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Revista Española de Enfermedades Digestivas

Print version ISSN 1130-0108

Rev. esp. enferm. dig. vol.104 n.9 Madrid Sep. 2012

https://dx.doi.org/10.4321/S1130-01082012000900012 

LETTERS TO THE EDITOR

 

Spontaneous hemoperitoneum due to rupture of short gastric artery after vomiting

Hemoperitoneo espontáneo secundario a rotura de vasos gástricos breves

 

 


Key words: Spontaneous hemoperitoneum. Cocaine. Vomiting. Short gastric artery.

Palabras clave: Hemoperitoneo espontáneo. Cocaína. Vómito. Vasos gástricos breves.


 

Dear Editor,

We report a 25-year-old man who initially presented acute epigastric pain followed by vomiting after the ingestion of alcohol and cocaine. He denied having any significant medical history or having undergone any trauma. On arrival in the emergency room, he had upper abdominal pain but without any peritoneal sign. His biochemical profile showed 14,300 white blood cell and neutrophilia, and the blood hemoglobin level dropped from 11.4 to 7.3 g/L, hypotension and pallor skin. After stabilization of his vital sign in the Intensive Care Unit, he underwent ultrasonography and contrast-enhanced computed tomography (CT) of the abdomen (Fig. 1), which revealed a hematoma in the lesser sac, and massive fluid collection or bloody ascites was also found in subhepatic and Morrison's spaces. The patient underwent emergency exploratory laparotomy to stop the spontaneous bleeding from a small branch of the short gastric artery, which was ligated without complication, during the operation, 1500 mL bloody ascites was noted in the peritoneal space and 500 mL blood clot had impacted on the lesser sac. The patient received 4 U of packed red blood cells during the surgery and recovered uneventfully.

 

Discussion

Spontaneous rupture of short gastric vessel after vomit effort is an extremely rare event that can cause spontaneous hemoperitoneum. Bibliography is scare and only 5 cases have been reported in England, North America, Spain, Italy, and Taiwan (1-5). In the literature, there are numerous well documented causes of spontaneous hemoperitoneum such as: gynecological disorders (ectopic pregnancy rupture, uterine myomas and endometriosis), malignancy (GIST, hepatic or renal tumor), blunt trauma, aneurismal rupture (central or visceral), idiopathic, deep abdominal varices from portal hypertension or excessive anticoagulant treatment (4-7). It is important to know the cocaine consumption in our patient. The cocaine has sympathetic and toxic effects at the central nervous and cardiovascular systems, leading to vasoconstriction, convulsive crisis, hypertension, arritmias and bleeding. The combination of alcohol and cocaine tends to have more toxicity (8,9).

It is clinically manifested by acute anemia syndrome and hypovolemia associated with abdominal pain, without any trauma. The spontaneous hemoperitoneum is a life-threatening condition may prove fatal even if promptly diagnosed and appropriately treated thus surgical intervention is the mainstay of treatment (7,10). In our case, he was diagnosed with hemoperitoneum resulting in hemorrhagic shock due to the spontaneous rupture of a small branch of the short gastric artery. The patient underwent emergency exploratory laparotomy with a good outcome. In the previous literature, the vomited effort is related to the Mallory Weiss, Boerhaave syndrome or even the rectum muscles hematoma but we do not know other cases of spontaneous hemoperitoneum with gastric vessels avulsion after vomiting with or without alcohol and cocaine consumption. Thus far, this is the first case reported in Spain. In our case, it is possible that cocaine hypertensive effect potentiated by the patient's emesis, increased stress on the splachnic vessels, resulting in spontaneous intra-abdominal hemorrhage. Therefore, we can say that hemoperitoneum should be considered in the differential diagnosis of acute abdominal pain in cocaine abusers (1-3,5,8,9).

Article funded in part by the FFIS (Foundation for Health Research and Training in the Region of Murcia, Spain, Group FFIS-008).

 

Ma Luisa García-García, Joana Miguel-Perelló, José Andrés García-Marín,
Germán Morales-Cuenca, Antonio Coll-Salinas and José Luis Aguayo-Albasini

Department of General Surgery. Hospital General Universitario Morales Meseguer.
School of Medicine. Campus de Excelencia Internacional "Campus Mare Nostrum".
Universidad de Murcia. Spain

 

References

1. Kaplan JL, Hausmann MG. Hemoperitoneum secondary to avulsed short gastric arteries after vomiting: the first documented case in North America. Curr Surg 2005;62:57-8.         [ Links ]

2. Hayes N, Waterworth PD, Griffin SM. Avulsion of short gastric arteries caused by vomiting. Gut 1994;35:1137-8.         [ Links ]

3. Piccagliani L, D'Arienzo M, Manco G, Luppi D, Rossi A. Haemoperitoneum secondary to avulsed short gastric arteries after vomiting. Chir Ital 2009;61:237-40.         [ Links ]

4. Rodero C, Moya A, Bueno JA, Planells M, Monzo A. Gravidic emesis causing massive intra-abdominal haemorrhage from an avulsed short gastric vessel. Eur J Obstet Gynecol Reprod Biol 2006;124:120-1.         [ Links ]

5. Ho MP, Chang CJ, Huang CY, Yu CJ, Tsai KC, Chen HA, et al. Spontaneous rupture of the short gastric artery after vomiting. Am J Emerg Med 2012;30:513 e1-3.         [ Links ]

6. Lucey BC, Varghese JC, Soto JA. Spontaneous hemoperitoneum: causes and significance. Curr Probl Diagn Radiol 2005;34:182-95.         [ Links ]

7. Cawyer JC, Stone CK. Abdominal apoplexy: a case report and review. J Emerg Med 2011;40:e49-52.         [ Links ]

8. Moreno Gallego A, Aguayo JL, Flores B, Soria T, Hernández Q, Ortiz, González-Costea R, et al. Ultrasonography and computed tomography reduce unnecessary surgery in abdominal rectus sheath haematoma. Br J Surg 1997;84:1295-7.         [ Links ]

9. Lingamfelter DC, Knight LD. Sudden death from massive gastrointestinal hemorrhage associated with crack cocaine use: case report and review of the literature. Am J Forensic Med Pathol 2010;31:98-9.         [ Links ]

10. de Magnée C, Feron P, Mehdi A. Haemoperitoneum associated with cocaine abuse: a case report. Acta Chir Belg 2007;107:690-2.         [ Links ]

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