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2020, Number 1

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Cir Gen 2020; 42 (1)

Giant liver cyst consequent to severe abdominal trauma. Finding after 10 years. Literature review

Magaña-Mainero, Pablo1; Garay-Lechuga, Daniel1; Jiménez-Martínez, Rafael2; Vázquez-Minero, Juan Carlos3
Full text How to cite this article 10.35366/92707

DOI

DOI: 10.35366/92707
URL: https://dx.doi.org/10.35366/92707

Language: English/Spanish [Versi?n en espa?ol]
References: 11
Page: 19-23
PDF size: 264.93 Kb.


Key words:

Liver, post-traumatic, giant cyst.

ABSTRACT

Introduction: Abdominal trauma represents one of the most frequent reasons for admission to the emergency department. Hepatic trauma represents the main cause of death in closed abdominal trauma with rates as high as 15%. Hepatic cysts are the less frequent sequel. Objective: To present a rare case and a review of the literature. 40-year-old male with a history of a car accident that required surgery in which hepatic resection was performed. 10 years later, he is admitted in the emergency department with multiple contusions after the attack by third persons, during the radiologic approach a giant liver cyst is found. Material and methods: A review of the international literature was made through electronic search engines, obtaining only five original articles limited to case reports. Result: There's no algorithm to follow in the management of post-traumatic liver cyst given that the reported evidence is resumed to case reports without standardized approaches and particular managements of each case. Conclusions: Post-traumatic hepatic cysts represent a low percentage in the incidence of liver disease and invasive treatment is reserved for those patients who present local complications. In our case, the patient lacked symptoms or complications caused by the cyst despite the size and time of evolution.



INTRODUCTION

Hepatic trauma is frequent in both penetrating and blunt trauma; mortality in hepatic trauma depends on the degree of injury, with grade VI injuries being frequently fatal.1 Hepatic trauma usually has sequelae, among which are: biliary leakage, abscesses, ischemic necrosis, etc. Hepatic cysts are the least frequent sequelae.



CASE PRESENTATION

This is the case of a 40-year-old man with a history of a car accident 10 years prior to his admission. He required surgery for blunt abdominal trauma, with cholecystectomy and liver resection, the extent of which is unknown, as well as intestinal resection and repair of a femoral vascular lesion. This present time he was taken by paramedics to the emergency room after being assaulted by third parties. He presented multiple contusions in the head, thorax, abdomen, and thoracic limbs, after which he was run over by a car with the vehicle passing over his abdomen.

On admission he was anxious, alert, and oriented. His initial ATLS (Advanced Trauma Life Support) assessment revealed no hemodynamic compromise, no neurological deficit, thorax with dermabrasions, bilateral ventilated lung fields, and basal hypoventilation of the right hemithorax. The abdomen showed skin tire marks, and was soft, depressible with deep generalized tenderness on palpation, and peritoneal irritation signs in lower quadrants. His thoracic limbs had dermabrasions on both forearms. ATLS protocol films were taken. The chest X-ray (Figure 1) showed right hemithorax with elevation of the hemidiaphragm, without pneumothorax or pleural effusion. A primary FAST (Focused Abdominal Sonography for Trauma) was performed that revealed no fluid in the pericardium, hepatorenal, splenorenal or pelvic spaces. A simple and contrasted thoraco-abdominal-pelvic computed axial tomography scan was performed (Figures 2 and 3) in which an image compatible with a simple hepatic cyst of 12. 6 × 14.7 cm was seen.

Because of the tomographic finding associated to the giant hepatic cyst the patient remained under surveillance for 48 hours after his admission to the hospital. Control laboratory tests and imaging studies were performed (Figure 4) that showed no significant changes compared to those obtained during his admission. There was no evidence of hemorrhagic conversion of the hepatic cyst. At discharge, the patient showed symptomatologic improvement, without any other complications.



LITERATURE REVIEW

Cystic liver disease is of diverse origin and the differential diagnosis includes pathologies such as bacterial and parasitic abscesses, biliomas, cystadenomas, and cystadenocarcinomas. They can also be classified according to their origin as congenital or acquired. Among the acquired ones, traumatic and neoplastic disease represent the lowest percentage, leaving post-traumatic cysts as a described entity with a prevalence of less than 0.5%.2 Diagnosis is mainly achieved through trans-operative findings due to complications and the rest is incidentally diagnosed during imaging techniques.3 Treatment tends to be conservative; however, there is controversy regarding which one is the best treatment and its availability.4

A literature search was performed in PubMed database for original articles in Spanish and English languages with the words MESH in a crisscrossed form "Liver"[Mesh], "Cysts"[Mesh], "Post-traumatic"[Word] to review the literature in terms of incidence, diagnosis, etiopathogenesis, and treatment. Five original articles published between the years 1996 and 2015 were retrieved, all corresponding to case reports. A comparative table between them was created (Table 1).

The liver is the organ mainly involved in blunt abdominal trauma.5 Non-infectious liver cysts are an entity first described in 1937 by Sanders,6 of which the most common presentation is that of congenital origin; thus, acquired cysts secondary to traumatic injury represent the least frequent variety.7 There is a small number of cases described in the international literature, mainly from Asian countries and in pediatric patients. The most frequent location is in the right lobe and usually they occur as unilocular lesions. The incidental finding is the most frequent presentation with a history of trauma, due to the increasingly frequent non-surgical management of patients with grade IV and V liver injuries.4,6 However, other series have found no correlation between the degree of trauma and cyst formation.7 In our case there were no records detailing the degree of injury or the growth rate of the cyst, since the patient remained totally asymptomatic during 10 years prior to current admission, and it was only diagnosed as a finding following the abdominal trauma study protocol.

Cyst formation is secondary to traumatic injury causing leakage of bile and blood resulting in a pseudocyst (no epithelium). Bleeding is usually self-limiting through coagulation, while the flow of bile continues promoting thus the growth of the cyst.8 For this reason, symptoms are usually late.9 In our case, despite the size and time of evolution, the patient denied any symptomatology, and had it not been for the current incident, he would not have been diagnosed with this giant liver cyst.

The clinical presentation varies, as most resolve spontaneously and another percentage progress asymptomatically to ultimately cause compressive symptoms, in which case they require treatment.4 Despite this, complications such as obstructive jaundice, hemorrhagic shock and biliary peritonitis tend to be rare as in our case.

Spontaneous regression of post-traumatic cysts has been described;6 however, in the case of symptomatic cysts, among the therapeutic options is drainage with a high recurrence at two years. Likewise, it has been reported that once the contents of the fistula are drained, they usually resolve spontaneously.4 In the case of simple cysts, excision and unroofing are viable therapeutic options with a recurrence rate of 0-20% and a mortality rate of up to 5%. In the case of our patient, conservative treatment was chosen given the absence of symptoms and favorable evolution and no hemorrhagic conversion.

Post-traumatic liver cyst is linked to bile duct injury and another proportion is linked to cholecystectomy, but the etiology of most is linked to a history of trauma.



CONCLUSIONS

For giant liver cysts, the least morbid therapeutic option is percutaneous drainage, mainly indicated in patients with compressive symptoms at the abdominal level. There is no a defined algorithm for the diagnosis and treatment of these lesions within the current classifications; however, tomography scan represents, as in our case, the most efficient and accurate diagnostic tool.

Treatment is controversial and without well-defined indications, and surgical treatment is emphasized in all patients with compressive, painful, or gastrointestinal symptoms.


REFERENCES

  1. Badger SA, Barclay R, Campbell P, Mole DJ, Diamond T. Management of liver trauma. World J Surg. 2009; 33: 2522-2537.

  2. Chen BK, Gamagami RA, Kang J, Easter D, Lopez T. Symptomatic post-traumatic cyst of the liver: treatment by laparoscopic surgery. J Laparoendosc Adv Surg Tech A. 2001; 11: 41-42.

  3. Asuquo M, Nwagbara V, Agbor C, Otobo F, Omotoso A. Giant simple hepatic cyst: a case report and review of relevant literature. Afr Health Sci. 2015; 15: 293-298.

  4. Zinner M, Ashley JS. Maingot's abdominal operations. 12th edition. New York: McGraw Hill Professional; 2012.

  5. Sharma DD, Shukla AK, Chaturvedi V, Jangid M, Raipuria G. Post traumatic pseudocyst of liver. JCR. 2015; 5: 271-273.

  6. Chuang JH, Huang SC. Posttraumatic hepatic cyst--an unusual sequela of liver injury in the era of imaging. J Pediatr Surg. 1996; 31: 272-274.

  7. Sugimoto T, Yoshioka T, Sawada Y, Sugimoto H, Maemura K. Post-traumatic cyst of the liver found on CT scan--a new concept. J Trauma. 1982; 22: 797-800.

  8. Christopher F. Rupture of the liver. Ann Surg. 1936; 103: 461-463.

  9. Singh KK, Nizarudeen A, Sulfikar MS, Maheshwaran A, George D. Post-traumatic (haemorrhagic)liver cyst. Indian J Surg. 2013; 75: 425-427.

  10. Dalal S, Garg P, Rohilla P. Post-traumatic hepatic cyst: an unusual sequel of liver injury. Internet Journal of Surgery. 2008; 8: 1-3.

  11. Treede RD, Rief W, Barke A, Aziz Q, Bennett MI, Benoliel R, et al. A classification of chronic pain for ICD-11. Pain. 2015; 156: 1003-1007.



AFFILIATIONS

1 General Surgery, American British Cowdray Medical Center, I.A.P., Mexico City, Mexico.

2 General Surgery, Cruz Roja Mexicana, I.A.P., Mexico City, Mexico.

3 Cardio-Thoracic Surgey, Cruz Roja Mexicana, I.A.P., Mexico City, Mexico.



Ethical considerations and responsibility: Data privacy. In accordance with the protocols established at the authors\' work site, the authors declare that they have followed the protocols on patient data privacy while preserving their anonymity. The informed consent of the patient referred to in the article is in the possession of the author.

Funding: No financial support was received for this study.

Disclosure: The authors declare that they do not have conflict of interests in this study.



CORRESPONDENCE

Dr. Daniel Garay-Lechuga. E-mail: daniel_garay_@hotmail.com. ORCID: https://orcid.org/0000-0003-1759-5787




Received: 12/23/2018. Accepted: 08/13/2019

Figure 1
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Figure 3
Figure 4
Table 1

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Cir Gen. 2020;42