Literature DB >> 32110663

Ruptured splenic peliosis in a patient with no comorbidity: A case report.

Jiyoung Rhu1, Jinbeom Cho2.   

Abstract

BACKGROUND: Splenic peliosis is a disease characterized by widespread blood-filled cystic cavities within the parenchyma. Patients with this disease are usually asymptomatic; therefore, spontaneous or trauma-related rupture of the hemorrhagic cysts can occasionally cause life-threatening hemorrhagic shock. CASE
SUMMARY: A 51-year-old male patient with abdominal pain visited our emergency medical center two times with an interval of 2 mo. The patient was discharged from the hospital without treatment at his first visit; however, at the time of second admission, the hemoperitoneum with multiple cystic lesions of the spleen was found incidentally on the abdomen computed tomography scan. Since the patient was stable hemodynamically, a scheduled surgery was performed. The operative findings were consistent with splenic peliosis, and laparoscopic splenectomy was performed to prevent recurrent rupture of the hemorrhagic cysts.
CONCLUSION: Splenic peliosis is extremely rare, and we suggest splenectomy is necessarily required as a definite treatment for ruptured splenic peliosis to rescue patients with hemodynamic instability and to prevent recurrent rupture of hemorrhagic cysts in patients with stable hemodynamics. ©The Author(s) 2020. Published by Baishideng Publishing Group Inc. All rights reserved.

Entities:  

Keywords:  Case report; Hemodynamic instability; Hemorrhagic cysts; Peliosis; Spleen; Splenectomy

Year:  2020        PMID: 32110663      PMCID: PMC7031832          DOI: 10.12998/wjcc.v8.i3.535

Source DB:  PubMed          Journal:  World J Clin Cases        ISSN: 2307-8960            Impact factor:   1.337


  11 in total

Review 1.  Spleen: A new role for an old player?

Authors:  Giovanni Tarantino; Silvia Savastano; Domenico Capone; Annamaria Colao
Journal:  World J Gastroenterol       Date:  2011-09-07       Impact factor: 5.742

Review 2.  Peliosis of the spleen with massive recurrent haemorrhagic ascites, despite splenectomy, and associated with elevated levels of vascular endothelial growth factor.

Authors:  Franklin Joseph; Navid Younis; Geoffery Haydon; David H Adams; Siann Wynne; Martin B Gillet; Yasmine M Maurice; Mark E Lipton; David Berstock; Ian R Jones
Journal:  Eur J Gastroenterol Hepatol       Date:  2004-11       Impact factor: 2.566

3.  Isolated splenic peliosis presenting with giant splenomegaly and severe coagulopathy.

Authors:  Kensuke Adachi; Mitsuhito Ui; Hiroyuki Nojima; Yukari Takada; Kazuaki Enatsu
Journal:  Am J Surg       Date:  2011-08       Impact factor: 2.565

Review 4.  Peliosis of the spleen. Report of a case associated with chronic myelomonocytic leukemia, presenting with spontaneous splenic rupture.

Authors:  J Diebold; J Audouin
Journal:  Am J Surg Pathol       Date:  1983-03       Impact factor: 6.394

Review 5.  Splenic peliosis: a rare complication following liver transplantation.

Authors:  R Raghavan; S Alley; O Tawfik; P Webb; J Forster; M Uhl
Journal:  Dig Dis Sci       Date:  1999-06       Impact factor: 3.199

Review 6.  Pathology of peliosis.

Authors:  Michael Tsokos; Andreas Erbersdobler
Journal:  Forensic Sci Int       Date:  2005-04-20       Impact factor: 2.395

Review 7.  Laparoscopic splenectomy.

Authors:  N Katkhouda; E Mavor
Journal:  Surg Clin North Am       Date:  2000-08       Impact factor: 2.741

8.  Spontaneous splenic rupture due to isolated splenic peliosis.

Authors:  J P Celebrezze; D J Cottrell; G B Williams
Journal:  South Med J       Date:  1998-08       Impact factor: 0.954

9.  Peliosis hepatis. An unusual case involving multiple organs.

Authors:  K Ichijima; Y Kobashi; H Yamabe; Y Fujii; Y Inoue
Journal:  Acta Pathol Jpn       Date:  1980-01

Review 10.  Peliosis hepatis: Personal experience and literature review.

Authors:  Daniele Crocetti; Andrea Palmieri; Giuseppe Pedullà; Vittorio Pasta; Valerio D'Orazi; Gian Luca Grazi
Journal:  World J Gastroenterol       Date:  2015-12-14       Impact factor: 5.742

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