2015, Number 4
<< Back Next >>
Ann Hepatol 2015; 14 (4)
Spontaneous hepatic rupture during pregnancy in a patient with peliosis hepatis
Cimbanassi S, Aseni P, Mariani A, Sammartano F, Bonacina E, Chiara O
Language: English
References: 25
Page: 553-558
PDF size: 151.12 Kb.
ABSTRACT
Spontaneous hepatic rupture (SHR) during pregnancy is a rare but well known complication and it usually
occurs alongside eclampsia or HELLP syndrome. SHR in uncomplicated pregnancy is extremely rare and can
be associated to different undiagnosed pathological conditions. We report the case of a nulliparous
woman, 27 weeks pregnant, with a peliosis hepatis, previously unknown, who was admitted to our unit due
to SHR and massive hemoperitoneum. The conception was obtained by embryo transfer after multiple
attempts of hormone-supported cycles using estrogens and progesterone. After emergency laparotomy
the patient was submitted to deliver of the dead foetus and damage control of the hepatic bleeding
source. At relaparotomy a right posterior sectionectomy (segments VI and VII) and segmentectomy of segment
V were performed. The patient was discharged in good physical conditions after 18 days from admission.
If hepatic rupture is suspected in a pregnant patient a collaborative multidisciplinary approach is
mandatory. The cornerstones of medical and surgical management are highlighted. At the best of our
knowledge this is the first case of SHR in a pregnant woman with peliosis hepatis. A possible correlation
of an increased risk for SHR in a pregnant patient who was submitted to several attempts for embryo
transfer is discussed. The relevant scientific literature of the possible causative role of the estrogen therapy
in inducing politic liver damage is also reviewed.
REFERENCES
Kelly J, Ryan DJ, O’Brien N, Kirwan WO. Second trimester hepatic rupture in a 35 year old nulliparous woman with HELLP syndrome: a case report. World Journal of Emergency Surgery 2009; 4: 23-7.
Matheï J, Janssen A, Olivier F, Depuydt P, Parmentier L, Harake R. Spontaneous postpartum subcapsular liver rupture. Acta Chir Belg. 2007; 107: 713-15.
Miguelote RF, Costa V, Vivas J, Gonzaga L, Menezes CA. Postpartum spontaneous rupture of a liver hematoma associated with preeclampsia and HELLP syndrome. Arch Gynecol Obstet 2009; 279: 923-6.
Marsh FA, Kaufmann SJ, Bhabra K. Surviving hepatic rupture in pregnancy-a literature review with an illustrative case report. J Obstet Gynecol 2003; 23: 109-13.
Sutton BC, Dunn ST, Landrum J, Mielke G: Fatal Postpartum Spontaneous Liver Rupture: Case Report and Literature Review. J Forensic Sci 2008; 53: 472-5.
Poo JL, Gongora J. Hepatic hematoma and hepatic rupture in pregnancy. Ann Hepatology 2006; 5: 224-6.
Fat BC, Terzibachian JJ, Grisey A, Houzé JP, Faller JP, Leung F, de Lapparent T, et al. Spontaneous hepatic rupture during an uncomplicated twin pregnancy. Gynecol Obstet Fertil 2011; 39: 7-10.
Hay JE. Liver disease in pregnancy. Hepatology 2008; 47: 1067-76.
Lee NM, Brady CW. Liver disease in pregnancy. World J Gastroenterol. 2009; 15: 897-906.
Grezzi F, Cromi A, Uccella S, Raio L, Bolis P, Surbek D. The Hayman technique: a simple method to treat postpartum haemorrhage. BJOG 2007; 114: 362-5.
Abercrombie J. Hemorrhage of the liver. London Medical Gazette 1844; 34: 792-4.
Abdi S, Cameron IC, Nakielny RA, Majeed AW. Spontaneous hepatic rupture and maternal death following an uncomplicated pregnancy and delivery. Br J Ostet Gynecol 2001; 108: 431-3.
Chen ZY, Qi OH, Dong ZL. Etiology and management of hemmorrhage in spontaneous liver rupture: a report of 70 cases. World J Gastroenterol 2002; 8: 1063-6.
Kou T, Watanabe M, Yazumi S. Hepatic Failure During Anabolic Steroid Therapy. Gastroenterology 2012; 143: 11-12.
Mascarenhas R, Mathias J, Varadarajan R, Geoghegan J, Traynor O. Spontaneous hepatic rupture: a report of five cases. HPB (Oxford) 2002; 4: 167-70.
Battula N, Tsapralis D, Takhar A, Coldham C, Mayer D, Isaac J, Muiesan P, et al. Aetio-pathogenesis and the management of spontaneous liver bleeding in the West: a 16- year single-centre experience. HPB (Oxford) 2012; 14: 382-9.
Tsokos M, Erbersdobl A. Pathology of peliosis. Forensic Science International 2005; 149: 25-33.
Sommacale D, Palladino E, Tambya EL, Dieboldb, Kianmanesha AR. Spontaneous hepatic rupture in a patient with peliosis hepatis: A report of one case. International Journal of Surgery Case Reports 2013; 4: 508-10.
Choi SK, Jin JS, Cho SG, Choi Sg, Kim CS, Choe YM, Lee KY, et al. Spontaneous liver rupture in a patient with peliosis hepatis: A case report. World J Gastroenterol 2009; 15: 5493-7.
Henny CP, Lim AE, Brummelkamp WH, Buller HR, Ten Cate JW. A review of the importance of acute multidisciplinary treatment following spontaneous rupture of the liver capsula during pregnancy. Surg Gynecol Obstet 1982; 156: 593-8.
Saadoun D, Cazals-Hatem D, Denninger M-H, Boudaoud L, Pham BN, Mallet V, Condat B, et al. Association of idiopathic hepatic sinusoidal dilatation with the immunological features of the antiphospholipid. Gut 2004; 53: 1516-19.
Staub PG, Leibowitz CB. Peliosis hepatis associated with oral contraceptive use. Australasian Radiology 1996; 40: 172-4.
van Erpecum KJ, Janssens AR, Kreuning J, Ruiter DJ, Kroon HM, Grond AJ. Generalized peliosis hepatis and cirrhosis after long-term use of oral contraceptives. Am J Gastroenterol 1988; 83: 572-5.
Perarnau JM, Bacq Y. Hepatic vascular involvement related to pregnancy, oral contraceptives, and estrogen replacement therapy. Semin Liver Dis 2008; 28: 315-27.
Huang CY, Wang ZW. Peliosis hepatis mimicking hepatic malignancy: A case report. Journal of Digestive Diseases 2013; 14: 272-5.