission to facilitate the conduct of research to improve medical care. Case reports represent an important avenue for trainees (interns, residents, and fellows) and early-stage faculty to demonstrate productive, scholarly activity.
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